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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Cloning and Expression Profiling of the Polycomb Gene, <italic>Retinoblastoma-related</italic>
Protein from Tomato <italic>Solanum lycopersicum</italic>
L.</title>
<author><name sortKey="Almutairi, Zainab M" sort="Almutairi, Zainab M" uniqKey="Almutairi Z" first="Zainab M" last="Almutairi">Zainab M. Almutairi</name>
<affiliation><nlm:aff id="af1-ebo-10-2014-177">Department of Biology, College of Science and Humanities, Salman bin Abdulaziz University, Al-Kharj, Saudi Arabia.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sadder, Monther T" sort="Sadder, Monther T" uniqKey="Sadder M" first="Monther T" last="Sadder">Monther T. Sadder</name>
<affiliation><nlm:aff id="af2-ebo-10-2014-177">Center of Excellence in Biotechnology Research, King Saud University, Riyadh, Saudi Arabia.</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af3-ebo-10-2014-177">Plant Biotechnology Lab, Faculty of Agriculture, The University of Jordan, Amman, Jordan.</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">25374451</idno>
<idno type="pmc">4213193</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213193</idno>
<idno type="RBID">PMC:4213193</idno>
<idno type="doi">10.4137/EBO.S16932</idno>
<date when="2014">2014</date>
<idno type="wicri:Area/Pmc/Corpus">000F05</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Cloning and Expression Profiling of the Polycomb Gene, <italic>Retinoblastoma-related</italic>
Protein from Tomato <italic>Solanum lycopersicum</italic>
L.</title>
<author><name sortKey="Almutairi, Zainab M" sort="Almutairi, Zainab M" uniqKey="Almutairi Z" first="Zainab M" last="Almutairi">Zainab M. Almutairi</name>
<affiliation><nlm:aff id="af1-ebo-10-2014-177">Department of Biology, College of Science and Humanities, Salman bin Abdulaziz University, Al-Kharj, Saudi Arabia.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sadder, Monther T" sort="Sadder, Monther T" uniqKey="Sadder M" first="Monther T" last="Sadder">Monther T. Sadder</name>
<affiliation><nlm:aff id="af2-ebo-10-2014-177">Center of Excellence in Biotechnology Research, King Saud University, Riyadh, Saudi Arabia.</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af3-ebo-10-2014-177">Plant Biotechnology Lab, Faculty of Agriculture, The University of Jordan, Amman, Jordan.</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">Evolutionary Bioinformatics Online</title>
<idno type="eISSN">1176-9343</idno>
<imprint><date when="2014">2014</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Cell cycle regulation mechanisms appear to be conserved throughout eukaryotic evolution. One of the important proteins involved in the regulation of cell cycle processes is retinoblastoma-related protein (RBR), which is a negative regulator of cell cycle progression, controlling the G1/S transition in plants and animals. In this study, we present the cloning and genomic structure of a putative <italic>SlRBR</italic>
gene in the tomato <italic>Solanum lycopersicum</italic>
L. by isolating cDNA clones that correspond to the <italic>SlRBR</italic>
gene from tomato using primers that were designed from available Solanaceae ESTs based on conserved sequences between the PcG genes in <italic>Arabidopsis thaliana</italic>
and tomato. The <italic>SlRBR</italic>
cDNAs were cloned into the pBS plasmid and sequenced. Both 5′- and 3′-RACE were generated and sequenced. FlcDNA of the <italic>SlRBR</italic>
gene of 3,554 bp was composed of a 5′-UTR of 140 bp, an ORF of 3,054 bp, and a 3′-UTR of 360 bp. The translated ORF encodes a polypeptide of 1,018 amino acids. An alignment of the deduced amino acids indicates that there are highly conserved regions between the tomato SlRBR predicted protein and plant hypothetical <italic>RBR</italic>
gene family members. Both of the unrooted phylogenetic trees, which were constructed using maximum parsimony and maximum likelihood methods, indicate a close relationship between the SlRBR predicted protein and the RBR protein of <italic>Nicotiana benthamiana</italic>
. QRT-PCR indicates that <italic>SlRBR</italic>
gene is expressed in closed floral bud tissues 1.7 times higher than in flower tissues, whereas the expression level in unripe fruit tissue is lower by about three times than in flower tissues.</p>
</div>
</front>
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<biblStruct><analytic><author><name sortKey="Marchler Bauer, A" uniqKey="Marchler Bauer A">A Marchler-Bauer</name>
</author>
<author><name sortKey="Bryant, Sh" uniqKey="Bryant S">SH Bryant</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Marchler Bauer, A" uniqKey="Marchler Bauer A">A Marchler-Bauer</name>
</author>
<author><name sortKey="Anderson, Jb" uniqKey="Anderson J">JB Anderson</name>
</author>
<author><name sortKey="Chitsaz, F" uniqKey="Chitsaz F">F Chitsaz</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Marchler Bauer, A" uniqKey="Marchler Bauer A">A Marchler-Bauer</name>
</author>
<author><name sortKey="Lu, S" uniqKey="Lu S">S Lu</name>
</author>
<author><name sortKey="Anderson, Jb" uniqKey="Anderson J">JB Anderson</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Livak, Kj" uniqKey="Livak K">KJ Livak</name>
</author>
<author><name sortKey="Schmittgen, Td" uniqKey="Schmittgen T">TD Schmittgen</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">Evol Bioinform Online</journal-id>
<journal-id journal-id-type="iso-abbrev">Evol. Bioinform. Online</journal-id>
<journal-id journal-id-type="publisher-id">Evolutionary Bioinformatics</journal-id>
<journal-title-group><journal-title>Evolutionary Bioinformatics Online</journal-title>
</journal-title-group>
<issn pub-type="epub">1176-9343</issn>
<publisher><publisher-name>Libertas Academica</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25374451</article-id>
<article-id pub-id-type="pmc">4213193</article-id>
<article-id pub-id-type="doi">10.4137/EBO.S16932</article-id>
<article-id pub-id-type="publisher-id">ebo-10-2014-177</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Original Research</subject>
</subj-group>
</article-categories>
<title-group><article-title>Cloning and Expression Profiling of the Polycomb Gene, <italic>Retinoblastoma-related</italic>
Protein from Tomato <italic>Solanum lycopersicum</italic>
L.</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Almutairi</surname>
<given-names>Zainab M</given-names>
</name>
<xref ref-type="aff" rid="af1-ebo-10-2014-177">1</xref>
<xref ref-type="corresp" rid="c1-ebo-10-2014-177"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sadder</surname>
<given-names>Monther T</given-names>
</name>
<xref ref-type="aff" rid="af2-ebo-10-2014-177">2</xref>
<xref ref-type="aff" rid="af3-ebo-10-2014-177">3</xref>
</contrib>
</contrib-group>
<aff id="af1-ebo-10-2014-177"><label>1</label>
Department of Biology, College of Science and Humanities, Salman bin Abdulaziz University, Al-Kharj, Saudi Arabia.</aff>
<aff id="af2-ebo-10-2014-177"><label>2</label>
Center of Excellence in Biotechnology Research, King Saud University, Riyadh, Saudi Arabia.</aff>
<aff id="af3-ebo-10-2014-177"><label>3</label>
Plant Biotechnology Lab, Faculty of Agriculture, The University of Jordan, Amman, Jordan.</aff>
