Genome-wide comparison of microRNAs and their targeted transcripts among leaf, flower and fruit of sweet orange
Identifieur interne : 000574 ( Pmc/Corpus ); précédent : 000573; suivant : 000575Genome-wide comparison of microRNAs and their targeted transcripts among leaf, flower and fruit of sweet orange
Auteurs : Yuanlong Liu ; Lun Wang ; Dijun Chen ; Xiaomeng Wu ; Ding Huang ; Lingling Chen ; Li Li ; Xiuxin Deng ; Qiang XuSource :
- BMC Genomics [ 1471-2164 ] ; 2014.
Abstract
In plants, microRNAs (miRNAs) regulate gene expression mainly at the post-transcriptional level. Previous studies have demonstrated that miRNA-mediated gene silencing pathways play vital roles in plant development. Here, we used a high-throughput sequencing approach to characterize the miRNAs and their targeted transcripts in the leaf, flower and fruit of sweet orange.
A total of 183 known miRNAs and 38 novel miRNAs were identified. An in-house script was used to identify all potential secondary siRNAs derived from miRNA-targeted transcripts using sRNA and degradome sequencing data. Genome mapping revealed that these miRNAs were evenly distributed across the genome with several small clusters, and 69 pre-miRNAs were co-localized with simple sequence repeats (SSRs). Noticeably, the loop size of pre-miR396c was influenced by the repeat number of CUU unit. The expression pattern of miRNAs among different tissues and developmental stages were further investigated by both qRT-PCR and RNA gel blotting. Interestingly, Csi-miR164 was highly expressed in fruit ripening stage, and was validated to target a NAC transcription factor. This study depicts a global picture of miRNAs and their target genes in the genome of sweet orange, and focused on the comparison among leaf, flower and fruit tissues.
This study provides a global view of miRNAs and their target genes in different tissue of sweet orange, and focused on the identification of miRNA involved in the regulation of fruit ripening. The results of this study lay a foundation for unraveling key regulators of orange fruit development and ripening on post-transcriptional level.
The online version of this article (doi:10.1186/1471-2164-15-695) contains supplementary material, which is available to authorized users.
Url:
DOI: 10.1186/1471-2164-15-695
PubMed: 25142253
PubMed Central: 4158063
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PMC:4158063Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Genome-wide comparison of microRNAs and their targeted transcripts among leaf, flower and fruit of sweet orange</title>
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<author><name sortKey="Chen, Dijun" sort="Chen, Dijun" uniqKey="Chen D" first="Dijun" last="Chen">Dijun Chen</name>
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<author><name sortKey="Deng, Xiuxin" sort="Deng, Xiuxin" uniqKey="Deng X" first="Xiuxin" last="Deng">Xiuxin Deng</name>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>In plants, microRNAs (miRNAs) regulate gene expression mainly at the post-transcriptional level. Previous studies have demonstrated that miRNA-mediated gene silencing pathways play vital roles in plant development. Here, we used a high-throughput sequencing approach to characterize the miRNAs and their targeted transcripts in the leaf, flower and fruit of sweet orange.</p>
</sec>
<sec><title>Results</title>
<p>A total of 183 known miRNAs and 38 novel miRNAs were identified. An in-house script was used to identify all potential secondary siRNAs derived from miRNA-targeted transcripts using sRNA and degradome sequencing data. Genome mapping revealed that these miRNAs were evenly distributed across the genome with several small clusters, and 69 pre-miRNAs were co-localized with simple sequence repeats (SSRs). Noticeably, the loop size of pre-miR396c was influenced by the repeat number of CUU unit. The expression pattern of miRNAs among different tissues and developmental stages were further investigated by both qRT-PCR and RNA gel blotting. Interestingly, Csi-miR164 was highly expressed in fruit ripening stage, and was validated to target a NAC transcription factor. This study depicts a global picture of miRNAs and their target genes in the genome of sweet orange, and focused on the comparison among leaf, flower and fruit tissues.</p>
</sec>
<sec><title>Conclusions</title>
<p>This study provides a global view of miRNAs and their target genes in different tissue of sweet orange, and focused on the identification of miRNA involved in the regulation of fruit ripening. The results of this study lay a foundation for unraveling key regulators of orange fruit development and ripening on post-transcriptional level.</p>
</sec>
<sec><title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/1471-2164-15-695) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wang, H" uniqKey="Wang H">H Wang</name>
</author>
<author><name sortKey="Zhang, X" uniqKey="Zhang X">X Zhang</name>
</author>
<author><name sortKey="Liu, J" uniqKey="Liu J">J Liu</name>
</author>
<author><name sortKey="Kiba, T" uniqKey="Kiba T">T Kiba</name>
</author>
<author><name sortKey="Woo, J" uniqKey="Woo J">J Woo</name>
</author>
<author><name sortKey="Ojo, T" uniqKey="Ojo T">T Ojo</name>
</author>
<author><name sortKey="Hafner, M" uniqKey="Hafner M">M Hafner</name>
</author>
<author><name sortKey="Tuschl, T" uniqKey="Tuschl T">T Tuschl</name>
</author>
<author><name sortKey="Chua, Nh" uniqKey="Chua N">NH Chua</name>
</author>
<author><name sortKey="Wang, Xj" uniqKey="Wang X">XJ Wang</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Kim, Vn" uniqKey="Kim V">VN Kim</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Jin, Hl" uniqKey="Jin H">HL Jin</name>
</author>
<author><name sortKey="Zhang, Xm" uniqKey="Zhang X">XM Zhang</name>
</author>
<author><name sortKey="Zhao, Hw" uniqKey="Zhao H">HW Zhao</name>
</author>
<author><name sortKey="Gao, S" uniqKey="Gao S">S Gao</name>
</author>
<author><name sortKey="Wang, Wc" uniqKey="Wang W">WC Wang</name>
</author>
<author><name sortKey="Katiyar Agarwal, S" uniqKey="Katiyar Agarwal S">S Katiyar-Agarwal</name>
</author>
<author><name sortKey="Huang, Hd" uniqKey="Huang H">HD Huang</name>
</author>
<author><name sortKey="Raikhel, N" uniqKey="Raikhel N">N Raikhel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Chen, Hm" uniqKey="Chen H">HM Chen</name>
</author>
<author><name sortKey="Chen, Lt" uniqKey="Chen L">LT Chen</name>
</author>
<author><name sortKey="Patel, K" uniqKey="Patel K">K Patel</name>
</author>
<author><name sortKey="Li, Yh" uniqKey="Li Y">YH Li</name>
</author>
<author><name sortKey="Baulcombe, Dc" uniqKey="Baulcombe D">DC Baulcombe</name>
</author>
<author><name sortKey="Wu, Sh" uniqKey="Wu S">SH Wu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Allen, E" uniqKey="Allen E">E Allen</name>
</author>
<author><name sortKey="Howell, Md" uniqKey="Howell M">MD Howell</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Axtell, Mj" uniqKey="Axtell M">MJ Axtell</name>
</author>
<author><name sortKey="Jan, C" uniqKey="Jan C">C Jan</name>
</author>
<author><name sortKey="Rajagopalan, R" uniqKey="Rajagopalan R">R Rajagopalan</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Axtell, Mj" uniqKey="Axtell M">MJ Axtell</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Karlova, R" uniqKey="Karlova R">R Karlova</name>
</author>
<author><name sortKey="Van Haarst, Jc" uniqKey="Van Haarst J">JC van Haarst</name>
</author>
<author><name sortKey="Maliepaard, C" uniqKey="Maliepaard C">C Maliepaard</name>
</author>
<author><name sortKey="Van De Geest, H" uniqKey="Van De Geest H">H van de Geest</name>
</author>
<author><name sortKey="Bovy, Ag" uniqKey="Bovy A">AG Bovy</name>
</author>
<author><name sortKey="Lammers, M" uniqKey="Lammers M">M Lammers</name>
</author>
<author><name sortKey="Angenent, Gc" uniqKey="Angenent G">GC Angenent</name>
</author>
<author><name sortKey="De Maagd, Ra" uniqKey="De Maagd R">RA de Maagd</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wang, C" uniqKey="Wang C">C Wang</name>
</author>
<author><name sortKey="Han, J" uniqKey="Han J">J Han</name>
</author>
<author><name sortKey="Liu, Ch" uniqKey="Liu C">CH Liu</name>
</author>
<author><name sortKey="Kibet, Kn" uniqKey="Kibet K">KN Kibet</name>
</author>
<author><name sortKey="Kayesh, E" uniqKey="Kayesh E">E Kayesh</name>
</author>
<author><name sortKey="Shangguan, Lf" uniqKey="Shangguan L">LF Shangguan</name>
</author>
<author><name sortKey="Li, Xy" uniqKey="Li X">XY Li</name>
</author>
<author><name sortKey="Fang, Jg" uniqKey="Fang J">JG Fang</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Aryal, R" uniqKey="Aryal R">R Aryal</name>
</author>
<author><name sortKey="Jagadeeswaran, G" uniqKey="Jagadeeswaran G">G Jagadeeswaran</name>
</author>
<author><name sortKey="Zheng, Y" uniqKey="Zheng Y">Y Zheng</name>
</author>
<author><name sortKey="Yu, Qy" uniqKey="Yu Q">QY Yu</name>
</author>
<author><name sortKey="Sunkar, R" uniqKey="Sunkar R">R Sunkar</name>
</author>
<author><name sortKey="Ming, R" uniqKey="Ming R">R Ming</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Xu, L" uniqKey="Xu L">L Xu</name>
</author>
<author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author><name sortKey="Xu, Yy" uniqKey="Xu Y">YY Xu</name>
</author>
<author><name sortKey="Wang, Lj" uniqKey="Wang L">LJ Wang</name>
</author>
<author><name sortKey="Zhai, Ll" uniqKey="Zhai L">LL Zhai</name>
</author>
<author><name sortKey="Zhu, Xw" uniqKey="Zhu X">XW Zhu</name>
</author>
<author><name sortKey="Gong, Yq" uniqKey="Gong Y">YQ Gong</name>
</author>
<author><name sortKey="Ye, S" uniqKey="Ye S">S Ye</name>
</author>
<author><name sortKey="Liu, Lw" uniqKey="Liu L">LW Liu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Zhang, X N" uniqKey="Zhang X">X-N Zhang</name>
</author>
<author><name sortKey="Li, X" uniqKey="Li X">X Li</name>
</author>
<author><name sortKey="Liu, J H" uniqKey="Liu J">J-H Liu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Meyers, Bc" uniqKey="Meyers B">BC Meyers</name>
</author>
<author><name sortKey="Axtell, Mj" uniqKey="Axtell M">MJ Axtell</name>
</author>
<author><name sortKey="Bartel, B" uniqKey="Bartel B">B Bartel</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
<author><name sortKey="Baulcombe, D" uniqKey="Baulcombe D">D Baulcombe</name>
</author>
<author><name sortKey="Bowman, Jl" uniqKey="Bowman J">JL Bowman</name>
</author>
<author><name sortKey="Cao, X" uniqKey="Cao X">X Cao</name>
</author>
<author><name sortKey="Carrington, Jc" uniqKey="Carrington J">JC Carrington</name>
</author>
<author><name sortKey="Chen, Xm" uniqKey="Chen X">XM Chen</name>
</author>
<author><name sortKey="Green, Pj" uniqKey="Green P">PJ Green</name>
</author>
<author><name sortKey="Griffiths Jones, S" uniqKey="Griffiths Jones S">S Griffiths-Jones</name>
</author>
<author><name sortKey="Jacobsen, Se" uniqKey="Jacobsen S">SE Jacobsen</name>
</author>
<author><name sortKey="Mallory, Ac" uniqKey="Mallory A">AC Mallory</name>
</author>
<author><name sortKey="Martienssen, Ra" uniqKey="Martienssen R">RA Martienssen</name>
</author>
<author><name sortKey="Poethig, Rs" uniqKey="Poethig R">RS Poethig</name>
</author>
<author><name sortKey="Qi, Y" uniqKey="Qi Y">Y Qi</name>
</author>
<author><name sortKey="Vaucheret, H" uniqKey="Vaucheret H">H Vaucheret</name>
</author>
<author><name sortKey="Voinnet, O" uniqKey="Voinnet O">O Voinnet</name>
</author>
<author><name sortKey="Watanabe, Y" uniqKey="Watanabe Y">Y Watanabe</name>
</author>
<author><name sortKey="Weigel, D" uniqKey="Weigel D">D Weigel</name>
</author>
<author><name sortKey="Zhu, Jk" uniqKey="Zhu J">JK Zhu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="German, Ma" uniqKey="German M">MA German</name>
</author>
<author><name sortKey="Pillay, M" uniqKey="Pillay M">M Pillay</name>
</author>
<author><name sortKey="Jeong, Dh" uniqKey="Jeong D">DH Jeong</name>
</author>
<author><name sortKey="Hetawal, A" uniqKey="Hetawal A">A Hetawal</name>
</author>
<author><name sortKey="Luo, S" uniqKey="Luo S">S Luo</name>
</author>
<author><name sortKey="Janardhanan, P" uniqKey="Janardhanan P">P Janardhanan</name>
</author>
<author><name sortKey="Kannan, V" uniqKey="Kannan V">V Kannan</name>
</author>
<author><name sortKey="Rymarquis, La" uniqKey="Rymarquis L">LA Rymarquis</name>
</author>
<author><name sortKey="Nobuta, K" uniqKey="Nobuta K">K Nobuta</name>
</author>
<author><name sortKey="German, R" uniqKey="German R">R German</name>
</author>
<author><name sortKey="De Paoli, E" uniqKey="De Paoli E">E De Paoli</name>
</author>
<author><name sortKey="Lu, C" uniqKey="Lu C">C Lu</name>
</author>
<author><name sortKey="Schroth, G" uniqKey="Schroth G">G Schroth</name>
</author>
<author><name sortKey="Meyers, Bc" uniqKey="Meyers B">BC Meyers</name>
</author>
<author><name sortKey="Green, Pj" uniqKey="Green P">PJ Green</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Addo Quaye, C" uniqKey="Addo Quaye C">C Addo-Quaye</name>
</author>
<author><name sortKey="Miller, W" uniqKey="Miller W">W Miller</name>
</author>
<author><name sortKey="Axtell, Mj" uniqKey="Axtell M">MJ Axtell</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="German, Ma" uniqKey="German M">MA German</name>
</author>
<author><name sortKey="Luo, S" uniqKey="Luo S">S Luo</name>
</author>
<author><name sortKey="Schroth, G" uniqKey="Schroth G">G Schroth</name>
</author>
<author><name sortKey="Meyers, Bc" uniqKey="Meyers B">BC Meyers</name>
</author>
<author><name sortKey="Green, Pj" uniqKey="Green P">PJ Green</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Garcia, D" uniqKey="Garcia D">D Garcia</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Chuck, G" uniqKey="Chuck G">G Chuck</name>
</author>
<author><name sortKey="O Connor, D" uniqKey="O Connor D">D O'Connor</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Juarez, Mt" uniqKey="Juarez M">MT Juarez</name>
</author>
<author><name sortKey="Kui, Js" uniqKey="Kui J">JS Kui</name>
</author>
<author><name sortKey="Thomas, J" uniqKey="Thomas J">J Thomas</name>
</author>
<author><name sortKey="Heller, Ba" uniqKey="Heller B">BA Heller</name>
</author>
<author><name sortKey="Timmermans, Mc" uniqKey="Timmermans M">MC Timmermans</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Schwab, R" uniqKey="Schwab R">R Schwab</name>
</author>
<author><name sortKey="Palatnik, Jf" uniqKey="Palatnik J">JF Palatnik</name>
</author>
<author><name sortKey="Riester, M" uniqKey="Riester M">M Riester</name>
</author>
<author><name sortKey="Schommer, C" uniqKey="Schommer C">C Schommer</name>
</author>
<author><name sortKey="Schmid, M" uniqKey="Schmid M">M Schmid</name>
</author>
<author><name sortKey="Weigel, D" uniqKey="Weigel D">D Weigel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Nikovics, K" uniqKey="Nikovics K">K Nikovics</name>
</author>
<author><name sortKey="Blein, T" uniqKey="Blein T">T Blein</name>
</author>
<author><name sortKey="Peaucelle, A" uniqKey="Peaucelle A">A Peaucelle</name>
</author>
<author><name sortKey="Ishida, T" uniqKey="Ishida T">T Ishida</name>
</author>
<author><name sortKey="Morin, H" uniqKey="Morin H">H Morin</name>
</author>
<author><name sortKey="Aida, M" uniqKey="Aida M">M Aida</name>
</author>
<author><name sortKey="Laufs, P" uniqKey="Laufs P">P Laufs</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Berger, Y" uniqKey="Berger Y">Y Berger</name>
</author>
<author><name sortKey="Harpaz Saad, S" uniqKey="Harpaz Saad S">S Harpaz-Saad</name>
</author>
<author><name sortKey="Brand, A" uniqKey="Brand A">A Brand</name>
</author>
<author><name sortKey="Melnik, H" uniqKey="Melnik H">H Melnik</name>
</author>
<author><name sortKey="Sirding, N" uniqKey="Sirding N">N Sirding</name>
</author>
<author><name sortKey="Alvarez, Jp" uniqKey="Alvarez J">JP Alvarez</name>
</author>
<author><name sortKey="Zinder, M" uniqKey="Zinder M">M Zinder</name>
</author>
<author><name sortKey="Samach, A" uniqKey="Samach A">A Samach</name>
</author>
<author><name sortKey="Eshed, Y" uniqKey="Eshed Y">Y Eshed</name>
</author>
<author><name sortKey="Ori, N" uniqKey="Ori N">N Ori</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Bertolini, E" uniqKey="Bertolini E">E Bertolini</name>
</author>
<author><name sortKey="Verelst, W" uniqKey="Verelst W">W Verelst</name>
</author>
<author><name sortKey="Horner, Ds" uniqKey="Horner D">DS Horner</name>
</author>
<author><name sortKey="Gianfranceschi, L" uniqKey="Gianfranceschi L">L Gianfranceschi</name>
</author>
<author><name sortKey="Piccolo, V" uniqKey="Piccolo V">V Piccolo</name>
</author>
<author><name sortKey="Inze, D" uniqKey="Inze D">D Inze</name>
</author>
<author><name sortKey="Pe, Me" uniqKey="Pe M">ME Pe</name>
</author>
<author><name sortKey="Mica, E" uniqKey="Mica E">E Mica</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Millar, Aa" uniqKey="Millar A">AA Millar</name>
</author>
<author><name sortKey="Gubler, F" uniqKey="Gubler F">F Gubler</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Palatnik, Jf" uniqKey="Palatnik J">JF Palatnik</name>
</author>
<author><name sortKey="Wollmann, H" uniqKey="Wollmann H">H Wollmann</name>
</author>
<author><name sortKey="Schommer, C" uniqKey="Schommer C">C Schommer</name>
</author>
<author><name sortKey="Schwab, R" uniqKey="Schwab R">R Schwab</name>
</author>
<author><name sortKey="Boisbouvier, J" uniqKey="Boisbouvier J">J Boisbouvier</name>
</author>
<author><name sortKey="Rodriguez, R" uniqKey="Rodriguez R">R Rodriguez</name>
</author>
<author><name sortKey="Warthmann, N" uniqKey="Warthmann N">N Warthmann</name>
</author>
<author><name sortKey="Allen, E" uniqKey="Allen E">E Allen</name>
</author>
<author><name sortKey="Dezulian, T" uniqKey="Dezulian T">T Dezulian</name>
</author>
<author><name sortKey="Huson, D" uniqKey="Huson D">D Huson</name>
</author>
<author><name sortKey="Carrington, Jc" uniqKey="Carrington J">JC Carrington</name>
</author>
<author><name sortKey="Weigel, D" uniqKey="Weigel D">D Weigel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Mathieu, J" uniqKey="Mathieu J">J Mathieu</name>
</author>
<author><name sortKey="Yant, Lj" uniqKey="Yant L">LJ Yant</name>
</author>
<author><name sortKey="Murdter, F" uniqKey="Murdter F">F Murdter</name>
</author>
<author><name sortKey="Kuttner, F" uniqKey="Kuttner F">F Kuttner</name>
</author>
<author><name sortKey="Schmid, M" uniqKey="Schmid M">M Schmid</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wu, G" uniqKey="Wu G">G Wu</name>
</author>
<author><name sortKey="Park, My" uniqKey="Park M">MY Park</name>
</author>
<author><name sortKey="Conway, Sr" uniqKey="Conway S">SR Conway</name>
</author>
<author><name sortKey="Wang, Jw" uniqKey="Wang J">JW Wang</name>
</author>
<author><name sortKey="Weigel, D" uniqKey="Weigel D">D Weigel</name>
</author>
<author><name sortKey="Poethig, Rs" uniqKey="Poethig R">RS Poethig</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gandikota, M" uniqKey="Gandikota M">M Gandikota</name>
</author>
<author><name sortKey="Birkenbihl, Rp" uniqKey="Birkenbihl R">RP Birkenbihl</name>
</author>
<author><name sortKey="Hohmann, S" uniqKey="Hohmann S">S Hohmann</name>
</author>
<author><name sortKey="Cardon, Gh" uniqKey="Cardon G">GH Cardon</name>
</author>
<author><name sortKey="Saedler, H" uniqKey="Saedler H">H Saedler</name>
</author>
<author><name sortKey="Huijser, P" uniqKey="Huijser P">P Huijser</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Zhang, Yc" uniqKey="Zhang Y">YC Zhang</name>
</author>
<author><name sortKey="Yu, Y" uniqKey="Yu Y">Y Yu</name>
</author>
<author><name sortKey="Wang, Cy" uniqKey="Wang C">CY Wang</name>
</author>
<author><name sortKey="Li, Zy" uniqKey="Li Z">ZY Li</name>
</author>
<author><name sortKey="Liu, Q" uniqKey="Liu Q">Q Liu</name>
</author>
<author><name sortKey="Xu, J" uniqKey="Xu J">J Xu</name>
</author>
<author><name sortKey="Liao, Jy" uniqKey="Liao J">JY Liao</name>
</author>
<author><name sortKey="Wang, Xj" uniqKey="Wang X">XJ Wang</name>
</author>
<author><name sortKey="Qu, Lh" uniqKey="Qu L">LH Qu</name>
</author>
<author><name sortKey="Chen, F" uniqKey="Chen F">F Chen</name>
</author>
