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Coexpression analysis of a large-scale transcriptome identified a calmodulin-like protein regulating the development of adventitious roots in poplar.

Identifieur interne : 000513 ( Main/Exploration ); précédent : 000512; suivant : 000514

Coexpression analysis of a large-scale transcriptome identified a calmodulin-like protein regulating the development of adventitious roots in poplar.

Auteurs : Zheng'Ang Xiao [République populaire de Chine] ; Yan Zhang [République populaire de Chine] ; Meifeng Liu [République populaire de Chine] ; Chang Zhan [République populaire de Chine] ; Xiaoqing Yang [République populaire de Chine] ; Tashbek Nvsvrot [République populaire de Chine] ; Zhaogui Yan [République populaire de Chine] ; Nian Wang [République populaire de Chine]

Source :

RBID : pubmed:32578840

Abstract

Poplars are important woody plants, and the ability to form adventitious roots (ARs) is the key factor for their cultivation because most poplars are propagated by cloning. In previous studies, Ca2+ was confirmed to regulate AR formation in poplar. In this study, wild-type poplar cuttings grown in 1.0 mM Ca2+ solution showed the best visible performance of AR development. Coexpression analysis of a large-scale RNA-Seq transcriptome was conducted to identify Ca2+-related genes that regulate AR development in poplar. A total of 15 coexpression modules (CMs) were identified, and two CMs showed high association with AR development. Functional analysis identified a number of biological pathways, including 'oxidation-reduction process', 'response to biotic stimulus' and 'metabolic process', in tissues of AR development. The Ca2+-related pathway was specifically selected, and its regulation in poplar AR development was predicted. A Ca2+ sensor, PdeCML23-1, which is a member of the calmodulin-like protein (CML) family, was found to promote AR development by phenotypic assay of overexpressed PdeCML23-1 transgenic lines at various growing conditions. By measuring cytosolic Ca2+ in AR tips, PdeCML23-1 seemed to play a role in decreasing cytosolic Ca2+ concentration. Additionally, the expression profiles of some genes and phytohormone indole acetic acid (IAA) were also changed in the overexpressed PdeCML23-1 transgenic lines. According to this study, we were able to provide a global view of gene regulation for poplar AR development. Moreover, we also observed the regulation of cytosolic Ca2+ concentration by PdeCML23-1, and this regulation was involved in AR development in poplar. We also predicted that PdeCML23-1 possibly regulates AR development by modulating IAA content in poplar.

DOI: 10.1093/treephys/tpaa078
PubMed: 32578840


Affiliations:


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<div type="abstract" xml:lang="en">Poplars are important woody plants, and the ability to form adventitious roots (ARs) is the key factor for their cultivation because most poplars are propagated by cloning. In previous studies, Ca2+ was confirmed to regulate AR formation in poplar. In this study, wild-type poplar cuttings grown in 1.0 mM Ca2+ solution showed the best visible performance of AR development. Coexpression analysis of a large-scale RNA-Seq transcriptome was conducted to identify Ca2+-related genes that regulate AR development in poplar. A total of 15 coexpression modules (CMs) were identified, and two CMs showed high association with AR development. Functional analysis identified a number of biological pathways, including 'oxidation-reduction process', 'response to biotic stimulus' and 'metabolic process', in tissues of AR development. The Ca2+-related pathway was specifically selected, and its regulation in poplar AR development was predicted. A Ca2+ sensor, PdeCML23-1, which is a member of the calmodulin-like protein (CML) family, was found to promote AR development by phenotypic assay of overexpressed PdeCML23-1 transgenic lines at various growing conditions. By measuring cytosolic Ca2+ in AR tips, PdeCML23-1 seemed to play a role in decreasing cytosolic Ca2+ concentration. Additionally, the expression profiles of some genes and phytohormone indole acetic acid (IAA) were also changed in the overexpressed PdeCML23-1 transgenic lines. According to this study, we were able to provide a global view of gene regulation for poplar AR development. Moreover, we also observed the regulation of cytosolic Ca2+ concentration by PdeCML23-1, and this regulation was involved in AR development in poplar. We also predicted that PdeCML23-1 possibly regulates AR development by modulating IAA content in poplar.</div>
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</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
<region>
<li>Hubei</li>
</region>
<settlement>
<li>Wuhan</li>
</settlement>
</list>
<tree>
<country name="République populaire de Chine">
<region name="Hubei">
<name sortKey="Xiao, Zheng Ang" sort="Xiao, Zheng Ang" uniqKey="Xiao Z" first="Zheng'Ang" last="Xiao">Zheng'Ang Xiao</name>
</region>
<name sortKey="Liu, Meifeng" sort="Liu, Meifeng" uniqKey="Liu M" first="Meifeng" last="Liu">Meifeng Liu</name>
<name sortKey="Nvsvrot, Tashbek" sort="Nvsvrot, Tashbek" uniqKey="Nvsvrot T" first="Tashbek" last="Nvsvrot">Tashbek Nvsvrot</name>
<name sortKey="Wang, Nian" sort="Wang, Nian" uniqKey="Wang N" first="Nian" last="Wang">Nian Wang</name>
<name sortKey="Wang, Nian" sort="Wang, Nian" uniqKey="Wang N" first="Nian" last="Wang">Nian Wang</name>
<name sortKey="Yan, Zhaogui" sort="Yan, Zhaogui" uniqKey="Yan Z" first="Zhaogui" last="Yan">Zhaogui Yan</name>
<name sortKey="Yang, Xiaoqing" sort="Yang, Xiaoqing" uniqKey="Yang X" first="Xiaoqing" last="Yang">Xiaoqing Yang</name>
<name sortKey="Zhan, Chang" sort="Zhan, Chang" uniqKey="Zhan C" first="Chang" last="Zhan">Chang Zhan</name>
<name sortKey="Zhang, Yan" sort="Zhang, Yan" uniqKey="Zhang Y" first="Yan" last="Zhang">Yan Zhang</name>
</country>
</tree>
</affiliations>
</record>

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