<author-notes><corresp id="c1-ebo-10-2014-177">CORRESPONDENCE: <email>z.almutairi@sau.edu.sa</email>
</corresp>
</author-notes>
<pub-date pub-type="collection"><year>2014</year>
</pub-date>
<pub-date pub-type="epub"><day>23</day>
<month>10</month>
<year>2014</year>
</pub-date>
<volume>10</volume>
<fpage>177</fpage>
<lpage>185</lpage>
<history><date date-type="received"><day>14</day>
<month>5</month>
<year>2014</year>
</date>
<date date-type="rev-recd"><day>05</day>
<month>7</month>
<year>2014</year>
</date>
<date date-type="accepted"><day>10</day>
<month>7</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>© 2014 the author(s), publisher and licensee Libertas Academica Ltd.</copyright-statement>
<copyright-year>2014</copyright-year>
<license license-type="open-access"><license-p>This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.</license-p>
</license>
</permissions>
<abstract><p>Cell cycle regulation mechanisms appear to be conserved throughout eukaryotic evolution. One of the important proteins involved in the regulation of cell cycle processes is retinoblastoma-related protein (RBR), which is a negative regulator of cell cycle progression, controlling the G1/S transition in plants and animals. In this study, we present the cloning and genomic structure of a putative <italic>SlRBR</italic>
gene in the tomato <italic>Solanum lycopersicum</italic>
L. by isolating cDNA clones that correspond to the <italic>SlRBR</italic>
gene from tomato using primers that were designed from available Solanaceae ESTs based on conserved sequences between the PcG genes in <italic>Arabidopsis thaliana</italic>
and tomato. The <italic>SlRBR</italic>
cDNAs were cloned into the pBS plasmid and sequenced. Both 5′- and 3′-RACE were generated and sequenced. FlcDNA of the <italic>SlRBR</italic>
gene of 3,554 bp was composed of a 5′-UTR of 140 bp, an ORF of 3,054 bp, and a 3′-UTR of 360 bp. The translated ORF encodes a polypeptide of 1,018 amino acids. An alignment of the deduced amino acids indicates that there are highly conserved regions between the tomato SlRBR predicted protein and plant hypothetical <italic>RBR</italic>
gene family members. Both of the unrooted phylogenetic trees, which were constructed using maximum parsimony and maximum likelihood methods, indicate a close relationship between the SlRBR predicted protein and the RBR protein of <italic>Nicotiana benthamiana</italic>
. QRT-PCR indicates that <italic>SlRBR</italic>
gene is expressed in closed floral bud tissues 1.7 times higher than in flower tissues, whereas the expression level in unripe fruit tissue is lower by about three times than in flower tissues.</p>
</abstract>
<kwd-group><kwd>tomato</kwd>
<kwd>retinoblastoma-related gene</kwd>
<kwd>FlcDNA</kwd>
<kwd>phylogenetics</kwd>
</kwd-group>
</article-meta>
</front>
<body><sec sec-type="intro"><title>Introduction</title>
<p>The tomato genome was sequenced as the cornerstone of an International Solanaceae Genome Initiative, a project that aims to develop the family Solanaceae as a model for systems biology for understanding plant adaptation and diversification. The tomato genome comprises approximately 950 Mb of DNA, more than 75% of which is heterochromatin and largely devoid of genes.<xref rid="b1-ebo-10-2014-177" ref-type="bibr">1</xref>
The sequencing of the tomato genome and sequencing of the wild relative were achieved and published in the SGN database (<ext-link ext-link-type="uri" xlink:href="http://solgenomics.net/tomato/">http://solgenomics.net/tomato/</ext-link>
). Of the estimated 950 Mb genome size, 760 Mb was assembled into 91 scaffolds that were aligned with the 12 tomato chromosomes.<xref rid="b2-ebo-10-2014-177" ref-type="bibr">2</xref>
</p>
<p><italic>RBR</italic>
is a plant homolog of RB, the tumor suppressor gene in animals<xref rid="b3-ebo-10-2014-177" ref-type="bibr">3</xref>
that is primarily known as a negative regulator of cell cycle progression, controlling the G1/S transition in plants and animals. RBR is part of a cell cycle network involving cyclin-dependent kinases (CDKs) that phosphorylate RBR proteins to regulate the initiation of S phase.<xref rid="b4-ebo-10-2014-177" ref-type="bibr">4</xref>
–<xref rid="b6-ebo-10-2014-177" ref-type="bibr">6</xref>
In the nonphosphorylated state, RBR1 represses the action of the transcription factor E2F, which activates the expression of many genes that are required for DNA replication, such as F-box protein 17, PCNA, and MCM5.<xref rid="b7-ebo-10-2014-177" ref-type="bibr">7</xref>
–<xref rid="b9-ebo-10-2014-177" ref-type="bibr">9</xref>
RBR functions by binding E2F transcription factors, consequently blocking the transcription of cell cycle-related genes.<xref rid="b10-ebo-10-2014-177" ref-type="bibr">10</xref>
,<xref rid="b11-ebo-10-2014-177" ref-type="bibr">11</xref>
The repression of E2F activity is because of the retinoblastoma protein-recruiting histone deacetylases (HDACs), which are co-repressors of transcription. HDACs remove acetyl groups from histones within DNA resulting in chromatin modification, DNA condensation, and transcription inhibition.<xref rid="b12-ebo-10-2014-177" ref-type="bibr">12</xref>
Furthermore, RB plays a critical role in chromosome condensation, centromeric function, and chromosome stability.<xref rid="b13-ebo-10-2014-177" ref-type="bibr">13</xref>
</p>
<p>The RB protein contains a number of functional domains, two of which, denoted as A and B, are conserved in humans and plants.<xref rid="b14-ebo-10-2014-177" ref-type="bibr">14</xref>
Similar to human RB proteins, plant RBR proteins are composed of an N-terminal region, A and B domains in the pocket region, and a C-terminal domain.<xref rid="b15-ebo-10-2014-177" ref-type="bibr">15</xref>
–<xref rid="b17-ebo-10-2014-177" ref-type="bibr">17</xref>
In the absence of RB-induced repression, E2Fs are eventually capable of inducing the expression of genes that are involved in the G1/S transition of cell cycle progression.<xref rid="b18-ebo-10-2014-177" ref-type="bibr">18</xref>
,<xref rid="b19-ebo-10-2014-177" ref-type="bibr">19</xref>
</p>
<p><italic>Arabidopsis thaliana</italic>
contains only a single <italic>RBR</italic>
gene, whereas RB has two more relatives (p107 and p130) in animals.<xref rid="b20-ebo-10-2014-177" ref-type="bibr">20</xref>
Although many plants appear to possess only one <italic>RBR</italic>
gene, maize and related cereals have at least two distinct types, <italic>RBR</italic>
1 and <italic>RBR</italic>
3.<xref rid="b21-ebo-10-2014-177" ref-type="bibr">21</xref>
–<xref rid="b23-ebo-10-2014-177" ref-type="bibr">23</xref>
</p>
<p>Plant RBR proteins control not only cell cycle arrest/progression but also development and cellular differentiation in the endosperm, leaf, and root.<xref rid="b11-ebo-10-2014-177" ref-type="bibr">11</xref>
,<xref rid="b24-ebo-10-2014-177" ref-type="bibr">24</xref>
–<xref rid="b26-ebo-10-2014-177" ref-type="bibr">26</xref>
In <italic>A. thaliana</italic>
, loss of RBR function is gametophyte lethal because mitotically derived cells from the megaspore fail to differentiate into a functional female gametophyte.<xref rid="b24-ebo-10-2014-177" ref-type="bibr">24</xref>
,<xref rid="b27-ebo-10-2014-177" ref-type="bibr">27</xref>
,<xref rid="b28-ebo-10-2014-177" ref-type="bibr">28</xref>