<author><name sortKey="Xin, P" uniqKey="Xin P">P Xin</name>
</author>
<author><name sortKey="Yan, C" uniqKey="Yan C">C Yan</name>
</author>
<author><name sortKey="Chu, J" uniqKey="Chu J">J Chu</name>
</author>
<author><name sortKey="Li, Hq" uniqKey="Li H">HQ Li</name>
</author>
<author><name sortKey="Chen, Yq" uniqKey="Chen Y">YQ Chen</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author><name sortKey="Itaya, A" uniqKey="Itaya A">A Itaya</name>
</author>
<author><name sortKey="Zhong, Xh" uniqKey="Zhong X">XH Zhong</name>
</author>
<author><name sortKey="Wu, Y" uniqKey="Wu Y">Y Wu</name>
</author>
<author><name sortKey="Zhang, Jf" uniqKey="Zhang J">JF Zhang</name>
</author>
<author><name sortKey="Van Der Knaap, E" uniqKey="Van Der Knaap E">E van der Knaap</name>
</author>
<author><name sortKey="Olmstead, R" uniqKey="Olmstead R">R Olmstead</name>
</author>
<author><name sortKey="Qi, Yj" uniqKey="Qi Y">YJ Qi</name>
</author>
<author><name sortKey="Ding, Ba" uniqKey="Ding B">BA Ding</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Song, Cn" uniqKey="Song C">CN Song</name>
</author>
<author><name sortKey="Fang, Jg" uniqKey="Fang J">JG Fang</name>
</author>
<author><name sortKey="Li, Xy" uniqKey="Li X">XY Li</name>
</author>
<author><name sortKey="Liu, H" uniqKey="Liu H">H Liu</name>
</author>
<author><name sortKey="Chao, Ct" uniqKey="Chao C">CT Chao</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Song, Cn" uniqKey="Song C">CN Song</name>
</author>
<author><name sortKey="Wang, C" uniqKey="Wang C">C Wang</name>
</author>
<author><name sortKey="Zhang, Cq" uniqKey="Zhang C">CQ Zhang</name>
</author>
<author><name sortKey="Korir, Nk" uniqKey="Korir N">NK Korir</name>
</author>
<author><name sortKey="Yu, Hp" uniqKey="Yu H">HP Yu</name>
</author>
<author><name sortKey="Ma, Zq" uniqKey="Ma Z">ZQ Ma</name>
</author>
<author><name sortKey="Fang, Jg" uniqKey="Fang J">JG Fang</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Zhang, Jz" uniqKey="Zhang J">JZ Zhang</name>
</author>
<author><name sortKey="Ai, Xy" uniqKey="Ai X">XY Ai</name>
</author>
<author><name sortKey="Guo, Ww" uniqKey="Guo W">WW Guo</name>
</author>
<author><name sortKey="Peng, Sa" uniqKey="Peng S">SA Peng</name>
</author>
<author><name sortKey="Deng, Xx" uniqKey="Deng X">XX Deng</name>
</author>
<author><name sortKey="Hu, Cg" uniqKey="Hu C">CG Hu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Xu, Q" uniqKey="Xu Q">Q Xu</name>
</author>
<author><name sortKey="Liu, Yl" uniqKey="Liu Y">YL Liu</name>
</author>
<author><name sortKey="Zhu, Ad" uniqKey="Zhu A">AD Zhu</name>
</author>
<author><name sortKey="Wu, Xm" uniqKey="Wu X">XM Wu</name>
</author>
<author><name sortKey="Ye, Jl" uniqKey="Ye J">JL Ye</name>
</author>
<author><name sortKey="Yu, Kq" uniqKey="Yu K">KQ Yu</name>
</author>
<author><name sortKey="Guo, Ww" uniqKey="Guo W">WW Guo</name>
</author>
<author><name sortKey="Deng, Xx" uniqKey="Deng X">XX Deng</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Xu, Q" uniqKey="Xu Q">Q Xu</name>
</author>
<author><name sortKey="Chen, Ll" uniqKey="Chen L">LL Chen</name>
</author>
<author><name sortKey="Ruan, Xa" uniqKey="Ruan X">XA Ruan</name>
</author>
<author><name sortKey="Chen, Dj" uniqKey="Chen D">DJ Chen</name>
</author>
<author><name sortKey="Zhu, Ad" uniqKey="Zhu A">AD Zhu</name>
</author>
<author><name sortKey="Chen, Cl" uniqKey="Chen C">CL Chen</name>
</author>
<author><name sortKey="Bertrand, D" uniqKey="Bertrand D">D Bertrand</name>
</author>
<author><name sortKey="Jiao, Wb" uniqKey="Jiao W">WB Jiao</name>
</author>
<author><name sortKey="Hao, Bh" uniqKey="Hao B">BH Hao</name>
</author>
<author><name sortKey="Lyon, Mp" uniqKey="Lyon M">MP Lyon</name>
</author>
<author><name sortKey="Chen, J" uniqKey="Chen J">J Chen</name>
</author>
<author><name sortKey="Gao, S" uniqKey="Gao S">S Gao</name>
</author>
<author><name sortKey="Xing, F" uniqKey="Xing F">F Xing</name>
</author>
<author><name sortKey="Lan, H" uniqKey="Lan H">H Lan</name>
</author>
<author><name sortKey="Chang, Jw" uniqKey="Chang J">JW Chang</name>
</author>
<author><name sortKey="Ge, X" uniqKey="Ge X">X Ge</name>
</author>
<author><name sortKey="Lei, Y" uniqKey="Lei Y">Y Lei</name>
</author>
<author><name sortKey="Hu, Q" uniqKey="Hu Q">Q Hu</name>
</author>
<author><name sortKey="Miao, Y" uniqKey="Miao Y">Y Miao</name>
</author>
<author><name sortKey="Wang, L" uniqKey="Wang L">L Wang</name>
</author>
<author><name sortKey="Xiao, S" uniqKey="Xiao S">S Xiao</name>
</author>
<author><name sortKey="Biswas, Mk" uniqKey="Biswas M">MK Biswas</name>
</author>
<author><name sortKey="Zeng, W" uniqKey="Zeng W">W Zeng</name>
</author>
<author><name sortKey="Guo, F" uniqKey="Guo F">F Guo</name>
</author>
<author><name sortKey="Cao, H" uniqKey="Cao H">H Cao</name>
</author>
<author><name sortKey="Yang, X" uniqKey="Yang X">X Yang</name>
</author>
<author><name sortKey="Xu, Xw" uniqKey="Xu X">XW Xu</name>
</author>
<author><name sortKey="Cheng, Yj" uniqKey="Cheng Y">YJ Cheng</name>
</author>
<author><name sortKey="Xu, J" uniqKey="Xu J">J Xu</name>
</author>
<author><name sortKey="Liu, Jh" uniqKey="Liu J">JH Liu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Rajagopalan, R" uniqKey="Rajagopalan R">R Rajagopalan</name>
</author>
<author><name sortKey="Vaucheret, H" uniqKey="Vaucheret H">H Vaucheret</name>
</author>
<author><name sortKey="Trejo, J" uniqKey="Trejo J">J Trejo</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Moxon, S" uniqKey="Moxon S">S Moxon</name>
</author>
<author><name sortKey="Jing, Rc" uniqKey="Jing R">RC Jing</name>
</author>
<author><name sortKey="Szittya, G" uniqKey="Szittya G">G Szittya</name>
</author>
<author><name sortKey="Schwach, F" uniqKey="Schwach F">F Schwach</name>
</author>
<author><name sortKey="Pilcher, Rlr" uniqKey="Pilcher R">RLR Pilcher</name>
</author>
<author><name sortKey="Moulton, V" uniqKey="Moulton V">V Moulton</name>
</author>
<author><name sortKey="Dalmay, T" uniqKey="Dalmay T">T Dalmay</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Addo Quaye, C" uniqKey="Addo Quaye C">C Addo-Quaye</name>
</author>
<author><name sortKey="Eshoo, Tw" uniqKey="Eshoo T">TW Eshoo</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
<author><name sortKey="Axtell, Mj" uniqKey="Axtell M">MJ Axtell</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Vaucheret, H" uniqKey="Vaucheret H">H Vaucheret</name>
</author>
<author><name sortKey="Vazquez, F" uniqKey="Vazquez F">F Vazquez</name>
</author>
<author><name sortKey="Crete, P" uniqKey="Crete P">P Crete</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Vaucheret, H" uniqKey="Vaucheret H">H Vaucheret</name>
</author>
<author><name sortKey="Mallory, Ac" uniqKey="Mallory A">AC Mallory</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Allen, Rs" uniqKey="Allen R">RS Allen</name>
</author>
<author><name sortKey="Li, J" uniqKey="Li J">J Li</name>
</author>
<author><name sortKey="Stahle, Mi" uniqKey="Stahle M">MI Stahle</name>
</author>
<author><name sortKey="Dubroue, A" uniqKey="Dubroue A">A Dubroue</name>
</author>
<author><name sortKey="Gubler, F" uniqKey="Gubler F">F Gubler</name>
</author>
<author><name sortKey="Millar, Aa" uniqKey="Millar A">AA Millar</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Reyes, Jl" uniqKey="Reyes J">JL Reyes</name>
</author>
<author><name sortKey="Chua, Nh" uniqKey="Chua N">NH Chua</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Jeong, Dh" uniqKey="Jeong D">DH Jeong</name>
</author>
<author><name sortKey="Park, S" uniqKey="Park S">S Park</name>
</author>
<author><name sortKey="Zhai, J" uniqKey="Zhai J">J Zhai</name>
</author>
<author><name sortKey="Gurazada, Sg" uniqKey="Gurazada S">SG Gurazada</name>
</author>
<author><name sortKey="De Paoli, E" uniqKey="De Paoli E">E De Paoli</name>
</author>
<author><name sortKey="Meyers, Bc" uniqKey="Meyers B">BC Meyers</name>
</author>
<author><name sortKey="Green, Pj" uniqKey="Green P">PJ Green</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Allen, E" uniqKey="Allen E">E Allen</name>
</author>
<author><name sortKey="Xie, Z" uniqKey="Xie Z">Z Xie</name>
</author>
<author><name sortKey="Gustafson, Am" uniqKey="Gustafson A">AM Gustafson</name>
</author>
<author><name sortKey="Carrington, Jc" uniqKey="Carrington J">JC Carrington</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Xia, R" uniqKey="Xia R">R Xia</name>
</author>
<author><name sortKey="Zhu, H" uniqKey="Zhu H">H Zhu</name>
</author>
<author><name sortKey="An, Y" uniqKey="An Y">Y An</name>
</author>
<author><name sortKey="Beers, Ep" uniqKey="Beers E">EP Beers</name>
</author>
<author><name sortKey="Liu, Z" uniqKey="Liu Z">Z Liu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Tang, S" uniqKey="Tang S">S Tang</name>
</author>
<author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author><name sortKey="Li, Z" uniqKey="Li Z">Z Li</name>
</author>
<author><name sortKey="Gui, Y" uniqKey="Gui Y">Y Gui</name>
</author>
<author><name sortKey="Xiao, B" uniqKey="Xiao B">B Xiao</name>
</author>
<author><name sortKey="Xie, J" uniqKey="Xie J">J Xie</name>
</author>
<author><name sortKey="Zhu, Qh" uniqKey="Zhu Q">QH Zhu</name>
</author>
<author><name sortKey="Fan, L" uniqKey="Fan L">L Fan</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Li, F" uniqKey="Li F">F Li</name>
</author>
<author><name sortKey="Pignatta, D" uniqKey="Pignatta D">D Pignatta</name>
</author>
<author><name sortKey="Bendix, C" uniqKey="Bendix C">C Bendix</name>
</author>
<author><name sortKey="Brunkard, Jo" uniqKey="Brunkard J">JO Brunkard</name>
</author>
<author><name sortKey="Cohn, Mm" uniqKey="Cohn M">MM Cohn</name>
</author>
<author><name sortKey="Tung, J" uniqKey="Tung J">J Tung</name>
</author>
<author><name sortKey="Sun, H" uniqKey="Sun H">H Sun</name>
</author>
<author><name sortKey="Kumar, P" uniqKey="Kumar P">P Kumar</name>
</author>
<author><name sortKey="Baker, B" uniqKey="Baker B">B Baker</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Chen, M" uniqKey="Chen M">M Chen</name>
</author>
<author><name sortKey="Tan, Zy" uniqKey="Tan Z">ZY Tan</name>
</author>
<author><name sortKey="Zeng, Gm" uniqKey="Zeng G">GM Zeng</name>
</author>
<author><name sortKey="Peng, J" uniqKey="Peng J">J Peng</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Li, Yc" uniqKey="Li Y">YC Li</name>
</author>
<author><name sortKey="Korol, Ab" uniqKey="Korol A">AB Korol</name>
</author>
<author><name sortKey="Fahima, T" uniqKey="Fahima T">T Fahima</name>
</author>
<author><name sortKey="Beiles, A" uniqKey="Beiles A">A Beiles</name>
</author>
<author><name sortKey="Nevo, E" uniqKey="Nevo E">E Nevo</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Zhang, L" uniqKey="Zhang L">L Zhang</name>
</author>
<author><name sortKey="Chia, J M" uniqKey="Chia J">J-M Chia</name>
</author>
<author><name sortKey="Kumari, S" uniqKey="Kumari S">S Kumari</name>
</author>
<author><name sortKey="Stein, Jc" uniqKey="Stein J">JC Stein</name>
</author>
<author><name sortKey="Liu, Z" uniqKey="Liu Z">Z Liu</name>
</author>
<author><name sortKey="Narechania, A" uniqKey="Narechania A">A Narechania</name>
</author>
<author><name sortKey="Maher, Ca" uniqKey="Maher C">CA Maher</name>
</author>
<author><name sortKey="Guill, K" uniqKey="Guill K">K Guill</name>
</author>
<author><name sortKey="Mcmullen, Md" uniqKey="Mcmullen M">MD McMullen</name>
</author>
<author><name sortKey="Ware, D" uniqKey="Ware D">D Ware</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Pantaleo, V" uniqKey="Pantaleo V">V Pantaleo</name>
</author>
<author><name sortKey="Szittya, G" uniqKey="Szittya G">G Szittya</name>
</author>
<author><name sortKey="Moxon, S" uniqKey="Moxon S">S Moxon</name>
</author>
<author><name sortKey="Miozzi, L" uniqKey="Miozzi L">L Miozzi</name>
</author>
<author><name sortKey="Moulton, V" uniqKey="Moulton V">V Moulton</name>
</author>
<author><name sortKey="Dalmay, T" uniqKey="Dalmay T">T Dalmay</name>
</author>
<author><name sortKey="Burgyan, J" uniqKey="Burgyan J">J Burgyan</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Takada, S" uniqKey="Takada S">S Takada</name>
</author>
<author><name sortKey="Hibara, K I" uniqKey="Hibara K">K-i Hibara</name>
</author>
<author><name sortKey="Ishida, T" uniqKey="Ishida T">T Ishida</name>
</author>
<author><name sortKey="Tasaka, M" uniqKey="Tasaka M">M Tasaka</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Mallory, Ac" uniqKey="Mallory A">AC Mallory</name>
</author>
<author><name sortKey="Dugas, Dv" uniqKey="Dugas D">DV Dugas</name>
</author>
<author><name sortKey="Bartel, Dp" uniqKey="Bartel D">DP Bartel</name>
</author>
<author><name sortKey="Bartel, B" uniqKey="Bartel B">B Bartel</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Guo, Y" uniqKey="Guo Y">Y Guo</name>
</author>
<author><name sortKey="Gan, S" uniqKey="Gan S">S Gan</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Nakashima, K" uniqKey="Nakashima K">K Nakashima</name>
</author>
<author><name sortKey="Tran, Lsp" uniqKey="Tran L">LSP Tran</name>
</author>
<author><name sortKey="Van Nguyen, D" uniqKey="Van Nguyen D">D Van Nguyen</name>
</author>
<author><name sortKey="Fujita, M" uniqKey="Fujita M">M Fujita</name>
</author>
<author><name sortKey="Maruyama, K" uniqKey="Maruyama K">K Maruyama</name>
</author>
<author><name sortKey="Todaka, D" uniqKey="Todaka D">D Todaka</name>
</author>
<author><name sortKey="Ito, Y" uniqKey="Ito Y">Y Ito</name>
</author>
<author><name sortKey="Hayashi, N" uniqKey="Hayashi N">N Hayashi</name>
</author>
<author><name sortKey="Shinozaki, K" uniqKey="Shinozaki K">K Shinozaki</name>
</author>
<author><name sortKey="Yamaguchi Shinozaki, K" uniqKey="Yamaguchi Shinozaki K">K Yamaguchi-Shinozaki</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Shan, W" uniqKey="Shan W">W Shan</name>
</author>
<author><name sortKey="Kuang, J F" uniqKey="Kuang J">J-f Kuang</name>
</author>
<author><name sortKey="Chen, L" uniqKey="Chen L">L Chen</name>
</author>
<author><name sortKey="Xie, H" uniqKey="Xie H">H Xie</name>
</author>
<author><name sortKey="Peng, H H" uniqKey="Peng H">H-h Peng</name>
</author>
<author><name sortKey="Xiao, Y Y" uniqKey="Xiao Y">Y-y Xiao</name>
</author>
<author><name sortKey="Li, X P" uniqKey="Li X">X-p Li</name>
</author>
<author><name sortKey="Chen, W X" uniqKey="Chen W">W-x Chen</name>
</author>
<author><name sortKey="He, Q G" uniqKey="He Q">Q-g He</name>
</author>
<author><name sortKey="Chen, J Y" uniqKey="Chen J">J-y Chen</name>
</author>
<author><name sortKey="Lu, W J" uniqKey="Lu W">W-j Lu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Fan, J" uniqKey="Fan J">J Fan</name>
</author>
<author><name sortKey="Gao, X" uniqKey="Gao X">X Gao</name>
</author>
<author><name sortKey="Yang, Y W" uniqKey="Yang Y">Y-W Yang</name>
</author>
<author><name sortKey="Deng, W" uniqKey="Deng W">W Deng</name>
</author>
<author><name sortKey="Li, Z G" uniqKey="Li Z">Z-G Li</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Liu, Y Z" uniqKey="Liu Y">Y-Z Liu</name>
</author>
<author><name sortKey="Baig, M" uniqKey="Baig M">M Baig</name>
</author>
<author><name sortKey="Fan, R" uniqKey="Fan R">R Fan</name>
</author>
<author><name sortKey="Ye, J L" uniqKey="Ye J">J-L Ye</name>
</author>
<author><name sortKey="Cao, Y C" uniqKey="Cao Y">Y-C Cao</name>
</author>
<author><name sortKey="Deng, X X" uniqKey="Deng X">X-X Deng</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Chen, Cf" uniqKey="Chen C">CF Chen</name>
</author>
<author><name sortKey="Ridzon, Da" uniqKey="Ridzon D">DA Ridzon</name>
</author>
<author><name sortKey="Broomer, Aj" uniqKey="Broomer A">AJ Broomer</name>
</author>
<author><name sortKey="Zhou, Zh" uniqKey="Zhou Z">ZH Zhou</name>
</author>
<author><name sortKey="Lee, Dh" uniqKey="Lee D">DH Lee</name>
</author>
<author><name sortKey="Nguyen, Jt" uniqKey="Nguyen J">JT Nguyen</name>
</author>
<author><name sortKey="Barbisin, M" uniqKey="Barbisin M">M Barbisin</name>
</author>
<author><name sortKey="Xu, Nl" uniqKey="Xu N">NL Xu</name>
</author>
<author><name sortKey="Mahuvakar, Vr" uniqKey="Mahuvakar V">VR Mahuvakar</name>
</author>
<author><name sortKey="Andersen, Mr" uniqKey="Andersen M">MR Andersen</name>
</author>
<author><name sortKey="Lao, Kq" uniqKey="Lao K">KQ Lao</name>
</author>
<author><name sortKey="Livak, Kj" uniqKey="Livak K">KJ Livak</name>
</author>
<author><name sortKey="Guegler, Kj" uniqKey="Guegler K">KJ Guegler</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Varkonyi Gasic, E" uniqKey="Varkonyi Gasic E">E Varkonyi-Gasic</name>
</author>
<author><name sortKey="Wu, Rm" uniqKey="Wu R">RM Wu</name>
</author>
<author><name sortKey="Wood, M" uniqKey="Wood M">M Wood</name>
</author>
<author><name sortKey="Walton, Ef" uniqKey="Walton E">EF Walton</name>
</author>
<author><name sortKey="Hellens, Rp" uniqKey="Hellens R">RP Hellens</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Kou, Sj" uniqKey="Kou S">SJ Kou</name>
</author>
<author><name sortKey="Wu, Xm" uniqKey="Wu X">XM Wu</name>
</author>
<author><name sortKey="Liu, Z" uniqKey="Liu Z">Z Liu</name>
</author>
<author><name sortKey="Liu, Yl" uniqKey="Liu Y">YL Liu</name>
</author>
<author><name sortKey="Xu, Q" uniqKey="Xu Q">Q Xu</name>
</author>
<author><name sortKey="Guo, Ww" uniqKey="Guo W">WW Guo</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Sparkes, Ia" uniqKey="Sparkes I">IA Sparkes</name>
</author>
<author><name sortKey="Runions, J" uniqKey="Runions J">J Runions</name>
</author>
<author><name sortKey="Kearns, A" uniqKey="Kearns A">A Kearns</name>
</author>
<author><name sortKey="Hawes, C" uniqKey="Hawes C">C Hawes</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMC Genomics</journal-id>
<journal-id journal-id-type="iso-abbrev">BMC Genomics</journal-id>
<journal-title-group><journal-title>BMC Genomics</journal-title>
</journal-title-group>
<issn pub-type="epub">1471-2164</issn>
<publisher><publisher-name>BioMed Central</publisher-name>
<publisher-loc>London</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25142253</article-id>
<article-id pub-id-type="pmc">4158063</article-id>
<article-id pub-id-type="publisher-id">6413</article-id>
<article-id pub-id-type="doi">10.1186/1471-2164-15-695</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Genome-wide comparison of microRNAs and their targeted transcripts among leaf, flower and fruit of sweet orange</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Liu</surname>
<given-names>Yuanlong</given-names>
</name>
<address><email>whitepig1989@163.com</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wang</surname>
<given-names>Lun</given-names>
</name>
<address><email>wanglun@webmail.hzau.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Chen</surname>
<given-names>Dijun</given-names>
</name>
<address><email>chendijun@zju.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff2"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wu</surname>
<given-names>Xiaomeng</given-names>
</name>
<address><email>ema@webmail.hzau.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Huang</surname>
<given-names>Ding</given-names>
</name>
<address><email>hdh016@126.com</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Chen</surname>
<given-names>Lingling</given-names>
</name>
<address><email>llchen@mail.hzau.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff2"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Li</surname>
<given-names>Li</given-names>
</name>
<address><email>ll37@cornell.edu</email>
</address>
<xref ref-type="aff" rid="Aff3"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Deng</surname>
<given-names>Xiuxin</given-names>
</name>
<address><email>xxdeng@mail.hzau.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author" corresp="yes"><name><surname>Xu</surname>
<given-names>Qiang</given-names>
</name>
<address><email>xuqiang@mail.hzau.edu.cn</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<aff id="Aff1"><label></label>
Key Laboratory of Horticultural Plant Biology of Ministry of Education, Huazhong Agricultural University, Wuhan, 430070 China</aff>
<aff id="Aff2"><label></label>
Center for Bioinformatics, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, 430070 China</aff>
