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Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood

Tension wood (TW) is a specialized xylem tissue developed under mechanical/tension stress in angiosperm trees. TW development involves transregulation of secondary cell wall genes, which leads to altered wood properties for stress adaptation. We induced TW in the stems of black cottonwood (Populus t...

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Autores principales: Liu, Baoguang, Liu, Juan, Yu, Jing, Wang, Zhifeng, Sun, Yi, Li, Shuang, Lin, Ying-Chung Jimmy, Chiang, Vincent L, Li, Wei, Wang, Jack P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154086/
https://www.ncbi.nlm.nih.gov/pubmed/33793955
http://dx.doi.org/10.1093/plphys/kiab038
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author Liu, Baoguang
Liu, Juan
Yu, Jing
Wang, Zhifeng
Sun, Yi
Li, Shuang
Lin, Ying-Chung Jimmy
Chiang, Vincent L
Li, Wei
Wang, Jack P
author_facet Liu, Baoguang
Liu, Juan
Yu, Jing
Wang, Zhifeng
Sun, Yi
Li, Shuang
Lin, Ying-Chung Jimmy
Chiang, Vincent L
Li, Wei
Wang, Jack P
author_sort Liu, Baoguang
collection PubMed
description Tension wood (TW) is a specialized xylem tissue developed under mechanical/tension stress in angiosperm trees. TW development involves transregulation of secondary cell wall genes, which leads to altered wood properties for stress adaptation. We induced TW in the stems of black cottonwood (Populus trichocarpa, Nisqually-1) and identified two significantly repressed transcription factor (TF) genes: class B3 heat-shock TF (HSFB3-1) and MYB092. Transcriptomic analysis and chromatin immunoprecipitation (ChIP) were used to identify direct TF–DNA interactions in P. trichocarpa xylem protoplasts overexpressing the TFs. This analysis established a transcriptional regulatory network in which PtrHSFB3-1 and PtrMYB092 directly activate 8 and 11 monolignol genes, respectively. The TF–DNA interactions were verified for their specificity and transactivator roles in 35 independent CRISPR-based biallelic mutants and overexpression transgenic lines of PtrHSFB3-1 and PtrMYB092 in P. trichocarpa. The gene-edited trees (mimicking the repressed PtrHSFB3-1 and PtrMYB092 under tension stress) have stem wood composition resembling that of TW during normal growth and under tension stress (i.e., low lignin and high cellulose), whereas the overexpressors showed an opposite effect (high lignin and low cellulose). Individual overexpression of the TFs impeded lignin reduction under tension stress and restored high levels of lignin biosynthesis in the TW. This study offers biological insights to further uncover how metabolism, growth, and stress adaptation are coordinately regulated in trees.
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spelling pubmed-81540862021-05-28 Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood Liu, Baoguang Liu, Juan Yu, Jing Wang, Zhifeng Sun, Yi Li, Shuang Lin, Ying-Chung Jimmy Chiang, Vincent L Li, Wei Wang, Jack P Plant Physiol Regular Issue Tension wood (TW) is a specialized xylem tissue developed under mechanical/tension stress in angiosperm trees. TW development involves transregulation of secondary cell wall genes, which leads to altered wood properties for stress adaptation. We induced TW in the stems of black cottonwood (Populus trichocarpa, Nisqually-1) and identified two significantly repressed transcription factor (TF) genes: class B3 heat-shock TF (HSFB3-1) and MYB092. Transcriptomic analysis and chromatin immunoprecipitation (ChIP) were used to identify direct TF–DNA interactions in P. trichocarpa xylem protoplasts overexpressing the TFs. This analysis established a transcriptional regulatory network in which PtrHSFB3-1 and PtrMYB092 directly activate 8 and 11 monolignol genes, respectively. The TF–DNA interactions were verified for their specificity and transactivator roles in 35 independent CRISPR-based biallelic mutants and overexpression transgenic lines of PtrHSFB3-1 and PtrMYB092 in P. trichocarpa. The gene-edited trees (mimicking the repressed PtrHSFB3-1 and PtrMYB092 under tension stress) have stem wood composition resembling that of TW during normal growth and under tension stress (i.e., low lignin and high cellulose), whereas the overexpressors showed an opposite effect (high lignin and low cellulose). Individual overexpression of the TFs impeded lignin reduction under tension stress and restored high levels of lignin biosynthesis in the TW. This study offers biological insights to further uncover how metabolism, growth, and stress adaptation are coordinately regulated in trees. Oxford University Press 2021-02-02 /pmc/articles/PMC8154086/ /pubmed/33793955 http://dx.doi.org/10.1093/plphys/kiab038 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue
Liu, Baoguang
Liu, Juan
Yu, Jing
Wang, Zhifeng
Sun, Yi
Li, Shuang
Lin, Ying-Chung Jimmy
Chiang, Vincent L
Li, Wei
Wang, Jack P
Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title_full Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title_fullStr Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title_full_unstemmed Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title_short Transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
title_sort transcriptional reprogramming of xylem cell wall biosynthesis in tension wood
topic Regular Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154086/
https://www.ncbi.nlm.nih.gov/pubmed/33793955
http://dx.doi.org/10.1093/plphys/kiab038
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