The loss of the RB protein also prevents or delays cell determination during plant male gametogenesis.<xref rid="b29-ebo-10-2014-177" ref-type="bibr">29</xref>
Furthermore, the loss of RBR function uncouples division and differentiation of meristemoid cells in leaves and disrupts the appropriate division and maintenance of meristem stem cells. Thus, RBR function is necessary during inflorescence and flower development to organize appropriate meristem cell divisions that are required for phyllotactic patterning and floral organ initiation. Together, these findings indicate that RBR plays a critical role in the homeostasis of stem cells and organ production in every stem cell niche.<xref rid="b30-ebo-10-2014-177" ref-type="bibr">30</xref>
</p>
<p>The <italic>rbr</italic>
-2 mutation in <italic>A. thaliana</italic>
during meiosis causes a loss of the RBR protein in male meiocytes. <italic>rbr</italic>
-2 plants exhibit strongly reduced fertility, while vegetative growth is generally unaffected. The reduced fertility is due to a meiotic defect that results in reduced chiasma formation and subsequent errors in chromosome disjunction. Immunolocalization studies in wild-type meiocytes revealed that RBR is recruited as foci to the chromosomes during early prophase I in a DNA double-stranded break-dependent manner.<xref rid="b31-ebo-10-2014-177" ref-type="bibr">31</xref>
In addition to the disruption of cell division patterns, the loss of RBR function promotes context-dependent cell proliferation and negatively influences the establishment of cell differentiation in meristematic cells, including the shoot apical meristem, meristemoid mother cells, and procambial cells, which fail to produce appropriately differentiated cells and lateral organ formation.<xref rid="b30-ebo-10-2014-177" ref-type="bibr">30</xref>
</p>
<p>Sabelli et al.<xref rid="b9-ebo-10-2014-177" ref-type="bibr">9</xref>
investigated the role of RBR1 during maize endosperm development and found that the downregulation of RBR1 by RNAi resulted in the upregulation of RBR3-type genes, as well as the MCM 2–7 gene family and PCNA, which encode essential DNA replication factors. These results indicate that the RBR1 pathway plays a major role in the regulation of different processes during maize endosperm development by controlling gene expression programs, the mitotic cell cycle, endoreduplication, cell and nuclear sizes, and programed cell death.</p>
<p>FlcDNA clones are fundamental resources for molecular biology experiments of gene functions as well as for the detection of intron–exon structures in genomes. The aim of this study was to isolate and detect the genomic structure of the tomato PcG gene <italic>Solanum lycopersicum</italic>
L. <italic>RBR</italic>
(<italic>SlRBR</italic>
) by cloning and sequencing its flcDNA of mRNA transcripts in tomato tissues. RBR is primarily known as a negative regulator of the cell cycle progression, which plays an epigenetic role in stem cell maintenance, cell specification and differentiation, and, to the best of our knowledge, this is the first gene of retinoblastoma-related gene family to be sequenced and characterized from tomato.</p>
</sec>
<sec sec-type="results"><title>Results</title>
<p>To isolate the cDNA encoding the <italic>SlRBR</italic>
gene, PCR reactions were performed using a primer set targeting the <italic>SlRBR</italic>
gene with cDNA that was synthesized from total RNA that was extracted from tomato flowers. The amplification products were cloned in the cloning vector pBluescript II SK (+) (pBS), linearized with the <italic>Eco</italic>
RV restriction enzyme, and transformed into <italic>Escherichia coli</italic>
DH5α. The <italic>SlRBR</italic>
cDNA contig was obtained by overlapping eight ESTs. The lengths of the ESTs varied between 453 bp and 1,272 bp, with an average length of 820 bp. Based on the consensus sequence of the <italic>SlRBR</italic>
cDNA contig, 5′- and 3′-RACE gene-specific primers were designed and used to amplify the ends of the <italic>SlRBR</italic>
contig. The generated 5′-and 3′-RACE fragments were 767 bp and 162 bp in length, respectively. Both the 5′- and 3′-RACE fragments were sequenced and assembled using the obtained ESTs to construct the <italic>SlRBR</italic>
flcDNA contig. Computer analysis using the BLASTn algorithm confirmed that the obtained sequence corresponded to the <italic>SlRBR</italic>
gene.</p>
<p>The constructed <italic>SlRBR</italic>
flcDNA was located on tomato chromosome 9 in a genomic region of approximately 6,739 bp. Eighteen exons were determined using a flcDNA and BLASTn search in the SGN database. The exon/intron sizes are illustrated in <xref ref-type="table" rid="t1-ebo-10-2014-177">Table 1</xref>
. The constructed <italic>SlRBR</italic>
flcDNA comprised 3,554 bp, containing 140 bp in the 5′-UTR, 3,054 bp in the ORF, and 360 bp in the 3′-UTR without a poly (A) tail. The ORF encodes a polypeptide of 1,018 amino acids, spanning from nucleotide position (np) 141, where the first ATG codon is located, to np 3,194, adjacent to a termination codon (TAA) (<xref ref-type="fig" rid="f1-ebo-10-2014-177">Fig. 1</xref>
). The flcDNA and deduced amino acid sequences were submitted to the NCBI GenBank as accession numbers JQ669018 and AFD98848, respectively.</p>
<sec sec-type="methods"><title>ORF analysis and protein homology</title>
<p>The 3,054-bp ORF from the <italic>SlRBR</italic>
flcDNA encodes 1,018 amino acids. The calculated molecular mass of the SlRBR predicted protein is 113.6 kDa with an estimated isoelectric point of 8.17. Domain prediction using NCBI CDD indicates that the SlRBR protein includes, similar to most other organisms, three conserved domains: a domain of unknown function (DUF3452) from amino acid 88 to 233, a retinoblastoma-associated protein A domain (RB A) from amino acid 426 to 616, and a CYCLIN domain from amino acid 738 to 868. These domains are conserved in homologous proteins of other plant species and appeared as conserved sequences in a multiple sequence alignment (<xref ref-type="fig" rid="f2-ebo-10-2014-177">Fig. 2</xref>
).</p>
<p>A homology analysis for the SlRBR predicted protein against the sequenced genomes of plants revealed strong homology with two solanaceous species, <italic>Nicotiana benthamiana</italic>
and <italic>N. tabacum</italic>
, which revealed the highest score values (1,748 and 1,652 bits, respectively) and shared 86% and 83% sequence identity with tomato <italic>SlRBR</italic>
, respectively. High homology revealed between dicot species and SlRBR predicted protein compared to monocot species. The dicot species shared 69–86% sequence identity with the SlRBR predicted protein, whereas the monocot species shared 61–63% identity with the SlRBR predicted protein for the best 16 hits.</p>
</sec>
<sec><title>Phylogenetic relationships between SlRBR and homologous proteins</title>
<p>Both of the phylogenetic trees (<xref ref-type="fig" rid="f3-ebo-10-2014-177">Figs. 3</xref>
and <xref ref-type="fig" rid="f4-ebo-10-2014-177">4</xref>
) confirmed the close relationship between the RBR predicted proteins of tomato and <italic>N. benthamiana</italic>