<aff id="Aff3"><label></label>
Robert W. Holley Center for Agriculture and Health, Cornell University, Ithaca, NY 14853 USA</aff>
</contrib-group>
<pub-date pub-type="epub"><day>20</day>
<month>8</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>20</day>
<month>8</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="collection"><year>2014</year>
</pub-date>
<volume>15</volume>
<issue>1</issue>
<elocation-id>695</elocation-id>
<history><date date-type="received"><day>4</day>
<month>6</month>
<year>2014</year>
</date>
<date date-type="accepted"><day>15</day>
<month>8</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>© Liu et al.; licensee BioMed Central Ltd. 2014</copyright-statement>
<license license-type="open-access"><license-p>This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0">http://creativecommons.org/licenses/by/4.0</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>
) applies to the data made available in this article, unless otherwise stated.</license-p>
</license>
</permissions>
<abstract id="Abs1"><sec><title>Background</title>
<p>In plants, microRNAs (miRNAs) regulate gene expression mainly at the post-transcriptional level. Previous studies have demonstrated that miRNA-mediated gene silencing pathways play vital roles in plant development. Here, we used a high-throughput sequencing approach to characterize the miRNAs and their targeted transcripts in the leaf, flower and fruit of sweet orange.</p>
</sec>
<sec><title>Results</title>
<p>A total of 183 known miRNAs and 38 novel miRNAs were identified. An in-house script was used to identify all potential secondary siRNAs derived from miRNA-targeted transcripts using sRNA and degradome sequencing data. Genome mapping revealed that these miRNAs were evenly distributed across the genome with several small clusters, and 69 pre-miRNAs were co-localized with simple sequence repeats (SSRs). Noticeably, the loop size of pre-miR396c was influenced by the repeat number of CUU unit. The expression pattern of miRNAs among different tissues and developmental stages were further investigated by both qRT-PCR and RNA gel blotting. Interestingly, Csi-miR164 was highly expressed in fruit ripening stage, and was validated to target a NAC transcription factor. This study depicts a global picture of miRNAs and their target genes in the genome of sweet orange, and focused on the comparison among leaf, flower and fruit tissues.</p>
</sec>
<sec><title>Conclusions</title>
<p>This study provides a global view of miRNAs and their target genes in different tissue of sweet orange, and focused on the identification of miRNA involved in the regulation of fruit ripening. The results of this study lay a foundation for unraveling key regulators of orange fruit development and ripening on post-transcriptional level.</p>
</sec>
<sec><title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/1471-2164-15-695) contains supplementary material, which is available to authorized users.</p>
</sec>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd><italic>Citrus sinensis</italic>
</kwd>
<kwd>miRNA</kwd>
<kwd>Degraded transcript</kwd>
<kwd>Genome-wide comparison</kwd>
<kwd>Fruit ripening</kwd>
</kwd-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© The Author(s) 2014</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body><sec id="Sec1"><title>Background</title>
<p>Micro RNAs (miRNAs), which are typically 20–24 nucleotides (nt) in length, are derived from primary miRNA transcripts (pri-miRNAs) that contain a stem-loop secondary structure. The pri-miRNA is processed in the nucleus by DCL1, a Dicer-like protein, to create a miRNA-miRNA* duplex, where miRNA* is a passenger strand complementary to the miRNA. The duplex is then separated by helicase and the mature miRNA is incorporated into an ARGONAUTE 1 (AGO1) protein to form an RNA-induced silencing complex (RISC) [<xref ref-type="bibr" rid="CR1">1</xref>
, <xref ref-type="bibr" rid="CR2">2</xref>
]. Target genes that contain a sequence with almost complete complementary to the miRNA are cleaved by the RISC at a specific site opposite to the 10th or 11th nucleotide in the miRNA. The miRNA* species is thought to be degraded [<xref ref-type="bibr" rid="CR1">1</xref>
, <xref ref-type="bibr" rid="CR3">3</xref>
]. However, recent research demonstrated that AGO-associated miRNA393* guides the silencing of a golgi-localized SNARE gene, indicating that miRNA* species may be capable of functioning as miRNAs [<xref ref-type="bibr" rid="CR4">4</xref>
].</p>
<p>Typically, miRNA-guided cleavage represses target gene expression; however, a group of 22 nt miRNAs also trigger secondary siRNA biogenesis in plants [<xref ref-type="bibr" rid="CR5">5</xref>
]. Some 22 nt miRNAs are generated from bulged duplexes comprising a 22 nt miRNA and a 21 nt miRNA*; these duplexes are processed by DCL1. By contrast, DCL2 generates 22 nt miRNAs by processing perfect duplexes comprising a 22 nt miRNA and a 22 nt miRNA*. The latter type of 22 nt miRNA may trigger secondary siRNA biogenesis. During this process, the miRNA is incorporated into AGO1 which guides 5’ cleavage of the target, and then RNA-dependent RNA polymerase 6 (RDR6) synthesizes a double-stranded RNA fragment that is subsequently cut into secondary siRNAs. With the exception of the 24 nt secondary siRNAs (triggered by miR2775), most secondary siRNAs are 21 nt in length [<xref ref-type="bibr" rid="CR5">5</xref>
, <xref ref-type="bibr" rid="CR6">6</xref>
]. The mechanism of biogenesis of trans-acting siRNAs (tasiRNAs) generated from <italic>TAS3</italic>
differs from that described above. A complex comprising miR390 and AGO7 binds to <italic>TAS3</italic>
at two sites and guides the cleavage of the tasiRNA precursor. The cleavage product is then converted to double-stranded RNA by RDR6 and DCL4, and tasiRNAs are generated one by one from the cleavage site to the 5’ side. All of the secondary siRNAs described above may incorporate into AGOs and function similarly as miRNAs [<xref ref-type="bibr" rid="CR6">6</xref>
, <xref ref-type="bibr" rid="CR7">7</xref>
].</p>
<p>Traditional cloning and sequencing methods have been used to identify miRNAs in model plants, including <italic>Arabidopsis</italic>
, rice and poplar. Comparison of the sequences of miRNAs from these species has revealed that most are highly conserved [<xref ref-type="bibr" rid="CR8">8</xref>
]. Nevertheless, a number of non-conserved miRNAs may be family-specific or species-specific. Generally, non-conserved miRNAs are expressed at a lower level than conserved miRNAs. Recently, high-throughput sequencing has been used for the identification and expression profiling of miRNAs in many horticultural plants, including tomato, grape, papaya, radish and trifoliate orange [<xref ref-type="bibr" rid="CR9">9</xref>
–<xref ref-type="bibr" rid="CR13">13</xref>
]. Accurate identification of miRNAs from large amounts of sequencing data is challenging; therefore, minimal criteria for annotation of miRNAs in plants were consolidated [<xref ref-type="bibr" rid="CR14">14</xref>
]. A miRNA-mediated degraded fragments sequencing (degradome sequencing) approach was also reported to be capable of efficient characterization of miRNA target genes [<xref ref-type="bibr" rid="CR15">15</xref>
]. This method involves ligation of the 3’ fragment generated by RISC, which contains a 5’-monophosphate, to a 5’ RACE adaptor. Reverse transcription is then performed using oligo(dT) as a 3’ adaptor and the cDNAs formed by second strand synthesis are digested with <italic>MmeI</italic>
to generate 20 bp signatures that are sequenced and used to identify miRNA target pairs [<xref ref-type="bibr" rid="CR15">15</xref>
–<xref ref-type="bibr" rid="CR17">17</xref>
].</p>
<p>As described above, miRNAs act as regulators of plant development [<xref ref-type="bibr" rid="CR18">18</xref>
, <xref ref-type="bibr" rid="CR19">19</xref>
]; miR156, miR164 and miR166, in particular, play important roles in regulating leaf development [<xref ref-type="bibr" rid="CR20">20</xref>
–<xref ref-type="bibr" rid="CR24">24</xref>
]. Additionally, miR156, miR159, miR319 and miR172 are involved in flowering regulation and phase changing from vegetative growth to reproductive growth [<xref ref-type="bibr" rid="CR21">21</xref>
, <xref ref-type="bibr" rid="CR25">25</xref>
–<xref ref-type="bibr" rid="CR29">29</xref>
]. Overexpression of osmiR397 leads to increasing rice size and promoting panicle branching [<xref ref-type="bibr" rid="CR30">30</xref>
]. The understanding of the roles of miRNA in the regulation of reproductive growth is further improved by recent research on non-conserved (novel) miRNAs; for example, miR4376 in the Solanaceae regulates a Ca<sup>2+</sup>
-ATPase involved in tomato reproductive growth [<xref ref-type="bibr" rid="CR31">31</xref>
].</p>
<p>The first report of miRNAs in the Rutaceae family was in <italic>Poncirus trifoliata</italic>
[<xref ref-type="bibr" rid="CR32">32</xref>
] and high-throughput sequencing was recently used to identify miRNAs and their targets in this species [<xref ref-type="bibr" rid="CR33">33</xref>
, <xref ref-type="bibr" rid="CR34">34</xref>
]. Our group previously identified miRNAs in sweet orange (<italic>Citrus sinensis</italic>
) by using EST assembly as reference to dig out miRNA seqeunces [<xref ref-type="bibr" rid="CR35">35</xref>
]. Here, based on our recently published sweet orange genome [<xref ref-type="bibr" rid="CR36">36</xref>
], we performed a genome-wide characterization of sRNAs (the sRNAome) and their targets (the degradome) in the leaves, flowers and fruits of sweet orange (<italic>C. sinensis</italic>
[L.] Osbeck). A total of 183 known and 38 novel miRNAs were identified; the tissue specifically expressed miRNAs were validated with the aim of identifying miRNAs involved in the regulation of fruit development and maturation.</p>
</sec>
<sec id="Sec2"><title>Results and discussion</title>
<sec id="Sec3"><title>Sequencing of sRNAs and the degradome</title>
<p>The Illumina sequencing data of sRNAs from leaf, flower and fruit showed that 24 nt sRNAs are the most abundant and very few longer sRNAs (Figure <xref rid="Fig1" ref-type="fig">1</xref>
). The greater abundance of 24 nt sRNAs rather than 21 nt sRNAs in all three tissues agrees with the results observed for other dicots [<xref ref-type="bibr" rid="CR37">37</xref>
, <xref ref-type="bibr" rid="CR38">38</xref>
]. After discarding low quality reads and sequence counts lower than 3 in each library, clean reads were produced. The clean reads were then compared with the sequence of the <italic>C. sinensis</italic>
genome [<xref ref-type="bibr" rid="CR36">36</xref>
]. Overall, perfect matches with the <italic>C. sinensis</italic>
genome were obtained for 61.21%, 58.56% and 76.30% of unique sRNAs from leaf, flower and fruit, respectively (Table <xref rid="Tab1" ref-type="table">1</xref>
). The sRNA tags were annotated with sequences from the Rfam database to eliminate non-coding RNAs, including rRNA, tRNA, snRNA and snoRNA. A search of the miRBase database (v16) identified 2699, 1985 and 771 unique matches for the sRNAs identified in leaf, flower and fruit, respectively (Table <xref rid="Tab1" ref-type="table">1</xref>
). A BLAST search of miRBase identified 183 known miRNAs based on sequence similarity and the presence of a stem-loop structure in the precursor. The sRNA clean reads that were not known miRNAs were mapped to the genome and were used to predict novel miRNAs according to the structure and expression criteria [<xref ref-type="bibr" rid="CR14">14</xref>
]. Finally, 38 candidate novel miRNAs with a clear precursor containing a stem-loop secondary structure were identified (Additional files <xref rid="MOESM1" ref-type="media">1</xref>
and <xref rid="MOESM2" ref-type="media">2</xref>
).<fig id="Fig1"><label>Figure 1</label>
<caption><p><bold>Lengths of the sweet orange sRNAs identified in leaf, flower and fruit tissues.</bold>
The sRNAome sequencing data are expressed as a percentage of the total number of the unique sRNAs identified in each sample type.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig1_HTML" id="d30e554"></graphic>
</fig>
</p>
<table-wrap id="Tab1"><label>Table 1</label>
<caption><p><bold>Characteristics of the sRNAs identified in orange leaf, flower and fruit</bold>
</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th></th>
<th></th>
<th>Total sRNAs</th>
<th>Unique sRNAs</th>
</tr>
</thead>
<tbody><tr><td>Leaf</td>
<td>Raw reads</td>
<td>18961890</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>10174438 (100%)</td>
<td>586073 (100%)</td>
</tr>
<tr><td></td>
<td>Match genome</td>
<td>6234563 (61.28%)</td>
<td>358731 (61.21%)</td>
</tr>
<tr><td></td>
<td>Match miRbase<sup>b</sup>
</td>
<td>1068582 (10.50%)</td>
<td>2699 (0.46%)</td>
</tr>
<tr><td>Flower</td>
<td>Raw reads</td>
<td>17841995</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>9252302 (100%)</td>
<td>612511 (100%)</td>
</tr>
<tr><td></td>
<td>Match genome</td>
<td>5172633 (55.91%)</td>
<td>358709 (58.56%)</td>
</tr>
<tr><td></td>
<td>Match miRbase<sup>b</sup>
</td>
<td>559470 (6.05%)</td>
<td>1985 (0.32%)</td>
</tr>
<tr><td>Fruit</td>
<td>Raw reads<sup>c</sup>
</td>
<td>4598696</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>1785395 (100%)</td>
<td>202965 (100%)</td>
</tr>
<tr><td></td>
<td>Match genome</td>
<td>1415319 (79.27%)</td>
<td>154864 (76.30%)</td>
</tr>
<tr><td></td>
<td>Match miRbase<sup>b</sup>
</td>
<td>55653 (3.12%)</td>
<td>771 (0.38%)</td>
</tr>
</tbody>
</table>
<table-wrap-foot><p><sup>a</sup>
Low quality sequences containing ambiguous nucleotides, sequences shorter than 18 nt, and sequence counts lower than three were removed.</p>
<p><sup>b</sup>
Small RNAs matching miRbase (v16) with a maximum of two mismatches (if gap exist, number of gaps plus mismatches ≤ 5).</p>
<p><sup>c</sup>
The raw reads of fruit sRNA library were from our previous research (Xu et al. [<xref ref-type="bibr" rid="CR35">35</xref>
]).</p>
</table-wrap-foot>
</table-wrap>
<p>To identify the target genes of miRNAs, a high-throughput experimental approach was used to sequence the degradome libraries of the leaf, flower and fruit tissues. After discarding low quality sequences, more than 17 million clean reads were obtained for each tissue. The cDNA sequences annotated from orange genome platform [<xref ref-type="bibr" rid="CR36">36</xref>
] was used as the mRNA reference dataset and the combination of 183 known miRNAs and 38 novel miRNAs was used as the miRNA reference dataset. Overall, perfect matches with the mRNA reference dataset were obtained for 72.86%, 67.12% and 56.42% of unique tags from the leaf, flower and fruit samples, respectively (Table <xref rid="Tab2" ref-type="table">2</xref>
). In addition, 55257, 62365 and 19393 degraded mRNA fragments of miRNA targets were identified in leaf, flower and fruit, respectively. The miRNA reference dataset and the degraded fragments were then used to generate miRNA-mRNA pairs. A total of 405 targets were identified for 107 miRNAs which expressed in leaf. In addition, 265 targets were identified for 166 miRNAs in flower and 322 targets were identified for 118 miRNAs in fruit (Additional file <xref rid="MOESM3" ref-type="media">3</xref>
). Confidence evaluation of degradome data was performed as reported previously [<xref ref-type="bibr" rid="CR16">16</xref>
, <xref ref-type="bibr" rid="CR39">39</xref>
]. The target transcripts were divided into three classes (category I, category II and category III; Additional file <xref rid="MOESM4" ref-type="media">4</xref>
). In category I, the miRNA-guided cleavage fragment was the most abundant tag matching the transcript; therefore, category I is most reliable for the detection of miRNA-targeted genes. In category II, the miRNA-guided cleavage fragment was not the most abundant fragment; however, it still formed a clear peak in the T-plot. The remaining target transcripts were classified into category III (Additional file <xref rid="MOESM4" ref-type="media">4</xref>
).<table-wrap id="Tab2"><label>Table 2</label>
<caption><p><bold>Characteristics of the degradome sequences from orange leaf, flower and fruit</bold>
</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th></th>
<th></th>
<th>Total RNAs</th>
<th>Unique RNAs</th>
</tr>
</thead>
<tbody><tr><td>Leaf</td>
<td>Raw reads</td>
<td>22826037</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>20566571 (100%)</td>
<td>1448803 (100%)</td>
</tr>
<tr><td></td>
<td>Match mRNA reference dataset</td>
<td>17683257 (85.98%)</td>
<td>1055651 (72.86%)</td>
</tr>
<tr><td>Flower</td>
<td>Raw reads</td>
<td>19030542</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>17629275 (100%)</td>
<td>1093131 (100%)</td>
</tr>
<tr><td></td>
<td>Match mRNA reference dataset</td>
<td>14577696 (82.69%)</td>
<td>733751 (67.12%)</td>
</tr>
<tr><td>Fruit</td>
<td>Raw reads</td>
<td>21213198</td>
<td></td>
</tr>
<tr><td></td>
<td>Clean reads<sup>a</sup>
</td>
<td>18284467 (100%)</td>
<td>331940 (100%)</td>
</tr>
<tr><td></td>
<td>Match mRNA reference dataset</td>
<td>16047135 (87.76%)</td>
<td>187295 (56.42%)</td>
</tr>
</tbody>
</table>
<table-wrap-foot><p><sup>a</sup>
Low quality sequences, sequences shorter than 18 nt, and adaptor contaminants were removed.</p>
</table-wrap-foot>
</table-wrap>
</p>
</sec>
<sec id="Sec4"><title>Known miRNAs and their targets in the leaf, flower and fruit tissues</title>
<p>A total of 183 known miRNAs, including 53 isoforms with high expression level, belonging to 58 families, were identified. The sweet orange genome sequence was used to predict RNA secondary structures; all of the precursors of the 183 known miRNAs had regular stem-loop secondary structures (Additional file <xref rid="MOESM1" ref-type="media">1</xref>
).</p>
<p>Comparison of the normalized expression levels of miRNAs in the leaf, flower and fruit tissues revealed that 60 known miRNAs displayed higher expression (>2 fold change) in leaf than those in flower or fruit; 33 known miRNAs showed higher expression in flower; and 32 known miRNAs displayed higher expression in fruit (Figure <xref rid="Fig2" ref-type="fig">2</xref>
and Additional file <xref rid="MOESM2" ref-type="media">2</xref>
). For example, csi-miR477a-3p, csi-miR827.1 and csi-miR168a showed much higher expression levels (>4 fold change) in fruit. In addition, some miRNAs, including csi-miR166j.1, csi-miR166j.3, csi-miR4414.1, csi-miR391b, csi-miR1432a, the csi-miR169 family and the csi-miR171 family, were expressed in leaf and flower but were not detected in fruit.<fig id="Fig2"><label>Figure 2</label>
<caption><p><bold>Heat map of the normalized expression level (TPM) of all miRNAs.</bold>
miRNAs belong to group 1 are highly expressed in leaf; miRNAs belong to group 2 are highly expressed in flower; miRNAs belong to group 3 are highly expressed in fruit. The colorbar is shown at the bottom of the figure.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig2_HTML" id="d30e945"></graphic>
</fig>
</p>
<p>The targets of known and conserved miRNA families were identified from the degradome data. The target genes were divided into three categories as described above. A total of 395 targets of 100 known miRNAs were identified in leaf degradome data; of these targets, 259 were classified into category I, 38 into category II, and 98, into category III. In flower, 241 targets of 142 known miRNAs were identified; 105, 26 and 110 were classified into categories I, II and III, respectively. In fruit, 301 targets of 101 known miRNAs were identified; of these targets, 107, 66 and 128 were grouped into categories I, II and III, respectively (Additional files <xref rid="MOESM3" ref-type="media">3</xref>
and <xref rid="MOESM4" ref-type="media">4</xref>
;).Most of the conserved miRNAs have similar targets to <italic>Arabidopsis thaliana</italic>
[<xref ref-type="bibr" rid="CR28">28</xref>
]. Multiple targets were also observed for these miRNAs. For example, the miR168 family controls feedback regulation of AGO 1 as previously reported [<xref ref-type="bibr" rid="CR40">40</xref>
, <xref ref-type="bibr" rid="CR41">41</xref>
].</p>
<p>The miRNAs and their targeted transcripts from leaf, flower and fruit tissues indicated that a single miRNA may target genes in a tissue-specific manner. In most circumstance, conserved known miRNAs had the same or homologous targets as other plant species, and most of them were grouped into category I. However, a minority of the conserved miRNAs had different targets in specific tissues. An interesting example was csi-miR168a; the finding that this miRNA targeted AGO1 as a feedback regulator in all three tissues is consistent with previous reports [<xref ref-type="bibr" rid="CR40">40</xref>
, <xref ref-type="bibr" rid="CR41">41</xref>
]. Additionally, csi-miR168a was found to specifically target a CUP-SHAPED COTYLEDON 2 (<italic>CUC2)</italic>
gene in leaves and a pantothenate kinase gene in fruit, as highly supported by the degradome data from different tissues (Additional file <xref rid="MOESM5" ref-type="media">5</xref>
a). Therefore, csi-miR168a is not only involved in stabilizing the accumulation of AGO1, but also has additional roles in the leaf and fruit biology. Another example is that csi-miR159 family was detected to target the transcription factor GAMYB in leaf and flower in consistency with previous reports [<xref ref-type="bibr" rid="CR42">42</xref>
, <xref ref-type="bibr" rid="CR43">43</xref>
]. However, in fruit, degraded fragments of <italic>GAMYB</italic>
generated by csi-miR159 were absent and this miRNA was found to targete <italic>Cs8g05120</italic>
which was annotated as the LRR-containing protein DRT100 with potential roles in DNA damage repair (Additional file <xref rid="MOESM5" ref-type="media">5</xref>
b). A previous study in rice also demonstrated that members from the same miRNA family can have different expression patterns, and this expression difference affects the selectiveness of target gene [<xref ref-type="bibr" rid="CR44">44</xref>
]. These observations indicated that conserved miRNAs may fulfill additional regulatory roles in specific tissue in addition to the conserved and general functions across plant species.</p>
</sec>
<sec id="Sec5"><title>Novel miRNAs and their targets in the leaf, flower and fruit tissues</title>
<p>A total of 38 candidate novel miRNAs with a clear precursor containing a stem-loop secondary structure were identified (Additional file <xref rid="MOESM1" ref-type="media">1</xref>
). The complementary miRNA* sequences for each candidate novel miRNAs were also detected, although most were present at a lower level than their corresponding miRNAs. Unfortunately, we were unable to determine if biogenesis of these candidate novel miRNAs is dependent on DCL1 because of the lack of availability of a <italic>C. sinensis</italic>
DCL1 mutant strain.</p>
<p>More than half of the novel miRNAs identified was expressed at high levels (greater than 10 TPM). 11 novel miRNAs showed higher expression in leaf than flower or fruit; 7 novel miRNAs showed higher expression in flower than leaf or fruit; and 4 novel miRNAs displayed higher expression in fruit than leaf or flower. For example, csi-miRN27 and csi-miRN31 showed higher expression in fruit than leaf or flower (Figure <xref rid="Fig2" ref-type="fig">2</xref>
and Additional file <xref rid="MOESM2" ref-type="media">2</xref>
).</p>
<p>From the degradome data, 10 targets of seven novel miRNAs were identified in leaf; of these targets, 5, 2 and 3 were classified into categories I, II and III, respectively. A total of 24 targets of 24 novel miRNAs in flower were identified; three of these targets were classified into category I, two were grouped into category II, and the remaining 19 were classified into category III. In fruit, 21 targets of 17 miRNAs were identified, of which four were classified into category I, three were grouped into category II, and 14 were classified into category III (Additional file <xref rid="MOESM3" ref-type="media">3</xref>
). In summary, nine target genes of novel miRNAs were grouped into category I, some of which had multiple predicted functions. <italic>Cs8g09620</italic>
, which is annotated as an flowering-related (SRF-type transcription factor family) protein, was identified as a target of csi-miRN7; and <italic>Cs1g12230</italic>
, which is annotated as a light control (FAR1-RELATED SEQUENCE 6 ) protein, was identified as a target of csi-miRN20. Some of the identified targets were not sufficiently annotated; for example, <italic>Cs4g15010</italic>
(category II), targeted by csi-miRN28, was annotated as a putative uncharacterized protein. (Additional files <xref rid="MOESM3" ref-type="media">3</xref>
, <xref rid="MOESM4" ref-type="media">4</xref>
and <xref rid="MOESM6" ref-type="media">6</xref>
and Table <xref rid="Tab3" ref-type="table">3</xref>
).<table-wrap id="Tab3"><label>Table 3</label>
<caption><p><bold>Target genes grouped into category I of novel miRNAs in orange</bold>
</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th></th>
<th></th>
<th colspan="3">Category</th>
<th></th>
</tr>
<tr><th>Novel miRNA</th>
<th>Target gene</th>
<th>in leaves</th>
<th>in flowers</th>
<th>in fruit</th>
<th>Annotation</th>
</tr>
</thead>
<tbody><tr><td>Csi-miRN02</td>
<td>Cs1g08400</td>
<td>I</td>
<td>N/A</td>
<td>N/A</td>
<td>Chaperonin CPN60-1</td>
</tr>
<tr><td>Csi-miRN02</td>
<td>Cs3g18790</td>
<td>I</td>
<td>II</td>
<td>I</td>
<td>Alkylated DNA repair protein alkB homolog 8</td>
</tr>
<tr><td>Csi-miRN02</td>
<td>Cs8g12570</td>
<td>I</td>
<td>N/A</td>
<td>N/A</td>
<td>LRR receptor-like serine/threonine-protein kinase EFR</td>
</tr>
<tr><td>Csi-miRN07</td>
<td>Cs8g09620</td>
<td>III</td>
<td>I</td>
<td>N/A</td>
<td>SRF-type transcription factor family protein</td>
</tr>
<tr><td>Csi-miRN11</td>
<td>Cs8g13560</td>
<td>I</td>
<td>III</td>
<td>I</td>
<td>No annotation</td>
</tr>
<tr><td>Csi-miRN20</td>
<td>Cs1g12230</td>
<td>N/A</td>
<td>N/A</td>
<td>I</td>
<td>Protein FAR1-RELATED SEQUENCE 6</td>
</tr>
<tr><td>Csi-miRN20</td>
<td>Cs3g05320</td>
<td>I</td>
<td>III</td>
<td>I</td>
<td>No annotation</td>
</tr>
<tr><td>Csi-miRN37</td>
<td>orange1.1 t02400</td>
<td>II</td>
<td>I</td>
<td>N/A</td>
<td>Indole-3-acetic acid-induced protein ARG7</td>
</tr>
</tbody>
</table>
<table-wrap-foot><p>N/A means not available in the degradome data. Target transcripts were divided into three classes. In category I, the miRNA-guided cleavage fragment was the most abundant tag matching the transcript; In category II, the miRNA-guided cleavage fragment was not the most abundant fragment; however, it still formed a clear peak in the T-plot. The remaining target transcripts were classified into category III.</p>
</table-wrap-foot>
</table-wrap>
</p>
<p>Of the novel miRNAs that were considered to be younger (recently evolved) than the conserved miRNAs, only three (csi-miRN2, csi-miRN11 and csi-miRN20) had common targets or homologous genes in all tissues. Most of the novel miRNAs appeared to target different transcripts in different tissues; for example, csi-miRN10 targeted <italic>Cs9g04330</italic>
in flower and <italic>Cs4g05310</italic>
in fruit (Additional file <xref rid="MOESM5" ref-type="media">5</xref>
c). These results suggested that the functions of novel miRNAs may differ in leaf, flower and fruit tissues and might fulfill a more specific role when compared with known and conserved miRNAs.</p>
</sec>
<sec id="Sec6"><title>Identification of secondary siRNAs in <italic>C. sinensis</italic>
</title>
<p>An in-house script was developed to predict secondary siRNAs that might be triggered by 22 nt miRNAs in citrus. After the prediction, we examined the abundances of the secondary siRNAs using sRNA sequencing data. Seven miRNAs were predicted to trigger the secondary siRNAs generation (see in Additional file <xref rid="MOESM7" ref-type="media">7</xref>
), four of them were identified in at least two tissues. Csi-miRN20 could be identified in all three tissues; csi-miR482a-3p in both leaves and fruits, csi-miR3954a and csi-miR482c in both leaves and flowers. Secondary siRNAs were named using the convention of “miRNA-target-serial number”; for example, csi-miR3954a-Cs1g09635.1-9 refers to the ninth phased siRNA generated from <italic>Cs1g09635.1</italic>
and triggered by csi-miR3954a. Moreover, we identified these secondary siRNAs’ target genes using degradome sequencing data (Additional files <xref rid="MOESM7" ref-type="media">7</xref>
and <xref rid="MOESM8" ref-type="media">8</xref>
). Most of the secondary siRNA and target pairs had a high penalty score and only a few targets were classified into categories I and II. The analysis indicated that Csi-miR3954a-Cs1g09635.1-9 targeted triose-phosphate transporter gene (category I), csi-miR482a-3p-Cs5g18480.1-18 targeted the cleavage and polyadenylation specificity factor (CPSF) gene (category I), and csi-miRN20-Cs3g05320.1-24 targeted a signal peptidase gene (category I). These findings suggest that these phased siRNAs may play regulatory roles in plant development.</p>
<p>Here, multiple lines of evidence suggest the existence of both conserved and orange-specific <italic>TAS</italic>
gene families. The homologous <italic>TAS3</italic>
gene (<italic>Cs9g01780</italic>
) was identified as a target of csi-miR390 in orange. This is consistent with previous studies from TAS1-4 genes in <italic>Arabidopsis</italic>
[<xref ref-type="bibr" rid="CR6">6</xref>
, <xref ref-type="bibr" rid="CR37">37</xref>
, <xref ref-type="bibr" rid="CR45">45</xref>
], MdTAS3 and MdTAS4 in apple [<xref ref-type="bibr" rid="CR46">46</xref>
]and TAS3 gene containing two miR390 binding sites in tobacco [<xref ref-type="bibr" rid="CR47">47</xref>
]. Noticeably, a potential orange-specific TAS gene targeted by cis-miR3954a was observed with multiple supports. Firstly, csi-miR3954a was a citrus-specific miRNA which showed abundant expression in all three tissues; Secondly, this miRNA was found to be 22 nt in length and was also found to contain a 5’U; this characteristic structure was believed to trigger phased siRNA biogenesis[<xref ref-type="bibr" rid="CR5">5</xref>
]; Thirdly, the target gene (<italic>Cs1g09635</italic>
) of csi-miR3954a could not be functionally annotated and was predicted to be a non-coding transcript; Fourthly, the secondary siRNAs, derived from csi-miR3954 target genes, were detected in the small RNA libraries. One of these secondary siRNAs, named csi-miR3954a-Cs1g09635.1-7, was abundant in leaf and flower and targeted <italic>Cs4g11930</italic>
. Therefore, we hypothesized that targets of csi-miR3954a are potential novel <italic>TAS</italic>
target genes. A further evidence to determine if this is dependent on RNA-dependent RNA polymerase (RDR) is difficult in sweet orange due to the lack of RDR mutants. A recent example in tobacco observed that the 22 nt nta-miR6019 targets the <italic>N</italic>
gene and triggers the generation of nta-siRNAI and nta-siRNAII which was dependent on RDR6 as well as nta-siR2142 (generated from tobacco <italic>TAS3</italic>
), and concluded that the target of nta-miR6019 might be a novel <italic>TAS</italic>
gene [<xref ref-type="bibr" rid="CR48">48</xref>
].</p>
</sec>
<sec id="Sec7"><title>The distruibution of miRNAs in the <italic>C. sinensis</italic>
genome</title>
<p>Both novel and known miRNAs were equally distributed in the citrus genome (Figure <xref rid="Fig3" ref-type="fig">3</xref>
); however, some members of conserved miRNA families were located in the same region of a single chromosome. For example, csi-miR169c and csi-miR169i were located in the same region of chromosome 2.<fig id="Fig3"><label>Figure 3</label>
<caption><p><bold>The distribution of pre-miRNAs in the</bold>
<bold><italic>C. sinensis</italic>
</bold>
<bold>genome.</bold>
Precursors of known miRNAs are shown as blue rectangle and precursors of novel miRNAs are shown as red rectangle. The width of rectangle indicated the length of the precursors while the height of oblong indicated the length of the chromosome/scaffold. The chromosome/scaffold and precursors scale are showed at the bottom of the figure. The chromosomal locations of the pre-miRNAs are indicated.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig3_HTML" id="d30e1359"></graphic>
</fig>
</p>
<p>We analyzed all simple sequence repeat (SSR) loci in the orange genome and examined their co-localization with pre-miRNAs. Overall, 69 csi-pre-miRNA were identified to co-localize with SSR region. 77.6% of the co-localized SSRs were binucleotide or trinucleotide sequences and the most frequent repeat unit was UA, consistent with the notion that most trinucleotide SSRs contain the base U in plants [<xref ref-type="bibr" rid="CR49">49</xref>
]. The longest SSR, consisting of (CUU)<sub>15</sub>
(45 nt), was located within the pre-miR396c sequence (Table <xref rid="Tab4" ref-type="table">4</xref>
). Notably, csi-miR396c had four precursors containing different sized trinucleotide SSRs. (CUU)<sub>4</sub>
, (CUU)<sub>5</sub>
and (CUU)<sub>3</sub>
were located within the pre-csi-miR396c-1, pre-csi-miR396c-3 and pre-csi-miR396c-4 sequences, respectively. To date, little is known about the functions of SSRs co-localized with pre-miRNAs. Here, the length of the (CUU)<sub>n</sub>
repeat influenced the shape of the loop in the secondary structures of the csi-miR396c precursors (Figure <xref rid="Fig4" ref-type="fig">4</xref>
). A previous report demonstrated that SSRs located in UTRs and introns can affect gene expression and expression level [<xref ref-type="bibr" rid="CR50">50</xref>
]. Interestingly, analysis of the maize zma-miR396 family showed that zma-miR396e and zma-miR396f bearing SSRs (CU)<sub>n</sub>
and (CUU)<sub>n</sub>
had similar expression pattern among different tissues which was distinctly different from the expression pattern of the other miR396 members without SSRs (expression data is form the publication of Zhang et al. [<xref ref-type="bibr" rid="CR51">51</xref>
]. Additional file <xref rid="MOESM9" ref-type="media">9</xref>
). Changes in the organization of the loop may directly influence the expression of mature miRNA and may cause unexpected changes in their evolution.<table-wrap id="Tab4"><label>Table 4</label>
<caption><p><bold>Numbers of Simple Sequence Repeats (SSRs) and their co-localization with pre-miRNAs in sweet orange</bold>
</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th>Repeat unit</th>
<th>Repeat type</th>
<th>Frequency of SSR region co-localize with pre-miRNAs</th>
</tr>
</thead>
<tbody><tr><td>A</td>
<td>Mononucleotide</td>
<td>1</td>
</tr>
<tr><td>G</td>
<td>Mononucleotide</td>
<td>1</td>
</tr>
<tr><td>T</td>
<td>Mononucleotide</td>
<td>5</td>
</tr>
<tr><td>AC</td>
<td>Dinucleotide</td>
<td>2</td>
</tr>
<tr><td>AG</td>
<td>Dinucleotide</td>
<td>5</td>
</tr>
<tr><td>AT</td>
<td>Dinucleotide</td>
<td>2</td>
</tr>
<tr><td>CT</td>
<td>Dinucleotide</td>
<td>3</td>
</tr>
<tr><td>GA</td>
<td>Dinucleotide</td>
<td>7</td>
</tr>
<tr><td>GT</td>
<td>Dinucleotide</td>
<td>1</td>
</tr>
<tr><td>TA</td>
<td>Dinucleotide</td>
<td>12</td>
</tr>
<tr><td>TC</td>
<td>Dinucleotide</td>
<td>3</td>
</tr>
<tr><td>AAG</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>ACA</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>ATA</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>ATT</td>
<td>Trinucleotide</td>
<td>3</td>
</tr>
<tr><td>CAG</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>CTT</td>
<td>Trinucleotide</td>
<td>7</td>
</tr>
<tr><td>GAT</td>
<td>Trinucleotide</td>
<td>2</td>
</tr>
<tr><td>GTG</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>TAA</td>
<td>Trinucleotide</td>
<td>5</td>
</tr>
<tr><td>TCA</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>TGC</td>
<td>Trinucleotide</td>
<td>1</td>
</tr>
<tr><td>TGG</td>
<td>Trinucleotide</td>
<td>2</td>
</tr>
<tr><td>TTC</td>
<td>Trinucleotide</td>
<td>5</td>
</tr>
<tr><td>CATG</td>
<td>Tetranucleotide</td>
<td>1</td>
</tr>
<tr><td>TCAT</td>
<td>Tetranucleotide</td>
<td>1</td>
</tr>
<tr><td>TGCA</td>
<td>Tetranucleotide</td>
<td>1</td>
</tr>
<tr><td>TTAA</td>
<td>Tetranucleotide</td>
<td>2</td>
</tr>
<tr><td>TTCT</td>
<td>Tetranucleotide</td>
<td>4</td>
</tr>
<tr><td>TTTG</td>
<td>Tetranucleotide</td>
<td>1</td>
</tr>
<tr><td>TATAAT</td>
<td>Hexanucleotide</td>
<td>2</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="Fig4"><label>Figure 4</label>
<caption><p><bold>Co-localization of pre-Csi-miR396c and simple sequence repeat (SSR).</bold>
The mature miR396c sequence is highlighted in yellow and the SSRs are highlighted in blue. The different secondary structures of pre-Csi-miR396c caused by the different number of SSR units are shown.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig4_HTML" id="d30e1752"></graphic>
</fig>
</p>
<p>Isoforms of miRNAs that originated from a long pre-miRNA (greater than 350 nt in length) were also identified. Csi-miR166j.1 and csi-miR166j.3 were derived from the same precursor and were positioned 195 nt apart. Similarly, csi-miR477d.1 andcsi-miR477d.2 were positioned 126 nt apart in the same precursor. However, the expression modes of the mature miRNAs originating from these two precursors were distinctly different. Csi-miR166j.1 and csi-miR166j.3 had extremely similar patterns of expression in different tissues and both the mature miRNAs were derived from 3’ strand of the miRNA-miRNA* duplexes (Additional file <xref rid="MOESM10" ref-type="media">10</xref>
a). In contrast, Csi-miR477d.1 and csi-miR477d.2 were produced from different strands of the duplexes, i.e., csi-miR477d.1-3p was produced from 3’ strand while csi-miR477d.2-5p was produced from 5’ strand of the duplexes (Additional file <xref rid="MOESM10" ref-type="media">10</xref>
b). A study in grapevine showed that miRC13 and miRC15 are located 224 nt apart on chromosome 17, but these two miRNAs exhibit different expression patterns [<xref ref-type="bibr" rid="CR52">52</xref>
].</p>
</sec>
<sec id="Sec8"><title>Characterization of highly expressed miRNAs in fruit</title>
<p>Candidate miRNAs that showed remarkably differential expression levels in fruit as revealed by the sequencing data were further confirmed by Quantitative RT-PCR (qRT-PCR) and RNA gel blotting analyses. Totally, 65 known- and 15 novel- miRNAs were chose for qRT-PCR confirmation; 55 of them (about two thirds) are consistent with the sequencing data (Additional files <xref rid="MOESM2" ref-type="media">2</xref>
and <xref rid="MOESM11" ref-type="media">11</xref>
). The results showed that csi-miR164, csi-miR3951, csi-miR477a-3p and csi-miRN31 have remarkably higher expression in fruits compared with other tissues. These results were verified by both qRT-PCR and RNA gel blotting (Figure <xref rid="Fig5" ref-type="fig">5</xref>
, Figure <xref rid="Fig6" ref-type="fig">6</xref>
and Additional file <xref rid="MOESM11" ref-type="media">11</xref>
). Two targets of csi-miR164 were identified in fruit; the first was annotated as a NAC transcription factor gene which was confirmed by 5’ RACE (Figure <xref rid="Fig7" ref-type="fig">7</xref>
) and the second was annotated as a thymidine diphospho-glucose 4-6-dehydratase gene. Csi-miR3951 also had two targets in fruit; the first was <italic>orange1.1 t05622</italic>
and the second was <italic>Cs1g06060</italic>
(verified by 5’ RACE, see in Figure <xref rid="Fig7" ref-type="fig">7</xref>
), which were annotated as polyubiquitin 12 and polyubiquitin 3, respectively. These targets may be involved in protein degradation. <italic>Cs6g19680</italic>
, which was annotated as the developmental protein SEPALLATA 2 (SEP2), was identified as a target of csi-miR477a-3p (degradome data). Targets of csi-miRN31 were not detected by the degradome analysis. The target prediction revealed that csi-miRN34 targeted transmembrane emp24 domain-containing gene.<fig id="Fig5"><label>Figure 5</label>
<caption><p><bold>Expression levels of selected known miRNAs in leaf, flower and fruit.</bold>