, both of which belong to the Solanaceae family. These accessions were separated from all accessions as distinct clade, with high bootstrap support in both of the constructed trees (100% in the maximum parsimony tree and 98% in the maximum likelihood tree). The monocot species <italic>Oryza sativa</italic>
appeared to be the most distant accession in both of the trees. Other accessions in the phylogenetic analysis revealed the same clustering in both of the trees, with the exception of the outgroup <italic>Volvox carteri</italic>
f. nagariensis and <italic>O. sativa</italic>
, which have been altered in their position between the trees as first and second outgroups.</p>
</sec>
<sec><title>Expression profiling for the <italic>SlRBR</italic>
gene</title>
<p>The ΔΔCT method was used to compare the expression of the <italic>SlRBR</italic>
gene in tomato tissues using leaf tissues as a calibrator. <xref ref-type="fig" rid="f5-ebo-10-2014-177">Figure 5</xref>
presents the expression levels of the <italic>SlRBR</italic>
gene, which differ significantly in various tissues. The calculated 2<sup>−ΔΔ</sup>
<italic><sup>Ct</sup>
</italic>
values showed the highest transcript abundance (38.23-fold) in closed floral bud tissues, in which cell division occurs and cell differentiation is not complete. Moderate levels (22.16-fold) were observed in flower tissues, and the lowest levels (7.46-fold) were observed in unripe fruit tissues.</p>
</sec>
</sec>
<sec sec-type="discussion"><title>Discussion</title>
<p>Since the completion of the sequencing of the <italic>A. thaliana</italic>
genome in 2000, it has become clear that information of the genome of a particular plant species can have dramatic benefits in promoting plant molecular genetics. The <italic>A. thaliana</italic>
genome sequence provides functional clues of genes from different species.<xref rid="b32-ebo-10-2014-177" ref-type="bibr">32</xref>
This study focused on the identification and characterization of a tomato gene belonging to the PcG gene family, <italic>SlRBR</italic>
, using sequence homology to the orthologous gene in <italic>A. thaliana</italic>
. Schubert et al.<xref rid="b33-ebo-10-2014-177" ref-type="bibr">33</xref>
discussed the epigenetic role of this gene in flowering and floral organ development in <italic>A. thaliana</italic>
. To the best of our knowledge, this is the first <italic>RBR</italic>
gene to be sequenced and characterized for Solanaceae with the exception of <italic>RBR</italic>
genes of the tobacco species, <italic>N. benthamiana</italic>
<xref rid="b34-ebo-10-2014-177" ref-type="bibr">34</xref>
and <italic>N. tabacum</italic>
,<xref rid="b35-ebo-10-2014-177" ref-type="bibr">35</xref>
which have been identified and published in the SGN database under the accession numbers SGN-U519343 and SGN-U432371, respectively. We obtained the complete sequence of the flcDNA of the tomato <italic>SlRBR</italic>
gene. The available ESTs sequence in the SGN database covered only 69.22% of the total length that was cloned and presented in this study. The exon/intron regions were determined, the ORF was predicted, and the 5′- and 3′-UTR of flcDNA were determined.</p>
<p><italic>RBR</italic>
is a plant homolog of RB, the tumor suppressor gene in animals<xref rid="b3-ebo-10-2014-177" ref-type="bibr">3</xref>
that is primarily known as a negative regulator of cell cycle progression, controlling the G1/S transition in plants and animals.<xref rid="b4-ebo-10-2014-177" ref-type="bibr">4</xref>
The SlRBR protein contains three conserved domains: DUF3452, RB A, and CYCLIN. These domains, as shown in the multiple sequence alignment, are present in the <italic>RBR</italic>
genes of all of the analyzed plant species. A striking degree of conservation exists in terms of the domain organization of the RB family members, including animal and plant species.<xref rid="b15-ebo-10-2014-177" ref-type="bibr">15</xref>
The conservation of RBR proteins raised the possibility that their function may also be conserved at the molecular level.</p>
<p>A homology analysis of the SlRBR predicted protein against sequenced genomes of plants revealed a high degree of homology with the tobacco species, <italic>N. benthamiana</italic>
and <italic>N. tabacum</italic>
. The low level of homology with the RBR proteins of monocot species reflected the presence of two distinct classes of <italic>RBR</italic>
genes in Graminea species. The <italic>in silico</italic>
and functional data highlight considerable differences between dicot and monocot species in the retinoblastoma regulatory pathways and permit an improved classification of the RBR proteins in higher plants. The retinoblastoma functions are shared by two distinct RBR protein subfamilies in the monocot cereal species, whereas dicot plants have only a single RBR protein. The recognition of two cereal RBR proteins indicates gene duplication, which is prevalent in plants and may lead to evolutionary innovation.<xref rid="b23-ebo-10-2014-177" ref-type="bibr">23</xref>
</p>
<p>The <italic>RBR</italic>
gene was not only identified in animals (Metazoa) but also in plants (monocots, dicots, lycophytes, mosses, and green algae), Heteroconta (oomycetes, diatoms, and brown algae), Alveolata, red algae (Rhodophyta), Heterolobosea, Haptophyta, and Amoebozoa. Only fungi appear to be an exception because only the most primitive phylum retained an <italic>RBR</italic>
, whereas the more advanced phyla evolved a functionally similar key regulator instead.<xref rid="b36-ebo-10-2014-177" ref-type="bibr">36</xref>
,<xref rid="b37-ebo-10-2014-177" ref-type="bibr">37</xref>
<italic>RBR</italic>
genes have been identified not only in the multicellular species <italic>V. carteri</italic>
<xref rid="b38-ebo-10-2014-177" ref-type="bibr">38</xref>
,<xref rid="b39-ebo-10-2014-177" ref-type="bibr">39</xref>
but also in the unicellular organism <italic>Chlamydomonas reinhardtii</italic>
.<xref rid="b40-ebo-10-2014-177" ref-type="bibr">40</xref>
This distribution of <italic>RBR</italic>
genes suggests that <italic>RBR</italic>
genes have an ancient origin. Within the bryophytes, the nonvascular embryophyte <italic>Physcomitrella patens</italic>
has at least three <italic>RBR</italic>
genes in its genome (<italic>PpRBL</italic>
1, <italic>PpRBL</italic>
2, and <italic>PpRBR</italic>
).<xref rid="b36-ebo-10-2014-177" ref-type="bibr">36</xref>
</p>
<p>To gain better insight into the dynamic expression pattern of the tomato PcG gene throughout the plant life cycle, we analyzed mRNA accumulation using QRT-PCR. Higher expression levels for the <italic>SlRBR</italic>
gene were generally observed in the flower and closed floral bud tissues, whereas lower expression levels were observed in the unripe fruit tissues. <italic>RBR</italic>
is an essential cell cycle regulatory gene that is expressed in the embryo, leaves, root and shoot meristems, and the ovule, including the embryo sac.<xref rid="b24-ebo-10-2014-177" ref-type="bibr">24</xref>
,<xref rid="b25-ebo-10-2014-177" ref-type="bibr">25</xref>
,<xref rid="b27-ebo-10-2014-177" ref-type="bibr">27</xref>
,<xref rid="b41-ebo-10-2014-177" ref-type="bibr">41</xref>
Similarly, the <italic>RBR</italic>
gene of <italic>N. benthamiana</italic>
is expressed in all plant tissues, including the roots, stems, open flowers, flower buds, and young and mature leaves.<xref rid="b34-ebo-10-2014-177" ref-type="bibr">34</xref>