Total RNAs from mixed leaf, mixed flower and fruit in 170DAF were extracted for RNA gel blot analyses; reverse complement probes were used to detect the indicated miRNAs. U6 RNA or 5.8 s rRNA were used as loading controls. Two different genotypes of orange were used. Orange genotype 1 is a common sweet orange while genotype 2 is a red flesh orange. <bold>(a)</bold>
miR482d-5p.2 was specifically expressed in leaf. <bold>(b)</bold>
miR3954a and miR167b.2 were expressed at higher levels in flower than the other tissues; miR5179 was specifically expressed in flower <bold>(c)</bold>
miR3951 and miR164 were expressed at higher levels in fruit than the other tissues; miR477a-3p was specifically expressed in fruit. L1, leaf of orange genotype 1; L2, leaf of orange genotype 2; F1, flower of orange genotype 1; F2, flower of orange genotype 2; Fr1, fruit of orange genotype 1; Fr2, fruit of orange genotype 2.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig5_HTML" id="d30e1820"></graphic>
</fig>
</p>
<p>Expression pattern of the four potential miRNAs were then further investigated on eight stages of fruit development and ripening (Figure <xref rid="Fig8" ref-type="fig">8</xref>
). The expression pattern suggested three of them are probably involved in the regulation of fruit development and ripening. Both csi-miRN31 and csi-miR477a-3p may have important role in the color break stage (140 DAF). Csi-miR164 showed significantly higher expression level at the final stage (fruit ripening stage), with a steady increase in expression level during fruit ripening (170–230 DAF). In depth function of the former two miRNAs are now under progress in other research. This study focused on csi-miR164a which may have particular function at the fruit ripening stages. At this stage, sweet orange is undergoing maturation with extensive molecular repertoire on both transcriptional and posttranscriptional levels. Therefore, csi-miR164, as a known miRNA, may have new function in orange fruit ripening on posttranscriptional level.<fig id="Fig6"><label>Figure 6</label>
<caption><p><bold>Expression levels of selected novel miRNAs in leaf, flower and fruit.</bold>
Total RNAs from mixed leaf, mixed flower and fruit in 170DAF were extracted for RNA gel blot analysis. Reverse complement probes were used to detect specific miRNAs. U6 RNA was used as a loading control for each membrane. Two different genotypes of orange were used. Orange genotype 1 is a common sweet orange while genotype 2 is a red flesh orange. <bold>(a)</bold>
miRN03 and miRN36 were expressed at higher levels in leaf than flower or fruit. <bold>(b)</bold>
miRN08 was specifically expressed in flower. <bold>(c)</bold>
miRN31 was specifically expressed in fruit. L1, leaf of orange genotype 1; L2, leaf of orange genotype 2; F1, flower of orange genotype 1; F2, flower of orange genotype 2; Fr1, fruit of orange genotype 1; Fr2, fruit of orange genotype 2.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig6_HTML" id="d30e1846"></graphic>
</fig>
<fig id="Fig7"><label>Figure 7</label>
<caption><p><bold>Target validation of selected sweet orange miRNAs.</bold>
5’ RACE analysis was carried out for each selected target gene which identified by degradome sequencing. Arrows indicated the cleavage sites of targets and the numbers showed the frequency of the clones sequenced. The Cleavage sites outside of the displayed sequence are not shown.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig7_HTML" id="d30e1858"></graphic>
</fig>
<fig id="Fig8"><label>Figure 8</label>
<caption><p><bold>Expression pattern of four candidate miRNAs during fruit development and ripening.</bold>
Total RNAs were isolated from fruit samples at different developmental stages, ranging from 20–230 days after flowering (DAF). Reverse complement probes were used to detect specific miRNAs by RNA gel blotting. U4 and U6 were used as loading controls in qRT-PCR and RNA gel blot analyses, respectively. Data from the qRT-PCR experiments are represented as the mean plus SD of n = 3 biological replicates. Internal appearance of orange fruits during 8 developmental stages was shown at the bottom.</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig8_HTML" id="d30e1870"></graphic>
</fig>
</p>
</sec>
<sec id="Sec9"><title>Csi-mi164 functions via target a NAC transcription factor</title>
<p>As mentioned above, csi-miR164 was highly active during fruit ripening and 5’RACE analysis showed csi-miR164 targeted <italic>Cs5g10870</italic>
, a NAC transcription factor. To confirm the interaction between csi-miR164 and <italic>Cs5g10870</italic>
in orange fruit, we detected the expression level of <italic>Cs5g10870</italic>
by qRT-PCR at fruit developmental stages. As showed in Figure <xref rid="Fig9" ref-type="fig">9</xref>
a, the expression level of csi-miR164 and <italic>Cs5g10870</italic>
displayed complementary expression pattern. Furthermore, a transient expression system was used to confirm that csi-miR164 degraded <italic>Cs5g10870 in vivo</italic>
. Overexpression vectors of csi-miR164 and a control miRNA were constructed respectively. Target site of miR164 in <italic>Cs5g10870</italic>
and a modified target site (inactivated target site) were inserted into a green fluorescent protein (<italic>GFP</italic>
) gene overexpression vector respectively as shown in Figure <xref rid="Fig9" ref-type="fig">9</xref>
b. In this assays, we used <italic>Agrobacterium tumefaciens</italic>
infiltration to co-express csi-miR164, control miRNA, <italic>GFP</italic>
gene carrying target site and <italic>GFP</italic>
gene carrying modified target site pair by pair (Figure <xref rid="Fig9" ref-type="fig">9</xref>
c). As a result, csi-miR164 targeted the target region of <italic>Cs5g10870</italic>
and repressed the expression of GFP obviously (Figure <xref rid="Fig9" ref-type="fig">9</xref>
e).<fig id="Fig9"><label>Figure 9</label>
<caption><p><bold>Csi-miR164 targeted</bold>
<bold><italic>Cs5g10870</italic>
</bold>
<bold>was verified</bold>
<bold><italic>in vivo.</italic>
</bold>
<bold>(a)</bold>
Expression levels of mi164 and <italic>Cs5g10870</italic>
were detected during the fruit development by qRT-PCR. U4 and <italic>ACTIN</italic>
were used as loading controls in qRT-PCR Data from the qRT-PCR experiments are represented as the mean plus SD of n = 3 biological replicates. <bold>(b)</bold>
Four overexpression vectors were constructed for transient expression system in tobacco. Vector ox-miR164 overexpress csi-miR164, ox-miRCon overexpress a control miRNA, ox-10TS + GFP overexpress a <italic>GFP</italic>
gene carrying target site of miR164 in <italic>Cs5g10870</italic>
, ox-10MTS + GFP overexpress a <italic>GFP</italic>
gene carrying a modified target site. <bold>(c)</bold>
Vectors used in tobacco co-expression assays in each lane were shown in the table. <bold>(d)</bold>
Co-infiltrated leaves and control leaves were photographed at the 3rd day after infiltration under bright light. <bold>(e)</bold>
Same leaves were photographed at the 3rd day after infiltration under UV light (wavelength = 365 nm).</p>
</caption>
<graphic xlink:href="12864_2014_6413_Fig9_HTML" id="d30e1975"></graphic>
</fig>
</p>
<p><italic>Cs5g10870</italic>
was categorized as a NAC domain-containing transcription factor. Plant NAC transcription factor was one of the largest families involved in diverse biological processes [<xref ref-type="bibr" rid="CR53">53</xref>
–<xref ref-type="bibr" rid="CR56">56</xref>
]. More, recent publications reveal that NAC transcript factors function as regulators in fruit ripening. NACs in banana(<italic>MaNACs</italic>
) were supposed to be involved in banana fruit ripening by interaction with ethylene signaling components [<xref ref-type="bibr" rid="CR57">57</xref>
]. Interestingly, the transcripts of <italic>MaNAC4</italic>
decreased during banana ripening as well as <italic>Cs5g10870</italic>
decreased during orange ripening. So far in <italic>C. sinensis</italic>
, two NACs were reported and suggested to be related to fruit development, fruit senescence and fruit response to postharvest stresses [<xref ref-type="bibr" rid="CR58">58</xref>
, <xref ref-type="bibr" rid="CR59">59</xref>
]. As csi-miR164 was higher expressed in fruit and was more active at the late stages during the orange fruit development, we suggested that csi-miR164 might be involved as a regulator in orange ripening by interacting with a NAC transcription factor. Further functional investigations of csi-miR164 and <italic>Cs5g10870</italic>
are required to confirm this hypothesis.</p>
</sec>
</sec>
<sec id="Sec10" sec-type="conclusions"><title>Conclusions</title>
<p>Our study provides a genome-wide comparison of miRNAs and their target genes among leaf, flower and fruit of sweet orange with the aim of identification of regulators involved in fruit development and ripening. Comprehensive genome analysis uncovered 183 known- and 38 novel- miRNAs, and revealed their genomic characteristics such as isoform miRNAs, co-localization with SSR locus and secondary siRNAs. Comparative analysis showed that some known miRNAs, such as csi-miR168a and csi-miR159 in this study, may fulfill specific function in specific tissues via target different genes. This kind of tissue specific regulation was even obvious for novel miRNAs. Three miRNAs, csi-miRN31, csi-miR477a-3p and csi-164a, were identified to be highly expressed in fruit and probably important regulators of fruit ripening. Csi-miR164 was further validated to functions by target NAC transcription factor. The results of this study provide three promising miRNAs for understanding the posttranscriptional regulation of orange fruit development and ripening.</p>
</sec>
<sec id="Sec11" sec-type="methods"><title>Methods</title>
<sec id="Sec12"><title>Plant materials</title>
<p>The ‘Anliu’ sweet orange (<italic>C. sinensis</italic>
[L.] Osbeck) was planted at the Institute of Citrus Research located in Guilin, Guangxi Province, China. Leaves (young and mature stages) and flowers (early flower bud, flower bud and mature flower) used in sRNAome and degradome sequencing were mixed as a pool from three trees respectively. Fruit samples used in degradome sequencing were collected at 170 days after flowering (DAF) as previously published [<xref ref-type="bibr" rid="CR35">35</xref>
]. To detect the expression pattern of key miRNAs in the fruit development, we also collected fruit samples (from three trees as replicates) at developmental stages, including 20 DAF, 50 DAF, 80 DAF, 110 DAF, 140 DAF, 170 DAF, 200 DAF and 230 DAF. Fruit samples were separated into peel and pulp after collection. Pulp without seeds was used in all analysis in this research. All samples were frozen in liquid nitrogen immediately after collection and kept at -80°C until use. The <italic>Nicotiana benthamiana</italic>
was grown in a growth chamber controlled at 14 h light, 10 h dark, 25°C cycles.</p>
</sec>
<sec id="Sec13"><title>SRNAome sequencing and degradome sequencing</title>
<p>Total RNAs were extracted from different samples as Xu et al. described [<xref ref-type="bibr" rid="CR35">35</xref>
] and used in sRNAome sequencing and degradome sequencing. The sRNA libraries were constructed and sequenced for flower and leaf in this study, fruit sRNA data were derived from our published data with the same strategy [<xref ref-type="bibr" rid="CR35">35</xref>
]. Degradome sequencing strategy was applied to all the three tissues as described previously [<xref ref-type="bibr" rid="CR16">16</xref>
, <xref ref-type="bibr" rid="CR39">39</xref>
]. All these high-throughput sequencing were performed by Beijing Genomics Institute (BGI) (Shenzhen, China). The Illumina 1 G Genome Analyzer was used for the sRNA sequencing while the Illumina HiSeq 2000 was used for the degordome sequencing.</p>
</sec>
<sec id="Sec14"><title>Bioinformatic analysis</title>
<p>All sRNAome raw data were processed by removing adaptors, low quality tags as well as contaminants at pre-analysis. Then, the clean sRNA sequences were compared to the Rfam database (<ext-link ext-link-type="uri" xlink:href="http://rfam.sanger.ac.uk/">http://rfam.sanger.ac.uk/</ext-link>
) to exclude rRNA, tRNA, snRNA and snoRNA. The rest sRNA sequences were used to search known miRNAs by BLASTN against miRBase 16.0 (<ext-link ext-link-type="uri" xlink:href="http://www.mirbase.org/">http://www.mirbase.org/</ext-link>
). SRNAs with two or less mismatches compared to known miRNAs annotated in miRBase 16.0 were considered as known miRNAs in <italic>C. sinensis</italic>
. To identify novel miRNA, we performed a bioinformatics approach according to criteria described previously [<xref ref-type="bibr" rid="CR14">14</xref>
]. To predict the secondary structure of miRNAs, we used RNAfold in the Vienna RNA Package downloaded from vienna RNA web servers (<ext-link ext-link-type="uri" xlink:href="http://rna.tbi.univie.ac.at/">http://rna.tbi.univie.ac.at/</ext-link>
). Genome sequence of <italic>C. sinensis</italic>
annotated by our group (<ext-link ext-link-type="uri" xlink:href="http://citrus.hzau.edu.cn/orange/index.php">http://citrus.hzau.edu.cn/orange/index.php</ext-link>
) [<xref ref-type="bibr" rid="CR36">36</xref>
] was used as reference.</p>
<p>Degradome raw data was trimmed by pre-analysis as similar as sRNAome raw data. Then, clean degradome data were processed using the CleaveLand pipeline [<xref ref-type="bibr" rid="CR16">16</xref>
] (<ext-link ext-link-type="uri" xlink:href="http://axtell-lab-psu.weebly.com/cleaveland.html">http://axtell-lab-psu.weebly.com/cleaveland.html</ext-link>
). Subsequently, the transcripts targeted by miRNAs were grouped into three categories as previously reported [<xref ref-type="bibr" rid="CR39">39</xref>
].</p>
<p>To predict all potential secondary siRNA in orange, we performed a bioinformatics approach as follows. First of all, we obtained all miRNAs with length of 22 nt from sRNAome data and their target transcripts from degradome data. Then, 21 nt standard secondary siRNAs were generated from the cleavage site of target transcripts to 3’ end of targets one by one. We named secondary siRNA as miRNA-target-serial number. Such as csi-miR3954a-Cs1g09635.1-9, which meant the ninth phased siRNA generated form Cs1g09635.1 and triggered by csi-miR3954a. Finally, we could obtain the digital expressions (TPM) of these secondary siRNAs from the sRNAome data and target transcripts of these secondary siRNAs from degradome data through CleaveLand pipeline (Flow chart see in Additional file <xref rid="MOESM12" ref-type="media">12</xref>
).</p>
</sec>
<sec id="Sec15"><title>qRT-PCR and RNA gel blotting analyses</title>
<p>To confirm miRNAs’ expression, stem-loop qRT-PCR and RNA gel blot analysis were both used in our research. RNAs used in both experiments were the same as RNAs used in high-throughput sequencing.</p>
<p>Stem-loop qRT-PCR was described to be a highly sensitive method for detection of miRNAs [<xref ref-type="bibr" rid="CR60">60</xref>
, <xref ref-type="bibr" rid="CR61">61</xref>
]. We performed stem-loop qRT-PCR mainly according to previous publication in three biological replicates. All primers used in qRT-PCR analysis were provided in Additional file <xref rid="MOESM13" ref-type="media">13</xref>
. Additionally, we improved a much more efficient loading control gene U4 instead of traditional U6 as Kou et al. described [<xref ref-type="bibr" rid="CR62">62</xref>
]. U4 showed more stably expressed at leaves, flowers and fruit samples at developmental stages of ‘Anliu’ sweet orange than U6 after experiment.</p>
<p>For RNA gel blot analysis, 10 μg total RNA from different samples were loaded to a denaturing 15% polyacrylamide gel and transferred to Hybond-N + membranes (Amersham, GE Healthcare). The membranes were cross linked by ultraviolet cross linker and then used for bloting. Reverse complement DNA oligonucletides were used as probes to detect specific miRNAs. Probes were labeled the by Biotin 3’ End DNA Labeling Kit (Thermo) and then used for bloting. Chemiluminescent Hybridization and Detection Kit (Thermo) were used for hybridization and signal detection. At the beginning, 5.8 s rRNA was used as a loading control. Instead, U6 was used as a loading control later.</p>
</sec>
<sec id="Sec16"><title>5’ RACE</title>
<p>RNA Ligase-Mediated 5’ RACE (RLM-RACE) was performed with the GeneRacer kit (Invitrogen) as described in the product manual. Briefly, 10 μg total RNA was ligated to the 5’ adaptor. The ligated mRNA was reverse transcribed by oligo (dT) primer. To obtain the 5’ end products, PCR was proformed using 5’ adaptor primers and 3’ gene-specific primers. Finally, the products were cloned, sequenced and analysed.</p>
</sec>
<sec id="Sec17"><title>Transient expression system in tobacco</title>
<p>To verify the interaction between miRNAs and their targets <italic>in vivo</italic>
, we used <italic>Agrobacterium tumefaciens</italic>
infiltration to co-express miRNAs and their targets in tobacco. Transient expression in tobacco was applied as described previously [<xref ref-type="bibr" rid="CR63">63</xref>
].</p>
</sec>
</sec>
<sec id="Sec18"><title>Availability of supporting data</title>
<p>The sRNA sequence data and the degradome data supporting the results of this article have been submitted to Gene Expression Omnibus (GEO) under accession NO. GSE46765 and GSE18207 at website: <ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?token=bvcnfememqckehi&acc=GSE46765">http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?token=bvcnfememqckehi&acc=GSE46765</ext-link>
and <ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?token=bvcnfememqckehi&acc=GSE18207">http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?token=bvcnfememqckehi&acc=GSE18207</ext-link>
.</p>
<p>Accession NO. GSE46765 will be released on Dec 30, 2014.</p>
</sec>
<sec sec-type="supplementary-material"><title>Electronic supplementary material</title>
<sec id="Sec19"><supplementary-material content-type="local-data" id="MOESM1"><media xlink:href="12864_2014_6413_MOESM1_ESM.pdf"><caption><p>Additional file 1:
<bold>Predicted secondary structures of known and novel miRNAs.</bold>
The mature miRNA sequences are highlighted in yellow. For novel miRNAs, the miRNA* sequences are highlighted in gray. (PDF 4 MB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM2"><media xlink:href="12864_2014_6413_MOESM2_ESM.pdf"><caption><p>Additional file 2:
<bold>Normalized count of all miRNAs in orange leaf, flower and fruit.</bold>
(PDF 19 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM3"><media xlink:href="12864_2014_6413_MOESM3_ESM.pdf"><caption><p>Additional file 3:
<bold>Targets of miRNAs identified using degradome sequencing.</bold>
(PDF 28 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM4"><media xlink:href="12864_2014_6413_MOESM4_ESM.pdf"><caption><p>Additional file 4:
<bold>T-plots of the miRNA targets in different tissues.</bold>
Densities of the 5’ positions of degradome tags matching each target gene are shown as T-plots. The miRNA-mediated degradome tag is highlighted in red. (PDF 14 MB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM5"><media xlink:href="12864_2014_6413_MOESM5_ESM.pdf"><caption><p>Additional file 5:
<bold>T-plots of diverse targets of miRNAs in different tissues.</bold>
Densities of the 5’ positions of degradome tags matching each target gene are shown as T-plots. The miRNA-mediated degradome tag is highlighted in red. (a) miR168a targets <italic>AGO1</italic>
in all three tissues; additionally, miR168a targets CUC2 in leaf and a pantothenate kinase gene in fruit; (b) miR159 targets GAMYB in leaf and flower; but it targets DRT100 in fruit; (c) miRN10 targets different transcripts in flower and fruit. (PDF 552 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM6"><media xlink:href="12864_2014_6413_MOESM6_ESM.pdf"><caption><p>Additional file 6:
<bold>Annotations of all target genes.</bold>
(PDF 153 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM7"><media xlink:href="12864_2014_6413_MOESM7_ESM.pdf"><caption><p>Additional file 7:
<bold>Normalized count of secondary siRNAs and their targets identified using degradome sequencing.</bold>
(PDF 36 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM8"><media xlink:href="12864_2014_6413_MOESM8_ESM.pdf"><caption><p>Additional file 8:
<bold>T-plots of the targets of secondary siRNAs in different tissues.</bold>
Densities of the 5’ positions of degradome tags matching each target gene are shown as T-plots. The miRNA mediated degradome tag is highlighted in red. (PDF 4 MB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM9"><media xlink:href="12864_2014_6413_MOESM9_ESM.pdf"><caption><p>Additional file 9:
<bold>Comparative analysis of the presence of SSRs in zma-miR396 and the resulting expression pattern among different tissues in maize.</bold>
Sequences data were collected from miRBase, the expression data were come from the publication of Zhang et al. (PDF 488 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM10"><media xlink:href="12864_2014_6413_MOESM10_ESM.pdf"><caption><p>Additional file 10:
<bold>Clusters of miRNAs.</bold>
Two miRNAs located within a single precursor are shown. The mature miRNA sequences are highlighted in yellow and the miRNA* sequences are highlighted in gray. The mismatched nucleotide is highlighted in red. Data in the tables show the digital expression levels (TPM) of miRNAs in different tissues. (a) Csi-miR166j.1 and Csi-miR166j.3. (b) Csi-miR477d.1-3p and Csi-miR477d.2-5p. (PDF 615 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM11"><media xlink:href="12864_2014_6413_MOESM11_ESM.pdf"><caption><p>Additional file 11:
<bold>Confirmation of the expression levels of 80 selected miRNAs in different tissues by qRT-PCR.</bold>
A total of 65 known miRNAs and 15 novel miRNAs were selected according to their differential expression in leaf (L), flower (F) and fruit (Fr), which was derived from high-throughput sequencing. The expression levels of these miRNAs were confirmed using stem-loop qRT-PCR. U4 was used as a loading control gene in qRT-PCR. The data are represented as the mean plus SD of n = 3 biological replicates. (PDF 2 MB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM12"><media xlink:href="12864_2014_6413_MOESM12_ESM.pdf"><caption><p>Additional file 12:
<bold>Flow chart to identify the phased siRNAs and their target transcripts.</bold>
(PDF 227 KB)</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="MOESM13"><media xlink:href="12864_2014_6413_MOESM13_ESM.pdf"><caption><p>Additional file 13:
<bold>Primers used in miRNA stem-loop RT-PCR.</bold>
(PDF 38 KB)</p>
</caption>
</media>
</supplementary-material>
</sec>
</sec>
</body>
<back><glossary><title>Abbreviations</title>
<def-list><def-list><def-item><term>AGO</term>
<def><p>Argonaute protein</p>
</def>
</def-item>
<def-item><term>miRNA</term>
<def><p>Micro RNA</p>
</def>
</def-item>
<def-item><term>nt</term>
<def><p>Nucleotide</p>
</def>
</def-item>
<def-item><term>pri-miRNA</term>
<def><p>Primary miRNA</p>
</def>
</def-item>
<def-item><term>per-miRNA</term>
<def><p>Precursor of miRNA</p>
</def>
</def-item>
<def-item><term>RISC</term>
<def><p>RNA-induced silencing complex</p>
</def>
</def-item>
<def-item><term>RDR6</term>
<def><p>RNA-dependent RNA polymerase</p>
</def>
</def-item>
<def-item><term>sRNA</term>
<def><p>Small RNA</p>
</def>
</def-item>
<def-item><term>SSR</term>
<def><p>Simple sequence repeat</p>
</def>
</def-item>
<def-item><term>tasiRNA</term>
<def><p>Trans-acting siRNA.</p>
</def>
</def-item>
</def-list>
</def-list>
</glossary>
<fn-group><fn><p><bold>Competing interests</bold>
</p>
<p>The authors declare that they have no competing interests.</p>
</fn>
<fn><p><bold>Authors’ contributions</bold>
</p>
<p>XQ and DXX conceived the project. XQ supervised the project. LYL carried out the experiments and performed data analysis and wrote the manuscript. XQ and LL contributed to the writing. WL performed the degradome analysis and developed the bioinformatics approach to predict secondary siRNA together with LYL. CDJ and CLL performed the miRNA predictions. WXM along with LYL modified the Northern blot analysis. HD carried out the qRT-PCR. All authors read and approved the final manuscript.</p>
</fn>
</fn-group>
<ack><title>Acknowledgements</title>
<p>This project was supported by the the Ministry of Science and Technology of China (2011CB100601) and the National Natural Science Foundation of China (31272148 and 31222047).</p>
</ack>
<ref-list id="Bib1"><title>References</title>
<ref id="CR1"><label>1.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>MicroRNAs: genomics, biogenesis, mechanism, and function</article-title>
<source>Cell</source>
<year>2004</year>
<volume>116</volume>
<fpage>281</fpage>
<lpage>297</lpage>
<pub-id pub-id-type="doi">10.1016/S0092-8674(04)00045-5</pub-id>
<pub-id pub-id-type="pmid">14744438</pub-id>
</element-citation>
</ref>
<ref id="CR2"><label>2.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wang</surname>
<given-names>H</given-names>
</name>
<name><surname>Zhang</surname>
<given-names>X</given-names>
</name>
<name><surname>Liu</surname>
<given-names>J</given-names>
</name>
<name><surname>Kiba</surname>
<given-names>T</given-names>
</name>
<name><surname>Woo</surname>
<given-names>J</given-names>
</name>
<name><surname>Ojo</surname>
<given-names>T</given-names>
</name>
<name><surname>Hafner</surname>
<given-names>M</given-names>
</name>
<name><surname>Tuschl</surname>
<given-names>T</given-names>
</name>
<name><surname>Chua</surname>
<given-names>NH</given-names>
</name>
<name><surname>Wang</surname>
<given-names>XJ</given-names>
</name>
</person-group>
<article-title>Deep sequencing of small RNAs specifically associated with <italic>Arabidopsis</italic>
AGO1 and AGO4 uncovers new AGO functions</article-title>
<source>Plant J</source>
<year>2011</year>
<volume>67</volume>
<fpage>292</fpage>
<lpage>304</lpage>
<pub-id pub-id-type="doi">10.1111/j.1365-313X.2011.04594.x</pub-id>
<pub-id pub-id-type="pmid">21457371</pub-id>
</element-citation>
</ref>
<ref id="CR3"><label>3.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kim</surname>
<given-names>VN</given-names>
</name>
</person-group>
<article-title>Sorting out small RNAs</article-title>
<source>Cell</source>
<year>2008</year>
<volume>133</volume>
<fpage>25</fpage>
<lpage>26</lpage>
<pub-id pub-id-type="doi">10.1016/j.cell.2008.03.015</pub-id>
<pub-id pub-id-type="pmid">18394983</pub-id>
</element-citation>
</ref>
<ref id="CR4"><label>4.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Jin</surname>
<given-names>HL</given-names>
</name>
<name><surname>Zhang</surname>
<given-names>XM</given-names>
</name>
<name><surname>Zhao</surname>
<given-names>HW</given-names>
</name>
<name><surname>Gao</surname>
<given-names>S</given-names>
</name>
<name><surname>Wang</surname>
<given-names>WC</given-names>
</name>
<name><surname>Katiyar-Agarwal</surname>
<given-names>S</given-names>
</name>
<name><surname>Huang</surname>
<given-names>HD</given-names>
</name>
<name><surname>Raikhel</surname>
<given-names>N</given-names>
</name>
</person-group>
<article-title><italic>Arabidopsis</italic>
Argonaute 2 Regulates Innate Immunity via miRNA393*-Mediated Silencing of a Golgi-Localized SNARE Gene, <italic>MEMB12</italic>
</article-title>
<source>Mol Cell</source>
<year>2011</year>
<volume>42</volume>
<fpage>356</fpage>
<lpage>366</lpage>
<pub-id pub-id-type="doi">10.1016/j.molcel.2011.04.010</pub-id>
<pub-id pub-id-type="pmid">21549312</pub-id>
</element-citation>
</ref>
<ref id="CR5"><label>5.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chen</surname>
<given-names>HM</given-names>
</name>
<name><surname>Chen</surname>
<given-names>LT</given-names>
</name>
<name><surname>Patel</surname>
<given-names>K</given-names>
</name>
<name><surname>Li</surname>
<given-names>YH</given-names>
</name>
<name><surname>Baulcombe</surname>
<given-names>DC</given-names>
</name>
<name><surname>Wu</surname>
<given-names>SH</given-names>
</name>
</person-group>
<article-title>22-Nucleotide RNAs trigger secondary siRNA biogenesis in plants</article-title>
<source>Proc Natl Acad Sci U S A</source>
<year>2010</year>
<volume>107</volume>
<fpage>15269</fpage>
<lpage>15274</lpage>
<pub-id pub-id-type="doi">10.1073/pnas.1001738107</pub-id>
<pub-id pub-id-type="pmid">20643946</pub-id>
</element-citation>
</ref>
<ref id="CR6"><label>6.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Allen</surname>
<given-names>E</given-names>
</name>
<name><surname>Howell</surname>
<given-names>MD</given-names>
</name>
</person-group>
<article-title>miRNAs in the biogenesis of trans-acting siRNAs in higher plants</article-title>
<source>Semin Cell Dev Biol</source>
<year>2010</year>
<volume>21</volume>
<fpage>798</fpage>
<lpage>804</lpage>
<pub-id pub-id-type="doi">10.1016/j.semcdb.2010.03.008</pub-id>
<pub-id pub-id-type="pmid">20359543</pub-id>
</element-citation>
</ref>
<ref id="CR7"><label>7.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Axtell</surname>
<given-names>MJ</given-names>
</name>
<name><surname>Jan</surname>
<given-names>C</given-names>
</name>
<name><surname>Rajagopalan</surname>
<given-names>R</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>A two-hit trigger for siRNA biogenesis in plants</article-title>
<source>Cell</source>
<year>2006</year>
<volume>127</volume>
<fpage>565</fpage>
<lpage>577</lpage>
<pub-id pub-id-type="doi">10.1016/j.cell.2006.09.032</pub-id>
<pub-id pub-id-type="pmid">17081978</pub-id>
</element-citation>
</ref>
<ref id="CR8"><label>8.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Axtell</surname>
<given-names>MJ</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>Antiquity of microRNAs and their targets in land plants</article-title>
<source>Plant Cell</source>
<year>2005</year>
<volume>17</volume>
<fpage>1658</fpage>
<lpage>1673</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.105.032185</pub-id>
<pub-id pub-id-type="pmid">15849273</pub-id>
</element-citation>
</ref>
<ref id="CR9"><label>9.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Karlova</surname>
<given-names>R</given-names>
</name>
<name><surname>van Haarst</surname>
<given-names>JC</given-names>
</name>
<name><surname>Maliepaard</surname>
<given-names>C</given-names>
</name>
<name><surname>van de Geest</surname>
<given-names>H</given-names>
</name>
<name><surname>Bovy</surname>
<given-names>AG</given-names>
</name>
<name><surname>Lammers</surname>
<given-names>M</given-names>
</name>
<name><surname>Angenent</surname>
<given-names>GC</given-names>
</name>
<name><surname>de Maagd</surname>
<given-names>RA</given-names>
</name>
</person-group>
<article-title>Identification of microRNA targets in tomato fruit development using high-throughput sequencing and degradome analysis</article-title>
<source>J Exp Bot</source>
<year>2013</year>
<volume>64</volume>
<fpage>1863</fpage>
<lpage>1878</lpage>
<pub-id pub-id-type="doi">10.1093/jxb/ert049</pub-id>
<pub-id pub-id-type="pmid">23487304</pub-id>
</element-citation>
</ref>
<ref id="CR10"><label>10.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wang</surname>
<given-names>C</given-names>
</name>
<name><surname>Han</surname>
<given-names>J</given-names>
</name>
<name><surname>Liu</surname>
<given-names>CH</given-names>
</name>
<name><surname>Kibet</surname>
<given-names>KN</given-names>
</name>
<name><surname>Kayesh</surname>
<given-names>E</given-names>
</name>
<name><surname>Shangguan</surname>
<given-names>LF</given-names>
</name>
<name><surname>Li</surname>
<given-names>XY</given-names>
</name>
<name><surname>Fang</surname>
<given-names>JG</given-names>
</name>
</person-group>
<article-title>Identification of microRNAs from Amur grape (vitis amurensis Rupr) by deep sequencing and analysis of microRNA variations with bioinformatics</article-title>
<source>BMC Genomics</source>
<year>2012</year>
<volume>13</volume>
<fpage>122</fpage>
<pub-id pub-id-type="doi">10.1186/1471-2164-13-122</pub-id>
<pub-id pub-id-type="pmid">22455456</pub-id>
</element-citation>
</ref>
<ref id="CR11"><label>11.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Aryal</surname>
<given-names>R</given-names>
</name>
<name><surname>Jagadeeswaran</surname>
<given-names>G</given-names>
</name>
<name><surname>Zheng</surname>
<given-names>Y</given-names>
</name>
<name><surname>Yu</surname>
<given-names>QY</given-names>
</name>
<name><surname>Sunkar</surname>
<given-names>R</given-names>
</name>
<name><surname>Ming</surname>
<given-names>R</given-names>
</name>
</person-group>
<article-title>Sex specific expression and distribution of small RNAs in papaya</article-title>
<source>BMC Genomics</source>
<year>2014</year>
<volume>15</volume>
<fpage>20</fpage>
<pub-id pub-id-type="doi">10.1186/1471-2164-15-20</pub-id>
<pub-id pub-id-type="pmid">24410969</pub-id>
</element-citation>
</ref>
<ref id="CR12"><label>12.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Xu</surname>
<given-names>L</given-names>
</name>
<name><surname>Wang</surname>
<given-names>Y</given-names>
</name>
<name><surname>Xu</surname>
<given-names>YY</given-names>
</name>
<name><surname>Wang</surname>
<given-names>LJ</given-names>
</name>
<name><surname>Zhai</surname>
<given-names>LL</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>XW</given-names>
</name>
<name><surname>Gong</surname>
<given-names>YQ</given-names>
</name>
<name><surname>Ye</surname>
<given-names>S</given-names>
</name>
<name><surname>Liu</surname>
<given-names>LW</given-names>
</name>
</person-group>
<article-title>Identification and characterization of novel and conserved microRNAs in radish (Raphanus sativus L.) using high-throughput sequencing</article-title>
<source>Plant Sci</source>
<year>2013</year>
<volume>201</volume>
<fpage>108</fpage>
<lpage>114</lpage>
<pub-id pub-id-type="doi">10.1016/j.plantsci.2012.11.010</pub-id>
<pub-id pub-id-type="pmid">23352408</pub-id>
</element-citation>
</ref>
<ref id="CR13"><label>13.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname>
<given-names>X-N</given-names>
</name>
<name><surname>Li</surname>
<given-names>X</given-names>
</name>
<name><surname>Liu</surname>
<given-names>J-H</given-names>
</name>
</person-group>
<article-title>Identification of Conserved and Novel Cold-Responsive MicroRNAs in Trifoliate Orange (Poncirus trifoliata (L.) Raf.) Using High-Throughput Sequencing</article-title>
<source>Plant Mol Biol Rep</source>
<year>2014</year>
<volume>32</volume>
<fpage>328</fpage>
<lpage>341</lpage>
<pub-id pub-id-type="doi">10.1007/s11105-013-0649-1</pub-id>
</element-citation>
</ref>
<ref id="CR14"><label>14.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Meyers</surname>
<given-names>BC</given-names>
</name>
<name><surname>Axtell</surname>
<given-names>MJ</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>B</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
<name><surname>Baulcombe</surname>
<given-names>D</given-names>
</name>
<name><surname>Bowman</surname>
<given-names>JL</given-names>
</name>
<name><surname>Cao</surname>
<given-names>X</given-names>
</name>
<name><surname>Carrington</surname>
<given-names>JC</given-names>
</name>
<name><surname>Chen</surname>
<given-names>XM</given-names>
</name>
<name><surname>Green</surname>
<given-names>PJ</given-names>
</name>
<name><surname>Griffiths-Jones</surname>
<given-names>S</given-names>
</name>
<name><surname>Jacobsen</surname>
<given-names>SE</given-names>
</name>
<name><surname>Mallory</surname>
<given-names>AC</given-names>
</name>
<name><surname>Martienssen</surname>
<given-names>RA</given-names>
</name>
<name><surname>Poethig</surname>
<given-names>RS</given-names>
</name>
<name><surname>Qi</surname>
<given-names>Y</given-names>
</name>
<name><surname>Vaucheret</surname>
<given-names>H</given-names>
</name>
<name><surname>Voinnet</surname>
<given-names>O</given-names>
</name>
<name><surname>Watanabe</surname>
<given-names>Y</given-names>
</name>
<name><surname>Weigel</surname>
<given-names>D</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>JK</given-names>
</name>
</person-group>
<article-title>Criteria for Annotation of Plant MicroRNAs</article-title>
<source>Plant Cell</source>
<year>2008</year>
<volume>20</volume>
<fpage>3186</fpage>
<lpage>3190</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.108.064311</pub-id>
<pub-id pub-id-type="pmid">19074682</pub-id>
</element-citation>
</ref>
<ref id="CR15"><label>15.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>German</surname>
<given-names>MA</given-names>
</name>
<name><surname>Pillay</surname>
<given-names>M</given-names>
</name>
<name><surname>Jeong</surname>
<given-names>DH</given-names>
</name>
<name><surname>Hetawal</surname>
<given-names>A</given-names>
</name>
<name><surname>Luo</surname>
<given-names>S</given-names>
</name>
<name><surname>Janardhanan</surname>
<given-names>P</given-names>
</name>
<name><surname>Kannan</surname>
<given-names>V</given-names>
</name>
<name><surname>Rymarquis</surname>
<given-names>LA</given-names>
</name>
<name><surname>Nobuta</surname>
<given-names>K</given-names>
</name>
<name><surname>German</surname>
<given-names>R</given-names>
</name>
<name><surname>De Paoli</surname>
<given-names>E</given-names>
</name>
<name><surname>Lu</surname>
<given-names>C</given-names>
</name>
<name><surname>Schroth</surname>
<given-names>G</given-names>
</name>
<name><surname>Meyers</surname>
<given-names>BC</given-names>
</name>
<name><surname>Green</surname>
<given-names>PJ</given-names>
</name>
</person-group>
<article-title>Global identification of microRNA-target RNA pairs by parallel analysis of RNA ends</article-title>
<source>Nat Biotechnol</source>
<year>2008</year>
<volume>26</volume>
<fpage>941</fpage>
<lpage>946</lpage>
<pub-id pub-id-type="doi">10.1038/nbt1417</pub-id>
<pub-id pub-id-type="pmid">18542052</pub-id>
</element-citation>
</ref>
<ref id="CR16"><label>16.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Addo-Quaye</surname>
<given-names>C</given-names>
</name>
<name><surname>Miller</surname>
<given-names>W</given-names>
</name>
<name><surname>Axtell</surname>
<given-names>MJ</given-names>
</name>
</person-group>
<article-title>CleaveLand: a pipeline for using degradome data to find cleaved small RNA targets</article-title>
<source>Bioinformatics</source>
<year>2009</year>
<volume>25</volume>
<fpage>130</fpage>
<lpage>131</lpage>
<pub-id pub-id-type="doi">10.1093/bioinformatics/btn604</pub-id>
<pub-id pub-id-type="pmid">19017659</pub-id>
</element-citation>
</ref>
<ref id="CR17"><label>17.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>German</surname>
<given-names>MA</given-names>
</name>
<name><surname>Luo</surname>
<given-names>S</given-names>
</name>
<name><surname>Schroth</surname>
<given-names>G</given-names>
</name>
<name><surname>Meyers</surname>
<given-names>BC</given-names>
</name>
<name><surname>Green</surname>
<given-names>PJ</given-names>
</name>
</person-group>
<article-title>Construction of Parallel Analysis of RNA Ends (PARE) libraries for the study of cleaved miRNA targets and the RNA degradome</article-title>
<source>Nat Protoc</source>
<year>2009</year>
<volume>4</volume>
<fpage>356</fpage>
<lpage>362</lpage>
<pub-id pub-id-type="doi">10.1038/nprot.2009.8</pub-id>
<pub-id pub-id-type="pmid">19247285</pub-id>
</element-citation>
</ref>
<ref id="CR18"><label>18.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Garcia</surname>
<given-names>D</given-names>
</name>
</person-group>
<article-title>A miRacle in plant development: role of microRNAs in cell differentiation and patterning</article-title>
<source>Semin Cell Dev Biol</source>
<year>2008</year>
<volume>19</volume>
<fpage>586</fpage>
<lpage>595</lpage>
<pub-id pub-id-type="doi">10.1016/j.semcdb.2008.07.013</pub-id>
<pub-id pub-id-type="pmid">18708151</pub-id>
</element-citation>
</ref>
<ref id="CR19"><label>19.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chuck</surname>
<given-names>G</given-names>
</name>
<name><surname>O'Connor</surname>
<given-names>D</given-names>
</name>
</person-group>
<article-title>Small RNAs going the distance during plant development</article-title>
<source>Curr Opin Plant Biol</source>
<year>2010</year>
<volume>13</volume>
<fpage>40</fpage>
<lpage>45</lpage>