We found that <italic>SlRBR</italic>
gene expression was abundant in closed floral bud tissues, pro-weak in unripe fruit tissues, and between these levels in flower tissues. Our observation of the <italic>SlRBR</italic>
gene expression patterns supports the expression of the <italic>SlRBR</italic>
gene in reproductive tissues, where <italic>RBR</italic>
mRNA was detected in developing ovules and anthers.<xref rid="b42-ebo-10-2014-177" ref-type="bibr">42</xref>
This pattern suggests that the <italic>SlRBR</italic>
gene is more active in the closed floral buds where cell divisions are expected to occur, and cell differentiation is not complete. This observation supports the conclusion that the activity of the <italic>RBR</italic>
gene is related to cell division or cell cycle progression.<xref rid="b43-ebo-10-2014-177" ref-type="bibr">43</xref>
,<xref rid="b44-ebo-10-2014-177" ref-type="bibr">44</xref>
</p>
<p>Further studies are needed to identify other PcG genes in tomato and to determine the epigenetic mechanisms and dynamic control of cell fate and differentiation in tomato at distinct developmental stages. This will hopefully aid in understanding the role of cell cycle regulators and chromatin complexes that are involved in developmental process in the Solanaceae family.</p>
</sec>
<sec sec-type="methods"><title>Experimental Procedures</title>
<sec><title>Sample collection</title>
<p>Plants of the <italic>S. lycopersicum</italic>
L., CastleRock variety from the Pacific Seed Company were grown in a greenhouse under standard culture conditions. Various tissues were collected from the plants at different stages, immediately frozen in liquid nitrogen, and stored at −80 °C until RNA extraction.</p>
</sec>
<sec sec-type="methods"><title>Primer design</title>
<p>The <italic>A. thaliana</italic>
RBR protein available in The <italic>Arabidopsis</italic>
Information Resource database (<ext-link ext-link-type="uri" xlink:href="http://www.arabidopsis.org/">http://www.arabidopsis.org/</ext-link>
) under the accession number AT3G12280 was compared with the available tomato proteins in the SGN database. A considerable similarity was found between the <italic>A. thaliana</italic>
RBR protein and BAC (C09SLf0089D12.1) and two ESTs (SGN-U570539 and SGN-U582215) in the <italic>S. lycopersicum</italic>
L. genome. The predicted <italic>SlRBR</italic>
gene in tomato was constructed based on the high similarity between the RBR protein of <italic>A. thaliana</italic>
and the mentioned BAC and ESTs using Vector NTI software version 11 (Invitrogen, Grand Island, NY, USA). The forward and reverse primers were designed for the <italic>SlRBR</italic>
gene from the predicted exon regions and used to amplify the cDNA clone from tomato flower tissues. The primers that amplify cDNAs are listed in <xref ref-type="table" rid="t2-ebo-10-2014-177">Table 2</xref>
.</p>
</sec>
<sec><title>Reverse transcription-PCR</title>
<p>Total RNA was extracted by the method of Chomczynski and Mackey<xref rid="b45-ebo-10-2014-177" ref-type="bibr">45</xref>
from various tissues with TRI reagent (Sigma, Bloomington, MN, USA), and cDNA was synthesized from the total RNA using SuperScript<sup>®</sup>
III reverse transcriptase (Invitrogen, Grand Island, NY, USA) using oligo(dT) primers. The synthesized cDNA was used as a template for the PCR to amplify the tomato <italic>SlRBR</italic>
cDNAs with the designed primers using the 2X PCR ready mix (KAPA, Wilmington, MA, USA), 0.4 μM each primer, and 3 μL of cDNA as the template with the following reaction conditions: initial denaturation at 94 °C for 5 minutes and 35 cycles of denaturation at 94 °C for 1 minute, annealing at 52 °C for 1 minute, and extension at 72 °C for 2 minutes. An extension at 72 °C for 7 minutes was performed after all of the cycles were complete. The cDNA clone was reamplified using Platinum<sup>®</sup>
<italic>Pfx</italic>
DNA polymerase (Invitrogen, Grand Island, NY, USA), which produces PCR products with blunt ends for cloning. The obtained blunt-ended fragment was purified by gel extraction using the gel extraction kit from Omega Bio-Tek (Norcross, GA, USA) according to the manufacturer’s instruction.</p>
</sec>
<sec><title>Cloning of the SlRBR cDNA</title>
<p>The cloning vector pBS from Stratagene (La Jolla, CA, USA) was prepared from bacterial cells using the QIAprep Spin Miniprep Kit (Qiagen, USA) according to the manufacturer’s instruction, and then digested using <italic>Eco</italic>
RV restriction enzyme (Promega, Madison, WI, USA) to produce blunt ends and collected from the gel. The purified cDNA fragments were ligated into the linearized plasmids with T4 DNA ligase (Promega, Madison, WI, USA). The recombinant plasmids were transformed into <italic>E. coli</italic>
DH5α host cells that were made competent using the calcium chloride method.<xref rid="b46-ebo-10-2014-177" ref-type="bibr">46</xref>
The transformation was performed using the heat-shock protocol.<xref rid="b47-ebo-10-2014-177" ref-type="bibr">47</xref>
The cells were spread onto LB plates (Display Systems Biotech, Vista, CA, USA) containing 100 μg/mL ampicillin prepared in H<sub>2</sub>
O, X-gal 20%, and IPTG 2.4% and incubated overnight at 37 °C. The recombinant plasmids were prepared from the positive clones for use as templates in the sequencing reaction.</p>
</sec>
<sec><title>5′- and 3′-RACE cDNA amplification</title>
<p>RACE was performed to determine the 5′- and 3′-noncoding region of the tomato PcG gene <italic>SlRBR</italic>
using the SMART RACE cDNA amplification kit (Clontech, Mountain View, CA, USA). The total RNA from the tomato flower tissues was used as template to synthesize first-strand cDNAs for the 5′- and 3′-ends following the manufacturer’s instructions. The <italic>SlRBR</italic>
-specific primers were designed from the sequence information of the <italic>SlRBR</italic>
contig and constructed by overlapping sequenced ESTs; the <italic>SlRBR</italic>
-specific primer 1 was used for 5′-end amplification (5′-GAAGCGGCTGAATACATGTTCGCG-3′), and the <italic>SlRBR</italic>
-specific primer 2 was used for 3′-end amplification (5′-GCTATTATGCTTGTGTGGGAGA-3′).</p>
</sec>
<sec sec-type="methods"><title>Sequence analysis and phylogenetics</title>
<p>The obtained ESTs and generated 5′- and 3′-RACE fragments were used as templates in the sequencing reaction by the dideoxynucleotide method.<xref rid="b48-ebo-10-2014-177" ref-type="bibr">48</xref>
The sequencing results were assembled using ContigExpress Vector NTI. ORF prediction and translation were performed using the Vector NTI ORF Finder tool. The deduced amino acids were subjected to BLASTp program at the <ext-link ext-link-type="uri" xlink:href="http://www.phytozome.net/database">http://www.phytozome.net/database</ext-link>
to obtain homologous protein sequences within plants. Hypothetical RBR protein sequences of plant species were aligned by ClustalW 1.83 multiple sequence alignments<xref rid="b49-ebo-10-2014-177" ref-type="bibr">49</xref>
using the BioEdit software.</p>
<p>To better understand the relationship between the SlRBR protein of tomato and the RBR proteins of other plant species, a phylogenetic analysis was performed using the protein sequences of a hypothetical gene family that were reported in the Phytozome database (code #31805130). The protein sequences for 12 members that are related to the <italic>SlRBR</italic>