<pub-id pub-id-type="doi">10.1016/j.pbi.2009.08.006</pub-id>
<pub-id pub-id-type="pmid">19796985</pub-id>
</element-citation>
</ref>
<ref id="CR20"><label>20.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Juarez</surname>
<given-names>MT</given-names>
</name>
<name><surname>Kui</surname>
<given-names>JS</given-names>
</name>
<name><surname>Thomas</surname>
<given-names>J</given-names>
</name>
<name><surname>Heller</surname>
<given-names>BA</given-names>
</name>
<name><surname>Timmermans</surname>
<given-names>MC</given-names>
</name>
</person-group>
<article-title>microRNA-mediated repression of rolled leaf1 specifies maize leaf polarity</article-title>
<source>Nature</source>
<year>2004</year>
<volume>428</volume>
<fpage>84</fpage>
<lpage>88</lpage>
<pub-id pub-id-type="doi">10.1038/nature02363</pub-id>
<pub-id pub-id-type="pmid">14999285</pub-id>
</element-citation>
</ref>
<ref id="CR21"><label>21.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Schwab</surname>
<given-names>R</given-names>
</name>
<name><surname>Palatnik</surname>
<given-names>JF</given-names>
</name>
<name><surname>Riester</surname>
<given-names>M</given-names>
</name>
<name><surname>Schommer</surname>
<given-names>C</given-names>
</name>
<name><surname>Schmid</surname>
<given-names>M</given-names>
</name>
<name><surname>Weigel</surname>
<given-names>D</given-names>
</name>
</person-group>
<article-title>Specific effects of microRNAs on the plant transcriptome</article-title>
<source>Dev Cell</source>
<year>2005</year>
<volume>8</volume>
<fpage>517</fpage>
<lpage>527</lpage>
<pub-id pub-id-type="doi">10.1016/j.devcel.2005.01.018</pub-id>
<pub-id pub-id-type="pmid">15809034</pub-id>
</element-citation>
</ref>
<ref id="CR22"><label>22.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Nikovics</surname>
<given-names>K</given-names>
</name>
<name><surname>Blein</surname>
<given-names>T</given-names>
</name>
<name><surname>Peaucelle</surname>
<given-names>A</given-names>
</name>
<name><surname>Ishida</surname>
<given-names>T</given-names>
</name>
<name><surname>Morin</surname>
<given-names>H</given-names>
</name>
<name><surname>Aida</surname>
<given-names>M</given-names>
</name>
<name><surname>Laufs</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>The balance between the <italic>MIR164A</italic>
and <italic>CUC2</italic>
genes controls leaf margin serration in <italic>Arabidopsis</italic>
</article-title>
<source>Plant Cell</source>
<year>2006</year>
<volume>18</volume>
<fpage>2929</fpage>
<lpage>2945</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.106.045617</pub-id>
<pub-id pub-id-type="pmid">17098808</pub-id>
</element-citation>
</ref>
<ref id="CR23"><label>23.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Berger</surname>
<given-names>Y</given-names>
</name>
<name><surname>Harpaz-Saad</surname>
<given-names>S</given-names>
</name>
<name><surname>Brand</surname>
<given-names>A</given-names>
</name>
<name><surname>Melnik</surname>
<given-names>H</given-names>
</name>
<name><surname>Sirding</surname>
<given-names>N</given-names>
</name>
<name><surname>Alvarez</surname>
<given-names>JP</given-names>
</name>
<name><surname>Zinder</surname>
<given-names>M</given-names>
</name>
<name><surname>Samach</surname>
<given-names>A</given-names>
</name>
<name><surname>Eshed</surname>
<given-names>Y</given-names>
</name>
<name><surname>Ori</surname>
<given-names>N</given-names>
</name>
</person-group>
<article-title>The NAC-domain transcription factor GOBLET specifies leaflet boundaries in compound tomato leaves</article-title>
<source>Development</source>
<year>2009</year>
<volume>136</volume>
<fpage>823</fpage>
<lpage>832</lpage>
<pub-id pub-id-type="doi">10.1242/dev.031625</pub-id>
<pub-id pub-id-type="pmid">19176589</pub-id>
</element-citation>
</ref>
<ref id="CR24"><label>24.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bertolini</surname>
<given-names>E</given-names>
</name>
<name><surname>Verelst</surname>
<given-names>W</given-names>
</name>
<name><surname>Horner</surname>
<given-names>DS</given-names>
</name>
<name><surname>Gianfranceschi</surname>
<given-names>L</given-names>
</name>
<name><surname>Piccolo</surname>
<given-names>V</given-names>
</name>
<name><surname>Inze</surname>
<given-names>D</given-names>
</name>
<name><surname>Pe</surname>
<given-names>ME</given-names>
</name>
<name><surname>Mica</surname>
<given-names>E</given-names>
</name>
</person-group>
<article-title>Addressing the role of microRNAs in reprogramming leaf growth during drought stress in Brachypodium distachyon</article-title>
<source>Mol Plant</source>
<year>2013</year>
<volume>6</volume>
<fpage>423</fpage>
<lpage>443</lpage>
<pub-id pub-id-type="doi">10.1093/mp/sss160</pub-id>
<pub-id pub-id-type="pmid">23264558</pub-id>
</element-citation>
</ref>
<ref id="CR25"><label>25.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Millar</surname>
<given-names>AA</given-names>
</name>
<name><surname>Gubler</surname>
<given-names>F</given-names>
</name>
</person-group>
<article-title>The Arabidopsis GAMYB-like genes, MYB33 and MYB65, are microRNA-regulated genes that redundantly facilitate anther development</article-title>
<source>Plant Cell</source>
<year>2005</year>
<volume>17</volume>
<fpage>705</fpage>
<lpage>721</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.104.027920</pub-id>
<pub-id pub-id-type="pmid">15722475</pub-id>
</element-citation>
</ref>
<ref id="CR26"><label>26.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Palatnik</surname>
<given-names>JF</given-names>
</name>
<name><surname>Wollmann</surname>
<given-names>H</given-names>
</name>
<name><surname>Schommer</surname>
<given-names>C</given-names>
</name>
<name><surname>Schwab</surname>
<given-names>R</given-names>
</name>
<name><surname>Boisbouvier</surname>
<given-names>J</given-names>
</name>
<name><surname>Rodriguez</surname>
<given-names>R</given-names>
</name>
<name><surname>Warthmann</surname>
<given-names>N</given-names>
</name>
<name><surname>Allen</surname>
<given-names>E</given-names>
</name>
<name><surname>Dezulian</surname>
<given-names>T</given-names>
</name>
<name><surname>Huson</surname>
<given-names>D</given-names>
</name>
<name><surname>Carrington</surname>
<given-names>JC</given-names>
</name>
<name><surname>Weigel</surname>
<given-names>D</given-names>
</name>
</person-group>
<article-title>Sequence and expression differences underlie functional specialization of <italic>Arabidopsis</italic>
microRNAs miR159 and miR319</article-title>
<source>Dev Cell</source>
<year>2007</year>
<volume>13</volume>
<fpage>115</fpage>
<lpage>125</lpage>
<pub-id pub-id-type="doi">10.1016/j.devcel.2007.04.012</pub-id>
<pub-id pub-id-type="pmid">17609114</pub-id>
</element-citation>
</ref>
<ref id="CR27"><label>27.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Mathieu</surname>
<given-names>J</given-names>
</name>
<name><surname>Yant</surname>
<given-names>LJ</given-names>
</name>
<name><surname>Murdter</surname>
<given-names>F</given-names>
</name>
<name><surname>Kuttner</surname>
<given-names>F</given-names>
</name>
<name><surname>Schmid</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Repression of flowering by the miR172 target SMZ</article-title>
<source>PLoS Biol</source>
<year>2009</year>
<volume>7</volume>
<fpage>e1000148</fpage>
<pub-id pub-id-type="doi">10.1371/journal.pbio.1000148</pub-id>
<pub-id pub-id-type="pmid">19582143</pub-id>
</element-citation>
</ref>
<ref id="CR28"><label>28.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wu</surname>
<given-names>G</given-names>
</name>
<name><surname>Park</surname>
<given-names>MY</given-names>
</name>
<name><surname>Conway</surname>
<given-names>SR</given-names>
</name>
<name><surname>Wang</surname>
<given-names>JW</given-names>
</name>
<name><surname>Weigel</surname>
<given-names>D</given-names>
</name>
<name><surname>Poethig</surname>
<given-names>RS</given-names>
</name>
</person-group>
<article-title>The sequential action of miR156 and miR172 regulates developmental timing in <italic>Arabidopsis</italic>
</article-title>
<source>Cell</source>
<year>2009</year>
<volume>138</volume>
<fpage>750</fpage>
<lpage>759</lpage>
<pub-id pub-id-type="doi">10.1016/j.cell.2009.06.031</pub-id>
<pub-id pub-id-type="pmid">19703400</pub-id>
</element-citation>
</ref>
<ref id="CR29"><label>29.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gandikota</surname>
<given-names>M</given-names>
</name>
<name><surname>Birkenbihl</surname>
<given-names>RP</given-names>
</name>
<name><surname>Hohmann</surname>
<given-names>S</given-names>
</name>
<name><surname>Cardon</surname>
<given-names>GH</given-names>
</name>
<name><surname>Saedler</surname>
<given-names>H</given-names>
</name>
<name><surname>Huijser</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>The miRNA156/157 recognition element in the 3' UTR of the <italic>Arabidopsis</italic>
SBP box gene <italic>SPL3</italic>
prevents early flowering by translational inhibition in seedlings</article-title>
<source>Plant J</source>
<year>2007</year>
<volume>49</volume>
<fpage>683</fpage>
<lpage>693</lpage>
<pub-id pub-id-type="doi">10.1111/j.1365-313X.2006.02983.x</pub-id>
<pub-id pub-id-type="pmid">17217458</pub-id>
</element-citation>
</ref>
<ref id="CR30"><label>30.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname>
<given-names>YC</given-names>
</name>
<name><surname>Yu</surname>
<given-names>Y</given-names>
</name>
<name><surname>Wang</surname>
<given-names>CY</given-names>
</name>
<name><surname>Li</surname>
<given-names>ZY</given-names>
</name>
<name><surname>Liu</surname>
<given-names>Q</given-names>
</name>
<name><surname>Xu</surname>
<given-names>J</given-names>
</name>
<name><surname>Liao</surname>
<given-names>JY</given-names>
</name>
<name><surname>Wang</surname>
<given-names>XJ</given-names>
</name>
<name><surname>Qu</surname>
<given-names>LH</given-names>
</name>
<name><surname>Chen</surname>
<given-names>F</given-names>
</name>
<name><surname>Xin</surname>
<given-names>P</given-names>
</name>
<name><surname>Yan</surname>
<given-names>C</given-names>
</name>
<name><surname>Chu</surname>
<given-names>J</given-names>
</name>
<name><surname>Li</surname>
<given-names>HQ</given-names>
</name>
<name><surname>Chen</surname>
<given-names>YQ</given-names>
</name>
</person-group>
<article-title>Overexpression of microRNA OsmiR397 improves rice yield by increasing grain size and promoting panicle branching</article-title>
<source>Nat Biotechnol</source>
<year>2013</year>
<volume>31</volume>
<fpage>848</fpage>
<lpage>852</lpage>
<pub-id pub-id-type="doi">10.1038/nbt.2646</pub-id>
<pub-id pub-id-type="pmid">23873084</pub-id>
</element-citation>
</ref>
<ref id="CR31"><label>31.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wang</surname>
<given-names>Y</given-names>
</name>
<name><surname>Itaya</surname>
<given-names>A</given-names>
</name>
<name><surname>Zhong</surname>
<given-names>XH</given-names>
</name>
<name><surname>Wu</surname>
<given-names>Y</given-names>
</name>
<name><surname>Zhang</surname>
<given-names>JF</given-names>
</name>
<name><surname>van der Knaap</surname>
<given-names>E</given-names>
</name>
<name><surname>Olmstead</surname>
<given-names>R</given-names>
</name>
<name><surname>Qi</surname>
<given-names>YJ</given-names>
</name>
<name><surname>Ding</surname>
<given-names>BA</given-names>
</name>
</person-group>
<article-title>Function and Evolution of a MicroRNA That Regulates a Ca(2+)-ATPase and Triggers the Formation of Phased Small Interfering RNAs in Tomato Reproductive Growth</article-title>
<source>Plant Cell</source>
<year>2011</year>
<volume>23</volume>
<fpage>3185</fpage>
<lpage>3203</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.111.088013</pub-id>
<pub-id pub-id-type="pmid">21917547</pub-id>
</element-citation>
</ref>
<ref id="CR32"><label>32.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Song</surname>
<given-names>CN</given-names>
</name>
<name><surname>Fang</surname>
<given-names>JG</given-names>
</name>
<name><surname>Li</surname>
<given-names>XY</given-names>
</name>
<name><surname>Liu</surname>
<given-names>H</given-names>
</name>
<name><surname>Chao</surname>
<given-names>CT</given-names>
</name>
</person-group>
<article-title>Identification and characterization of 27 conserved microRNAs in citrus</article-title>
<source>Planta</source>
<year>2009</year>
<volume>230</volume>
<fpage>671</fpage>
<lpage>685</lpage>
<pub-id pub-id-type="doi">10.1007/s00425-009-0971-x</pub-id>
<pub-id pub-id-type="pmid">19585144</pub-id>
</element-citation>
</ref>
<ref id="CR33"><label>33.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Song</surname>
<given-names>CN</given-names>
</name>
<name><surname>Wang</surname>
<given-names>C</given-names>
</name>
<name><surname>Zhang</surname>
<given-names>CQ</given-names>
</name>
<name><surname>Korir</surname>
<given-names>NK</given-names>
</name>
<name><surname>Yu</surname>
<given-names>HP</given-names>
</name>
<name><surname>Ma</surname>
<given-names>ZQ</given-names>
</name>
<name><surname>Fang</surname>
<given-names>JG</given-names>
</name>
</person-group>
<article-title>Deep sequencing discovery of novel and conserved microRNAs in trifoliate orange (<italic>Citrus trifoliata</italic>
)</article-title>
<source>BMC Genomics</source>
<year>2010</year>
<volume>11</volume>
<fpage>431</fpage>
<pub-id pub-id-type="doi">10.1186/1471-2164-11-431</pub-id>
<pub-id pub-id-type="pmid">20626894</pub-id>
</element-citation>
</ref>
<ref id="CR34"><label>34.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname>
<given-names>JZ</given-names>
</name>
<name><surname>Ai</surname>
<given-names>XY</given-names>
</name>
<name><surname>Guo</surname>
<given-names>WW</given-names>
</name>
<name><surname>Peng</surname>
<given-names>SA</given-names>
</name>
<name><surname>Deng</surname>
<given-names>XX</given-names>
</name>
<name><surname>Hu</surname>
<given-names>CG</given-names>
</name>
</person-group>
<article-title>Identification of miRNAs and Their Target Genes Using Deep Sequencing and Degradome Analysis in Trifoliate Orange <italic>Poncirus trifoliate</italic>
(L.) Raf</article-title>
<source>Mol Biotechnol</source>
<year>2012</year>
<volume>51</volume>
<fpage>44</fpage>
<lpage>57</lpage>
<pub-id pub-id-type="doi">10.1007/s12033-011-9439-x</pub-id>
<pub-id pub-id-type="pmid">21796478</pub-id>
</element-citation>
</ref>
<ref id="CR35"><label>35.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Xu</surname>
<given-names>Q</given-names>
</name>
<name><surname>Liu</surname>
<given-names>YL</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>AD</given-names>
</name>
<name><surname>Wu</surname>
<given-names>XM</given-names>
</name>
<name><surname>Ye</surname>
<given-names>JL</given-names>
</name>
<name><surname>Yu</surname>
<given-names>KQ</given-names>
</name>
<name><surname>Guo</surname>
<given-names>WW</given-names>
</name>
<name><surname>Deng</surname>
<given-names>XX</given-names>
</name>
</person-group>
<article-title>Discovery and comparative profiling of microRNAs in a sweet orange red-flesh mutant and its wild type</article-title>
<source>BMC Genomics</source>
<year>2010</year>
<volume>11</volume>
<fpage>246</fpage>
<pub-id pub-id-type="doi">10.1186/1471-2164-11-246</pub-id>
<pub-id pub-id-type="pmid">20398412</pub-id>
</element-citation>
</ref>
<ref id="CR36"><label>36.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Xu</surname>
<given-names>Q</given-names>
</name>
<name><surname>Chen</surname>
<given-names>LL</given-names>
</name>
<name><surname>Ruan</surname>
<given-names>XA</given-names>
</name>
<name><surname>Chen</surname>
<given-names>DJ</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>AD</given-names>
</name>
<name><surname>Chen</surname>
<given-names>CL</given-names>
</name>
<name><surname>Bertrand</surname>
<given-names>D</given-names>
</name>
<name><surname>Jiao</surname>
<given-names>WB</given-names>
</name>
<name><surname>Hao</surname>
<given-names>BH</given-names>
</name>
<name><surname>Lyon</surname>
<given-names>MP</given-names>
</name>
<name><surname>Chen</surname>
<given-names>J</given-names>
</name>
<name><surname>Gao</surname>
<given-names>S</given-names>
</name>
<name><surname>Xing</surname>
<given-names>F</given-names>
</name>
<name><surname>Lan</surname>
<given-names>H</given-names>
</name>
<name><surname>Chang</surname>
<given-names>JW</given-names>
</name>
<name><surname>Ge</surname>
<given-names>X</given-names>
</name>
<name><surname>Lei</surname>
<given-names>Y</given-names>
</name>
<name><surname>Hu</surname>
<given-names>Q</given-names>
</name>
<name><surname>Miao</surname>
<given-names>Y</given-names>
</name>
<name><surname>Wang</surname>
<given-names>L</given-names>
</name>
<name><surname>Xiao</surname>
<given-names>S</given-names>
</name>
<name><surname>Biswas</surname>
<given-names>MK</given-names>
</name>
<name><surname>Zeng</surname>
<given-names>W</given-names>
</name>
<name><surname>Guo</surname>
<given-names>F</given-names>
</name>
<name><surname>Cao</surname>
<given-names>H</given-names>
</name>
<name><surname>Yang</surname>
<given-names>X</given-names>
</name>
<name><surname>Xu</surname>
<given-names>XW</given-names>
</name>
<name><surname>Cheng</surname>
<given-names>YJ</given-names>
</name>
<name><surname>Xu</surname>
<given-names>J</given-names>
</name>
<name><surname>Liu</surname>
<given-names>JH</given-names>
</name>
<etal></etal>
</person-group>
<article-title>The draft genome of sweet orange (<italic>Citrus sinensis</italic>
)</article-title>
<source>Nat Genet</source>
<year>2013</year>
<volume>45</volume>
<fpage>59</fpage>
<lpage>66</lpage>
<pub-id pub-id-type="doi">10.1038/ng.2472</pub-id>
<pub-id pub-id-type="pmid">23179022</pub-id>
</element-citation>
</ref>
<ref id="CR37"><label>37.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Rajagopalan</surname>
<given-names>R</given-names>
</name>
<name><surname>Vaucheret</surname>
<given-names>H</given-names>
</name>
<name><surname>Trejo</surname>
<given-names>J</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>A diverse and evolutionarily fluid set of microRNAs in <italic>Arabidopsis thaliana</italic>
</article-title>
<source>Genes Dev</source>
<year>2006</year>
<volume>20</volume>
<fpage>3407</fpage>
<lpage>3425</lpage>
<pub-id pub-id-type="doi">10.1101/gad.1476406</pub-id>
<pub-id pub-id-type="pmid">17182867</pub-id>
</element-citation>
</ref>
<ref id="CR38"><label>38.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Moxon</surname>
<given-names>S</given-names>
</name>
<name><surname>Jing</surname>
<given-names>RC</given-names>
</name>
<name><surname>Szittya</surname>
<given-names>G</given-names>
</name>
<name><surname>Schwach</surname>
<given-names>F</given-names>
</name>
<name><surname>Pilcher</surname>
<given-names>RLR</given-names>
</name>
<name><surname>Moulton</surname>
<given-names>V</given-names>
</name>
<name><surname>Dalmay</surname>
<given-names>T</given-names>
</name>
</person-group>
<article-title>Deep sequencing of tomato short RNAs identifies microRNAs targeting genes involved in fruit ripening</article-title>
<source>Genome Res</source>
<year>2008</year>
<volume>18</volume>
<fpage>1602</fpage>
<lpage>1609</lpage>
<pub-id pub-id-type="doi">10.1101/gr.080127.108</pub-id>
<pub-id pub-id-type="pmid">18653800</pub-id>
</element-citation>
</ref>
<ref id="CR39"><label>39.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Addo-Quaye</surname>
<given-names>C</given-names>
</name>
<name><surname>Eshoo</surname>
<given-names>TW</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
<name><surname>Axtell</surname>
<given-names>MJ</given-names>
</name>
</person-group>
<article-title>Endogenous siRNA and miRNA targets identified by sequencing of the <italic>Arabidopsis</italic>
degradome</article-title>
<source>Curr Biol</source>
<year>2008</year>
<volume>18</volume>
<fpage>758</fpage>
<lpage>762</lpage>
<pub-id pub-id-type="doi">10.1016/j.cub.2008.04.042</pub-id>
<pub-id pub-id-type="pmid">18472421</pub-id>
</element-citation>
</ref>
<ref id="CR40"><label>40.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Vaucheret</surname>