gene were selected for the phylogenetic analysis. The Phytozome accession numbers for the analyzed protein sequences are as follows: <italic>A. lyrata</italic>
, 478590; <italic>A. thaliana</italic>
, AT3G12280; clementine <italic>Citrus clementina</italic>
, clementine0.9_001232m.g; orange <italic>Citrus sinensis</italic>
, orange1.1g001701m.g; soya bean <italic>Glycine max</italic>
, Glyma04g36700; rice <italic>O. sativa</italic>
, LOC_Os08g42600; poplar <italic>Populus trichocarpa</italic>
, POPTR_0001s06870; peach <italic>Prunus persica</italic>
, ppa000710m.g; castor oil <italic>Ricinus communis</italic>
, 30040.t000007; grape <italic>Vitis vinifera</italic>
, GSVIVG01035560001; and <italic>Volvox carteri</italic>
f. nagariensis, Vocar20003526 m.g. The <italic>N. benthamiana</italic>
ORF sequence is found in the SGN database under accession number SGN-U519343. A phylogenetic analysis was performed using two methods, maximum parsimony<xref rid="b50-ebo-10-2014-177" ref-type="bibr">50</xref>
,<xref rid="b51-ebo-10-2014-177" ref-type="bibr">51</xref>
and maximum likelihood,<xref rid="b52-ebo-10-2014-177" ref-type="bibr">52</xref>
with the help of the PHYLIP−3.68 package. <italic>V. carteri f. nagariensis</italic>
was used as an outgroup. The domains were predicted in the deduced SlRBR protein using NCBI CDD from the website <ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov/structure/cdd/">http://www.ncbi.nlm.nih.gov/structure/cdd/</ext-link>
.<xref rid="b53-ebo-10-2014-177" ref-type="bibr">53</xref>
–<xref rid="b55-ebo-10-2014-177" ref-type="bibr">55</xref>
</p>
</sec>
<sec><title>QRT-PCR</title>
<p>The expression level of the tomato PcG gene <italic>SlRBR</italic>
was detected using QRT-PCR. First-strand cDNA was synthesized from the total RNA that was extracted from four tomato tissues, closed floral buds, flowers, fruits, and leaves and was assayed for the <italic>SlRBR</italic>
gene expression level. The gene-specific primers (forward: 5′-TGACTGCACCTCCAGACAAG-3′ and reverse: 5′-GGCCAAGAACCTGGACAATA-3′) were used. The Actin 2/7 gene was used as a constitutively expressed gene control with the forward primer 5′-GGACTCTGGTGATGGTGTTAG-3′ and reverse primer 5′-CCGTTCAGCAGTAGTGGTG-3′. The QRT-PCR was performed in triplicate as technical replicates. Each reaction (20 μl) consisted of the 2X Hot Start SYBR ready mix (Qiagen, USA), forward and reverse primers (0.125 μM each), 3.5 μL of first-strand cDNA, and 20 μL of H<sub>2</sub>
O. The reaction conditions were as follows: 50 °C for 2 minutes and 95 °C for 15 minutes for 40 cycles (95 °C for 15 seconds and 60 °C for 30 seconds). The cycles to threshold (Ct) were used to measure the gene expression.<xref rid="b56-ebo-10-2014-177" ref-type="bibr">56</xref>
The Ct values were calculated (ΔCt) by subtracting the values of the actin 2/7 gene in each replicate. The ΔCt values were calibrated using the <italic>SlVIN</italic>
3 gene expression in the leaf tissues as a calibrator to obtain ΔΔCt, and then 2<sup>−ΔΔ</sup>
<italic><sup>Ct</sup>
</italic>
was calculated.</p>
<disp-formula id="fd1-ebo-10-2014-177"><mml:math id="mm1"><mml:mtable><mml:mtr><mml:mtd><mml:mi mathvariant="normal">Δ</mml:mi>
<mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mo>=</mml:mo>
<mml:msub><mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mrow><mml:mtext>target gene</mml:mtext>
</mml:mrow>
</mml:msub>
<mml:mo>−</mml:mo>
<mml:msub><mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mrow><mml:mtext>Actin</mml:mtext>
<mml:mn>2</mml:mn>
<mml:mo>/</mml:mo>
<mml:mn>7</mml:mn>
</mml:mrow>
</mml:msub>
</mml:mtd>
</mml:mtr>
<mml:mtr><mml:mtd><mml:mi mathvariant="normal">ΔΔ</mml:mi>
<mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mo>=</mml:mo>
<mml:mi mathvariant="normal">Δ</mml:mi>
<mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mspace width="0.2em"></mml:mspace>
<mml:mtext>tested tissue</mml:mtext>
<mml:mo>−</mml:mo>
<mml:mi mathvariant="normal">Δ</mml:mi>
<mml:mi mathvariant="normal">Ct</mml:mi>
<mml:mspace width="0.2em"></mml:mspace>
<mml:mtext>calibrator tissue</mml:mtext>
</mml:mtd>
</mml:mtr>
<mml:mtr><mml:mtd><mml:mtext>Ratio</mml:mtext>
<mml:mo>=</mml:mo>
<mml:msup><mml:mn>2</mml:mn>
<mml:mrow><mml:mo>−</mml:mo>
<mml:mi mathvariant="normal">ΔΔ</mml:mi>
<mml:mi mathvariant="normal">Ct</mml:mi>
</mml:mrow>
</mml:msup>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:math>
</disp-formula>
</sec>
</sec>
<sec><title>Conclusion</title>
<p>The molecular machinery that regulates plant flowering and development is conserved throughout the plant kingdom. The <italic>RBR</italic>
gene, a negative regulator of cell cycle progression controlling the G1/S transition in plants and animals, plays an important role in the epigenetic regulation of cell cycle genes in the differentiation and development of gametophytes and in reproduction. Here, we isolated and characterized the tomato <italic>SlRBR</italic>
gene by cloning and sequencing. The phylogenetic relationships with the homologous proteins that are available in GenBank were investigated. The expression profiling of the <italic>SlRBR</italic>
gene reflected its function in cell differentiation and development at different stages of the tomato life cycle.</p>
</sec>
<sec sec-type="supplementary-material"><title>Supplementary Data</title>
<supplementary-material content-type="local-data" id="s1-ebo-10-2014-177"><caption><p><bold>Supplementary Table 1.</bold>
The eight primer pairs that were used to amplify the cDNA clones in this study.</p>
</caption>
<media xlink:href="EBO-10-2014-177-s001.docx" mimetype="application" mime-subtype="x-zip-compressed" xlink:type="simple" id="d35e920" position="anchor"></media>
</supplementary-material>
</sec>
</body>
<back><ack><title>Acknowledgments</title>
<p>The authors are greatly indebted to Dr. Khalid Abu Khabar, director of the Biomolecular Research Department at King Faisal Specialist Hospital & Research Centre in Riyadh, and other staff members for providing the opportunity to work in the laboratory and for technical assistance with cDNA sequencing.</p>
</ack>
<fn-group><fn id="fn1-ebo-10-2014-177"><p><bold>ACADEMIC EDITOR:</bold>
Jike Cui, Associate Editor</p>
</fn>
<fn id="fn2-ebo-10-2014-177"><p><bold>FUNDING:</bold>
This work was supported by a grant from the Center of Excellence in Biotechnology Research, King Saud University (grant No. CEBR-GSRP 01/2010). The authors confirm that the funder had no influence over the study design, content of the article, or selection of this journal.</p>
</fn>
<fn id="fn3-ebo-10-2014-177"><p><bold>COMPETING INTERESTS:</bold>
Authors disclose no potential conflicts of interest.</p>
</fn>
<fn id="fn4-ebo-10-2014-177"><p>This paper was subject to independent, expert peer review by a minimum of two blind peer reviewers. All editorial decisions were made by the independent academic editor. All authors have provided signed confirmation of their compliance with ethical and legal obligations including (but not limited to) use of any copyrighted material, compliance with ICMJE authorship and competing interests disclosure guidelines and, where applicable, compliance with legal and ethical guidelines on human and animal research participants.</p>
</fn>
<fn id="fn5-ebo-10-2014-177"><p><bold>Author Contributions</bold>
</p>
<p>Conceived and designed the experiments: MTS. Analyzed the data and wrote the first draft of the manuscript: ZMA. Contributed to the writing of the manuscript, agreed with the manuscript results and conclusions, jointly developed the structure and arguments for the paper, and made critical revisions: MTS, ZMA. Both authors reviewed and approved the final manuscript.</p>
</fn>
</fn-group>
<glossary><def-list><title>Abbreviations</title>
<def-item><term>SlRBR</term>
<def><p><italic>Solanum lycopersicum</italic>
L. retinoblastoma-related</p>
</def>
</def-item>
<def-item><term>PcG</term>
<def><p>Polycomb group</p>
</def>
</def-item>
<def-item><term>RB</term>
<def><p>Retinoblastoma</p>
</def>
</def-item>
<def-item><term>SGN</term>
<def><p>Solanaceae genomics network database</p>
</def>
</def-item>
<def-item><term>PCNA</term>
<def><p>Proliferating cell nuclear antigen</p>
</def>
</def-item>
<def-item><term>MCM</term>
<def><p>Minichromosome maintenance protein</p>
</def>
</def-item>
<def-item><term>ORF</term>
<def><p>Open reading frame</p>
</def>
</def-item>
<def-item><term>FlcDNA</term>
<def><p>Full-length cDNA</p>
</def>
</def-item>
<def-item><term>EST</term>
<def><p>Expressed sequence tag</p>
</def>
</def-item>
<def-item><term>RACE</term>
<def><p>Rapid amplification of cDNA ends</p>
</def>
</def-item>
<def-item><term>CDD</term>
<def><p>Conserved domain database</p>
</def>
</def-item>
<def-item><term>QRT-PCR</term>
<def><p>Quantitative real-time PCR</p>
</def>
</def-item>
</def-list>
</glossary>
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<floats-group><fig id="f1-ebo-10-2014-177" position="float"><label>Figure 1</label>
<caption><p>Nucleotide and deduced amino acid sequences of the tomato <italic>SlRBR</italic>
gene. The flcDNA nucleotide sequence is composed of ORF (black text) and 5′- and 3′-UTR (blue text). The initiation methionine codon and the stop codon, ATG and TAA, respectively, are shown in yellow. The numbers on the left refer to the nucleotide positions. The amino acid sequence of the tomato SlRBR predicted protein is shown above the ORF sequence (red text). The conserved domains DUF3452, RB A and CYCLIN are shown in green, pink and turquoise, respectively.</p>
</caption>
<graphic xlink:href="ebo-10-2014-177f1"></graphic>
</fig>
<fig id="f2-ebo-10-2014-177" position="float"><label>Figure 2</label>
<caption><p>Multiple sequence alignments of the conserved domains sequences of the SlRBR predicted protein and 12 protein sequences of RBR hypothetical gene family members. The alignment was performed using ClustalW 1.83 in the BioEdit software. The conserved domains were identified in the sequence of the SlRBR protein using NCBI CDD. (<bold>A</bold>
) Conserved domains of the SlRBR protein; (<bold>B</bold>
) RB A domain from amino acid 426 to 616; (<bold>C</bold>
) CYCLIN domain from amino acid 738 to 868.</p>
</caption>
<graphic xlink:href="ebo-10-2014-177f2"></graphic>
</fig>
<fig id="f3-ebo-10-2014-177" position="float"><label>Figure 3</label>
<caption><p>Unrooted phylogenetic tree of the 12 hypothetical RBR protein sequences with the tomato SlRBR predicted protein sequence that was constructed using the maximum parsimony method. <italic>V. carteri f. nagariensis</italic>
was used as an outgroup. The numbers on the nodes are bootstrap percentages supporting a given partitioning.</p>
</caption>
<graphic xlink:href="ebo-10-2014-177f3"></graphic>
</fig>
<fig id="f4-ebo-10-2014-177" position="float"><label>Figure 4</label>
<caption><p>Unrooted phylogenetic tree of 12 hypothetical RBR protein sequences with the tomato SlRBR predicted protein sequence that was obtained using the maximum likelihood method. <italic>V. carteri f. nagariensis</italic>
was used as an outgroup. The numbers on the branches are bootstrap percentages supporting a given partitioning. The scale below the tree measures the distance between the protein sequences where the lengths of branches proportionate to the number of amino acid changes that have occurred along the branch.</p>
</caption>
<graphic xlink:href="ebo-10-2014-177f4"></graphic>
</fig>
<fig id="f5-ebo-10-2014-177" position="float"><label>Figure 5</label>
<caption><p>Expression analysis of the tomato PcG gene <italic>SlRBR</italic>
in various tomato tissues. The relative transcript levels (<italic>y</italic>
axis), which are an average of three replicates, showed high expression levels of the <italic>SlRBR</italic>
gene in the closed floral bud tissue (38.23-fold) and a moderate expression level in the flower tissue (22.16-fold), whereas the lowest expression level (7.46-fold) was in the unripe fruits.</p>
</caption>
<graphic xlink:href="ebo-10-2014-177f5"></graphic>
</fig>
<table-wrap id="t1-ebo-10-2014-177" position="float"><label>Table 1</label>
<caption><p>Sizes of the exon/intron for the <italic>SlRBR</italic>
gene. Eighteen exons were determined by presence within flcDNA using BLASTn search in the SGN database. Complete nucleotide sequence was derived from eight ESTs with 5′-and 3′-RACE fragments.</p>
</caption>
<table frame="box" rules="rows"><thead><tr><th align="left" valign="top" rowspan="1" colspan="1">EXON NO.</th>
<th align="left" valign="top" rowspan="1" colspan="1">COORDINATE</th>
<th align="left" valign="top" rowspan="1" colspan="1">SIZE BP</th>
<th align="left" valign="top" rowspan="1" colspan="1">INTRON NO.</th>
<th align="left" valign="top" rowspan="1" colspan="1">SIZE BP</th>
</tr>
</thead>
<tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">5’UTR</td>
<td align="left" valign="top" rowspan="1" colspan="1">−140 ..−1</td>
<td align="left" valign="top" rowspan="1" colspan="1">140</td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon01</td>
<td align="left" valign="top" rowspan="1" colspan="1">1 .. 89</td>
<td align="left" valign="top" rowspan="1" colspan="1">89</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron01</td>
<td align="left" valign="top" rowspan="1" colspan="1">659</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon02</td>
<td align="left" valign="top" rowspan="1" colspan="1">90 .. 197</td>
<td align="left" valign="top" rowspan="1" colspan="1">108</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron02</td>
<td align="left" valign="top" rowspan="1" colspan="1">100</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon03</td>
<td align="left" valign="top" rowspan="1" colspan="1">198 .. 338</td>
<td align="left" valign="top" rowspan="1" colspan="1">141</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron03</td>
<td align="left" valign="top" rowspan="1" colspan="1">82</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon04</td>
<td align="left" valign="top" rowspan="1" colspan="1">339 .. 435</td>
<td align="left" valign="top" rowspan="1" colspan="1">97</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron04</td>
<td align="left" valign="top" rowspan="1" colspan="1">240</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon05</td>
<td align="left" valign="top" rowspan="1" colspan="1">436 .. 483</td>
<td align="left" valign="top" rowspan="1" colspan="1">48</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron05</td>