<given-names>H</given-names>
</name>
<name><surname>Vazquez</surname>
<given-names>F</given-names>
</name>
<name><surname>Crete</surname>
<given-names>P</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>The action of <italic>ARGONAUTE1</italic>
in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development</article-title>
<source>Genes Dev</source>
<year>2004</year>
<volume>18</volume>
<fpage>1187</fpage>
<lpage>1197</lpage>
<pub-id pub-id-type="doi">10.1101/gad.1201404</pub-id>
<pub-id pub-id-type="pmid">15131082</pub-id>
</element-citation>
</ref>
<ref id="CR41"><label>41.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Vaucheret</surname>
<given-names>H</given-names>
</name>
<name><surname>Mallory</surname>
<given-names>AC</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
</person-group>
<article-title>AGO1 homeostasis entails coexpression of <italic>MIR168</italic>
and <italic>AGO1</italic>
and preferential stabilization of miR168 by AGO1</article-title>
<source>Mol Cell</source>
<year>2006</year>
<volume>22</volume>
<fpage>129</fpage>
<lpage>136</lpage>
<pub-id pub-id-type="doi">10.1016/j.molcel.2006.03.011</pub-id>
<pub-id pub-id-type="pmid">16600876</pub-id>
</element-citation>
</ref>
<ref id="CR42"><label>42.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Allen</surname>
<given-names>RS</given-names>
</name>
<name><surname>Li</surname>
<given-names>J</given-names>
</name>
<name><surname>Stahle</surname>
<given-names>MI</given-names>
</name>
<name><surname>Dubroue</surname>
<given-names>A</given-names>
</name>
<name><surname>Gubler</surname>
<given-names>F</given-names>
</name>
<name><surname>Millar</surname>
<given-names>AA</given-names>
</name>
</person-group>
<article-title>Genetic analysis reveals functional redundancy and the major target genes of the <italic>Arabidopsis</italic>
miR159 family</article-title>
<source>Proc Natl Acad Sci U S A</source>
<year>2007</year>
<volume>104</volume>
<fpage>16371</fpage>
<lpage>16376</lpage>
<pub-id pub-id-type="doi">10.1073/pnas.0707653104</pub-id>
<pub-id pub-id-type="pmid">17916625</pub-id>
</element-citation>
</ref>
<ref id="CR43"><label>43.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Reyes</surname>
<given-names>JL</given-names>
</name>
<name><surname>Chua</surname>
<given-names>NH</given-names>
</name>
</person-group>
<article-title>ABA induction of miR159 controls transcript levels of two MYB factors during <italic>Arabidopsis</italic>
seed germination</article-title>
<source>Plant J</source>
<year>2007</year>
<volume>49</volume>
<fpage>592</fpage>
<lpage>606</lpage>
<pub-id pub-id-type="doi">10.1111/j.1365-313X.2006.02980.x</pub-id>
<pub-id pub-id-type="pmid">17217461</pub-id>
</element-citation>
</ref>
<ref id="CR44"><label>44.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Jeong</surname>
<given-names>DH</given-names>
</name>
<name><surname>Park</surname>
<given-names>S</given-names>
</name>
<name><surname>Zhai</surname>
<given-names>J</given-names>
</name>
<name><surname>Gurazada</surname>
<given-names>SG</given-names>
</name>
<name><surname>De Paoli</surname>
<given-names>E</given-names>
</name>
<name><surname>Meyers</surname>
<given-names>BC</given-names>
</name>
<name><surname>Green</surname>
<given-names>PJ</given-names>
</name>
</person-group>
<article-title>Massive analysis of rice small RNAs: mechanistic implications of regulated microRNAs and variants for differential target RNA cleavage</article-title>
<source>Plant Cell</source>
<year>2011</year>
<volume>23</volume>
<fpage>4185</fpage>
<lpage>4207</lpage>
<pub-id pub-id-type="doi">10.1105/tpc.111.089045</pub-id>
<pub-id pub-id-type="pmid">22158467</pub-id>
</element-citation>
</ref>
<ref id="CR45"><label>45.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Allen</surname>
<given-names>E</given-names>
</name>
<name><surname>Xie</surname>
<given-names>Z</given-names>
</name>
<name><surname>Gustafson</surname>
<given-names>AM</given-names>
</name>
<name><surname>Carrington</surname>
<given-names>JC</given-names>
</name>
</person-group>
<article-title>microRNA-directed phasing during trans-acting siRNA biogenesis in plants</article-title>
<source>Cell</source>
<year>2005</year>
<volume>121</volume>
<fpage>207</fpage>
<lpage>221</lpage>
<pub-id pub-id-type="doi">10.1016/j.cell.2005.04.004</pub-id>
<pub-id pub-id-type="pmid">15851028</pub-id>
</element-citation>
</ref>
<ref id="CR46"><label>46.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Xia</surname>
<given-names>R</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>H</given-names>
</name>
<name><surname>An</surname>
<given-names>Y</given-names>
</name>
<name><surname>Beers</surname>
<given-names>EP</given-names>
</name>
<name><surname>Liu</surname>
<given-names>Z</given-names>
</name>
</person-group>
<article-title>Apple miRNAs and tasiRNAs with novel regulatory networks</article-title>
<source>Genome Biol</source>
<year>2012</year>
<volume>13</volume>
<fpage>R47</fpage>
<pub-id pub-id-type="doi">10.1186/gb-2012-13-6-r47</pub-id>
<pub-id pub-id-type="pmid">22704043</pub-id>
</element-citation>
</ref>
<ref id="CR47"><label>47.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Tang</surname>
<given-names>S</given-names>
</name>
<name><surname>Wang</surname>
<given-names>Y</given-names>
</name>
<name><surname>Li</surname>
<given-names>Z</given-names>
</name>
<name><surname>Gui</surname>
<given-names>Y</given-names>
</name>
<name><surname>Xiao</surname>
<given-names>B</given-names>
</name>
<name><surname>Xie</surname>
<given-names>J</given-names>
</name>
<name><surname>Zhu</surname>
<given-names>QH</given-names>
</name>
<name><surname>Fan</surname>
<given-names>L</given-names>
</name>
</person-group>
<article-title>Identification of wounding and topping responsive small RNAs in tobacco (<italic>Nicotiana tabacum</italic>
)</article-title>
<source>BMC Plant Biol</source>
<year>2012</year>
<volume>12</volume>
<fpage>28</fpage>
<pub-id pub-id-type="doi">10.1186/1471-2229-12-28</pub-id>
<pub-id pub-id-type="pmid">22353177</pub-id>
</element-citation>
</ref>
<ref id="CR48"><label>48.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Li</surname>
<given-names>F</given-names>
</name>
<name><surname>Pignatta</surname>
<given-names>D</given-names>
</name>
<name><surname>Bendix</surname>
<given-names>C</given-names>
</name>
<name><surname>Brunkard</surname>
<given-names>JO</given-names>
</name>
<name><surname>Cohn</surname>
<given-names>MM</given-names>
</name>
<name><surname>Tung</surname>
<given-names>J</given-names>
</name>
<name><surname>Sun</surname>
<given-names>H</given-names>
</name>
<name><surname>Kumar</surname>
<given-names>P</given-names>
</name>
<name><surname>Baker</surname>
<given-names>B</given-names>
</name>
</person-group>
<article-title>MicroRNA regulation of plant innate immune receptors</article-title>
<source>Proc Natl Acad Sci U S A</source>
<year>2012</year>
<volume>109</volume>
<fpage>1790</fpage>
<lpage>1795</lpage>
<pub-id pub-id-type="doi">10.1073/pnas.1118282109</pub-id>
<pub-id pub-id-type="pmid">22307647</pub-id>
</element-citation>
</ref>
<ref id="CR49"><label>49.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chen</surname>
<given-names>M</given-names>
</name>
<name><surname>Tan</surname>
<given-names>ZY</given-names>
</name>
<name><surname>Zeng</surname>
<given-names>GM</given-names>
</name>
<name><surname>Peng</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Comprehensive Analysis of Simple Sequence Repeats in Pre-miRNAs</article-title>
<source>Mol Biol Evol</source>
<year>2010</year>
<volume>27</volume>
<fpage>2227</fpage>
<lpage>2232</lpage>
<pub-id pub-id-type="doi">10.1093/molbev/msq100</pub-id>
<pub-id pub-id-type="pmid">20395311</pub-id>
</element-citation>
</ref>
<ref id="CR50"><label>50.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Li</surname>
<given-names>YC</given-names>
</name>
<name><surname>Korol</surname>
<given-names>AB</given-names>
</name>
<name><surname>Fahima</surname>
<given-names>T</given-names>
</name>
<name><surname>Beiles</surname>
<given-names>A</given-names>
</name>
<name><surname>Nevo</surname>
<given-names>E</given-names>
</name>
</person-group>
<article-title>Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review</article-title>
<source>Mol Ecol</source>
<year>2002</year>
<volume>11</volume>
<fpage>2453</fpage>
<lpage>2465</lpage>
<pub-id pub-id-type="doi">10.1046/j.1365-294X.2002.01643.x</pub-id>
<pub-id pub-id-type="pmid">12453231</pub-id>
</element-citation>
</ref>
<ref id="CR51"><label>51.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname>
<given-names>L</given-names>
</name>
<name><surname>Chia</surname>
<given-names>J-M</given-names>
</name>
<name><surname>Kumari</surname>
<given-names>S</given-names>
</name>
<name><surname>Stein</surname>
<given-names>JC</given-names>
</name>
<name><surname>Liu</surname>
<given-names>Z</given-names>
</name>
<name><surname>Narechania</surname>
<given-names>A</given-names>
</name>
<name><surname>Maher</surname>
<given-names>CA</given-names>
</name>
<name><surname>Guill</surname>
<given-names>K</given-names>
</name>
<name><surname>McMullen</surname>
<given-names>MD</given-names>
</name>
<name><surname>Ware</surname>
<given-names>D</given-names>
</name>
</person-group>
<article-title>A genome-wide characterization of microRNA genes in maize</article-title>
<source>PLoS Genet</source>
<year>2009</year>
<volume>5</volume>
<fpage>e1000716</fpage>
<pub-id pub-id-type="doi">10.1371/journal.pgen.1000716</pub-id>
<pub-id pub-id-type="pmid">19936050</pub-id>
</element-citation>
</ref>
<ref id="CR52"><label>52.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Pantaleo</surname>
<given-names>V</given-names>
</name>
<name><surname>Szittya</surname>
<given-names>G</given-names>
</name>
<name><surname>Moxon</surname>
<given-names>S</given-names>
</name>
<name><surname>Miozzi</surname>
<given-names>L</given-names>
</name>
<name><surname>Moulton</surname>
<given-names>V</given-names>
</name>
<name><surname>Dalmay</surname>
<given-names>T</given-names>
</name>
<name><surname>Burgyan</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Identification of grapevine microRNAs and their targets using high-throughput sequencing and degradome analysis</article-title>
<source>Plant J</source>
<year>2010</year>
<volume>62</volume>
<fpage>960</fpage>
<lpage>976</lpage>
<pub-id pub-id-type="pmid">20230504</pub-id>
</element-citation>
</ref>
<ref id="CR53"><label>53.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Takada</surname>
<given-names>S</given-names>
</name>
<name><surname>Hibara</surname>
<given-names>K-i</given-names>
</name>
<name><surname>Ishida</surname>
<given-names>T</given-names>
</name>
<name><surname>Tasaka</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>The CUP-SHAPED COTYLEDON1 gene of Arabidopsis regulates shoot apical meristem formation</article-title>
<source>Development</source>
<year>2001</year>
<volume>128</volume>
<fpage>1127</fpage>
<lpage>1135</lpage>
<pub-id pub-id-type="pmid">11245578</pub-id>
</element-citation>
</ref>
<ref id="CR54"><label>54.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Mallory</surname>
<given-names>AC</given-names>
</name>
<name><surname>Dugas</surname>
<given-names>DV</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>DP</given-names>
</name>
<name><surname>Bartel</surname>
<given-names>B</given-names>
</name>
</person-group>
<article-title>MicroRNA regulation of NAC-domain targets is required for proper formation and separation of adjacent embryonic, vegetative, and floral organs</article-title>
<source>Curr Biol</source>
<year>2004</year>
<volume>14</volume>
<fpage>1035</fpage>
<lpage>1046</lpage>
<pub-id pub-id-type="doi">10.1016/j.cub.2004.06.022</pub-id>
<pub-id pub-id-type="pmid">15202996</pub-id>
</element-citation>
</ref>
<ref id="CR55"><label>55.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Guo</surname>
<given-names>Y</given-names>
</name>
<name><surname>Gan</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title><italic>AtNAP</italic>
, a NAC family transcription factor, has an important role in leaf senescence</article-title>
<source>Plant J</source>
<year>2006</year>
<volume>46</volume>
<fpage>601</fpage>
<lpage>612</lpage>
<pub-id pub-id-type="doi">10.1111/j.1365-313X.2006.02723.x</pub-id>
<pub-id pub-id-type="pmid">16640597</pub-id>
</element-citation>
</ref>
<ref id="CR56"><label>56.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Nakashima</surname>
<given-names>K</given-names>
</name>
<name><surname>Tran</surname>
<given-names>LSP</given-names>
</name>
<name><surname>Van Nguyen</surname>
<given-names>D</given-names>
</name>
<name><surname>Fujita</surname>
<given-names>M</given-names>
</name>
<name><surname>Maruyama</surname>
<given-names>K</given-names>
</name>
<name><surname>Todaka</surname>
<given-names>D</given-names>
</name>
<name><surname>Ito</surname>
<given-names>Y</given-names>
</name>
<name><surname>Hayashi</surname>
<given-names>N</given-names>
</name>
<name><surname>Shinozaki</surname>
<given-names>K</given-names>
</name>
<name><surname>Yamaguchi-Shinozaki</surname>
<given-names>K</given-names>
</name>
</person-group>
<article-title>Functional analysis of a NAC-type transcription factor <italic>OsNAC6</italic>
involved in abiotic and biotic stress-responsive gene expression in rice</article-title>
<source>Plant J</source>
<year>2007</year>
<volume>51</volume>
<fpage>617</fpage>
<lpage>630</lpage>
<pub-id pub-id-type="doi">10.1111/j.1365-313X.2007.03168.x</pub-id>
<pub-id pub-id-type="pmid">17587305</pub-id>
</element-citation>
</ref>
<ref id="CR57"><label>57.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shan</surname>
<given-names>W</given-names>
</name>
<name><surname>Kuang</surname>
<given-names>J-f</given-names>
</name>
<name><surname>Chen</surname>
<given-names>L</given-names>
</name>
<name><surname>Xie</surname>
<given-names>H</given-names>
</name>
<name><surname>Peng</surname>
<given-names>H-h</given-names>
</name>
<name><surname>Xiao</surname>
<given-names>Y-y</given-names>
</name>
<name><surname>Li</surname>
<given-names>X-p</given-names>
</name>
<name><surname>Chen</surname>
<given-names>W-x</given-names>
</name>
<name><surname>He</surname>
<given-names>Q-g</given-names>
</name>
<name><surname>Chen</surname>
<given-names>J-y</given-names>
</name>
<name><surname>Lu</surname>
<given-names>W-j</given-names>
</name>
</person-group>
<article-title>Molecular characterization of banana NAC transcription factors and their interactions with ethylene signalling component EIL during fruit ripening</article-title>
<source>J Exp Bot</source>
<year>2012</year>
<volume>63</volume>
<fpage>5171</fpage>
<lpage>5187</lpage>
<pub-id pub-id-type="doi">10.1093/jxb/ers178</pub-id>
<pub-id pub-id-type="pmid">22888129</pub-id>
</element-citation>
</ref>
<ref id="CR58"><label>58.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Fan</surname>
<given-names>J</given-names>
</name>
<name><surname>Gao</surname>
<given-names>X</given-names>
</name>
<name><surname>Yang</surname>
<given-names>Y-W</given-names>
</name>
<name><surname>Deng</surname>
<given-names>W</given-names>
</name>
<name><surname>Li</surname>
<given-names>Z-G</given-names>
</name>
</person-group>
<article-title>Molecular cloning and characterization of a NAC-like gene in “navel” orange fruit response to postharvest stresses</article-title>
<source>Plant Mol Biol Rep</source>
<year>2007</year>
<volume>25</volume>
<fpage>145</fpage>
<lpage>153</lpage>
<pub-id pub-id-type="doi">10.1007/s11105-007-0016-1</pub-id>
</element-citation>
</ref>
<ref id="CR59"><label>59.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liu</surname>
<given-names>Y-Z</given-names>
</name>
<name><surname>Baig</surname>
<given-names>M</given-names>
</name>
<name><surname>Fan</surname>
<given-names>R</given-names>
</name>
<name><surname>Ye</surname>
<given-names>J-L</given-names>
</name>
<name><surname>Cao</surname>
<given-names>Y-C</given-names>
</name>
<name><surname>Deng</surname>
<given-names>X-X</given-names>
</name>
</person-group>
<article-title>Identification and expression pattern of a novel NAM, ATAF, and CUC-like gene from Citrus sinensis Osbeck</article-title>
<source>Plant Mol Biol Rep</source>
<year>2009</year>
<volume>27</volume>
<fpage>292</fpage>
<lpage>297</lpage>
<pub-id pub-id-type="doi">10.1007/s11105-008-0082-z</pub-id>
</element-citation>
</ref>
<ref id="CR60"><label>60.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chen</surname>
<given-names>CF</given-names>
</name>
<name><surname>Ridzon</surname>
<given-names>DA</given-names>
</name>
<name><surname>Broomer</surname>
<given-names>AJ</given-names>
</name>
<name><surname>Zhou</surname>
<given-names>ZH</given-names>
</name>
<name><surname>Lee</surname>
<given-names>DH</given-names>
</name>
<name><surname>Nguyen</surname>
<given-names>JT</given-names>
</name>
<name><surname>Barbisin</surname>
<given-names>M</given-names>
</name>
<name><surname>Xu</surname>
<given-names>NL</given-names>
</name>
<name><surname>Mahuvakar</surname>
<given-names>VR</given-names>
</name>
<name><surname>Andersen</surname>
<given-names>MR</given-names>
</name>
<name><surname>Lao</surname>
<given-names>KQ</given-names>
</name>
<name><surname>Livak</surname>
<given-names>KJ</given-names>
</name>
<name><surname>Guegler</surname>
<given-names>KJ</given-names>
</name>
</person-group>
<article-title>Real-time quantification of microRNAs by stem-loop RT-PCR</article-title>
<source>Nucleic Acids Res</source>
<year>2005</year>
<volume>33</volume>
<fpage>e179</fpage>
<pub-id pub-id-type="doi">10.1093/nar/gni178</pub-id>
<pub-id pub-id-type="pmid">16314309</pub-id>
</element-citation>
</ref>
<ref id="CR61"><label>61.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Varkonyi-Gasic</surname>
<given-names>E</given-names>
</name>
<name><surname>Wu</surname>
<given-names>RM</given-names>
</name>
<name><surname>Wood</surname>
<given-names>M</given-names>
</name>
<name><surname>Walton</surname>
<given-names>EF</given-names>
</name>
<name><surname>Hellens</surname>
<given-names>RP</given-names>
</name>
</person-group>
<article-title>Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs</article-title>
<source>Plant Methods</source>
<year>2007</year>
<volume>3</volume>
<fpage>12</fpage>
<pub-id pub-id-type="doi">10.1186/1746-4811-3-12</pub-id>
<pub-id pub-id-type="pmid">17931426</pub-id>
</element-citation>
</ref>
<ref id="CR62"><label>62.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kou</surname>
<given-names>SJ</given-names>
</name>
<name><surname>Wu</surname>
<given-names>XM</given-names>
</name>
<name><surname>Liu</surname>
<given-names>Z</given-names>
</name>
<name><surname>Liu</surname>
<given-names>YL</given-names>
</name>
<name><surname>Xu</surname>
<given-names>Q</given-names>
</name>
<name><surname>Guo</surname>
<given-names>WW</given-names>
</name>
</person-group>
<article-title>Selection and validation of suitable reference genes for miRNA expression normalization by quantitative RT-PCR in citrus somatic embryogenic and adult tissues</article-title>
<source>Plant Cell Rep</source>
<year>2012</year>
<volume>31</volume>
<fpage>2151</fpage>
<lpage>2163</lpage>
<pub-id pub-id-type="doi">10.1007/s00299-012-1325-x</pub-id>
<pub-id pub-id-type="pmid">22865195</pub-id>
</element-citation>
</ref>
<ref id="CR63"><label>63.</label>
<element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Sparkes</surname>
<given-names>IA</given-names>
</name>
<name><surname>Runions</surname>
<given-names>J</given-names>
</name>
<name><surname>Kearns</surname>
<given-names>A</given-names>
</name>
<name><surname>Hawes</surname>
<given-names>C</given-names>
</name>
</person-group>
<article-title>Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants</article-title>
<source>Nat Protoc</source>
<year>2006</year>
<volume>1</volume>
<fpage>2019</fpage>
<lpage>2025</lpage>
<pub-id pub-id-type="doi">10.1038/nprot.2006.286</pub-id>
<pub-id pub-id-type="pmid">17487191</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</pmc>
</record>
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