<td align="left" valign="top" rowspan="1" colspan="1">119</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon06</td>
<td align="left" valign="top" rowspan="1" colspan="1">484 .. 680</td>
<td align="left" valign="top" rowspan="1" colspan="1">197</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron06</td>
<td align="left" valign="top" rowspan="1" colspan="1">503</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon07</td>
<td align="left" valign="top" rowspan="1" colspan="1">681 .. 748</td>
<td align="left" valign="top" rowspan="1" colspan="1">68</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron07</td>
<td align="left" valign="top" rowspan="1" colspan="1">123</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon08</td>
<td align="left" valign="top" rowspan="1" colspan="1">749 .. 923</td>
<td align="left" valign="top" rowspan="1" colspan="1">175</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron08</td>
<td align="left" valign="top" rowspan="1" colspan="1">73</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon09</td>
<td align="left" valign="top" rowspan="1" colspan="1">924 .. 1,118</td>
<td align="left" valign="top" rowspan="1" colspan="1">195</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron09</td>
<td align="left" valign="top" rowspan="1" colspan="1">93</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon10</td>
<td align="left" valign="top" rowspan="1" colspan="1">1,119 .. 2,004</td>
<td align="left" valign="top" rowspan="1" colspan="1">886</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron10</td>
<td align="left" valign="top" rowspan="1" colspan="1">129</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon11</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,005 .. 2,164</td>
<td align="left" valign="top" rowspan="1" colspan="1">160</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron11</td>
<td align="left" valign="top" rowspan="1" colspan="1">99</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon12</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,165 .. 2,237</td>
<td align="left" valign="top" rowspan="1" colspan="1">73</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron12</td>
<td align="left" valign="top" rowspan="1" colspan="1">443</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon13</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,238 .. 2,414</td>
<td align="left" valign="top" rowspan="1" colspan="1">177</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron13</td>
<td align="left" valign="top" rowspan="1" colspan="1">86</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon14</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,415 .. 2,535</td>
<td align="left" valign="top" rowspan="1" colspan="1">121</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron14</td>
<td align="left" valign="top" rowspan="1" colspan="1">85</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon15</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,536 .. 2,674</td>
<td align="left" valign="top" rowspan="1" colspan="1">139</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron15</td>
<td align="left" valign="top" rowspan="1" colspan="1">128</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon16</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,675 .. 2,786</td>
<td align="left" valign="top" rowspan="1" colspan="1">112</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron16</td>
<td align="left" valign="top" rowspan="1" colspan="1">151</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon17</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,787 .. 2,903</td>
<td align="left" valign="top" rowspan="1" colspan="1">117</td>
<td align="left" valign="top" rowspan="1" colspan="1">Intron17</td>
<td align="left" valign="top" rowspan="1" colspan="1">74</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">Exon18</td>
<td align="left" valign="top" rowspan="1" colspan="1">2,904 .. 3,054</td>
<td align="left" valign="top" rowspan="1" colspan="1">151</td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1">3’UTR</td>
<td align="left" valign="top" rowspan="1" colspan="1">3,055 .. 3,414</td>
<td align="left" valign="top" rowspan="1" colspan="1">360</td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
<td align="left" valign="top" rowspan="1" colspan="1"></td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="t2-ebo-10-2014-177" position="float"><label>Table 2</label>
<caption><p>The eight primer pairs used to amplify cDNA clones in this study. “F” and “R” in the primer names indicate direction (forward or reverse) of the primer.</p>
</caption>
<table frame="box" rules="rows"><thead><tr><th align="left" valign="top" rowspan="1" colspan="1">PRIMER NAME</th>
<th align="left" valign="top" rowspan="1" colspan="1">PRIMER SEQUENCE</th>
</tr>
</thead>
<tbody><tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F01</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- GCT TAT CAG AGC CCC TCA AA -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R01</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′ -GAA GAG AAC GAG CAT CGT TG -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F02</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- GGT TCA GAA CAT GTG GAT ATC A -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R02</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- AAG CAT CGG GTT GGT GGC GG -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F03</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- GGC ATG ATT GAG CGG CTA CA -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R03</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- TAC CGC TCA TTC AAC ACC CC -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F04</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- ATG CAC ATT AAC CCA TCT TTG GGA -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R04</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- AAG AGC AAA GGA TGA TCT GG -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F05</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- GGG CAA AGA ACC TGG ACA ATA TCG ACG C -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R05</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- TCC CAA AGA TGG GTT AAT GTG CAT -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F06</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- GAA CAA GGG TGA ATT GGA TGA GAG G -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R06</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- TGT AGC CGC TCA ATC ATG CC -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F07</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- AGA ATG AAG CTA GGA ATT CG -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R07</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- CCT CTC ATC CAA TTC ACC CTT GTT C -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
F08</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- TGA AGA GAA TGG TTC GGT GG -3′</td>
</tr>
<tr><td align="left" valign="top" rowspan="1" colspan="1"><italic>SlRBR</italic>
R08</td>
<td align="left" valign="top" rowspan="1" colspan="1">5′- ACG ATA AAG ATG ATT CCT CC -3′</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</pmc>
</record>
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