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Combined analysis of Polygonum cuspidatum transcriptome and metabolome revealed that PcMYB62, a transcription factor, responds to methyl jasmonate and inhibits resveratrol biosynthesis

A comparative transcriptomic and metabolomic analysis of Polygonum cuspidatum leaves treated with MeJA was carried out to investigate the regulatory mechanisms of its active compounds. A total of 692 metabolites and 77,198 unigenes were obtained, including 200 differentially accumulated metabolites...

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Published in:International journal of biological macromolecules 2024-06, Vol.270 (Pt 2), p.132450, Article 132450
Main Authors: Lin, Fan, Chen, Jianhui, Wang, Xiaowei, Ma, Hongping, Liang, Shuang, Hu, Hongyan, Fan, Haili, Wu, Zhijun, Chai, Tuanyao, Wang, Hong
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container_issue Pt 2
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container_title International journal of biological macromolecules
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creator Lin, Fan
Chen, Jianhui
Wang, Xiaowei
Ma, Hongping
Liang, Shuang
Hu, Hongyan
Fan, Haili
Wu, Zhijun
Chai, Tuanyao
Wang, Hong
description A comparative transcriptomic and metabolomic analysis of Polygonum cuspidatum leaves treated with MeJA was carried out to investigate the regulatory mechanisms of its active compounds. A total of 692 metabolites and 77,198 unigenes were obtained, including 200 differentially accumulated metabolites and 6819 differentially expressed genes. We screened potential regulatory transcription factors involved in resveratrol and flavonoids biosynthesis, and successfully identified an MYB transcription factor, PcMYB62, which could significantly decrease the resveratrol content in P. cuspidatum leaves when over-expressed. PcMYB62 could directly bind to the MBS motifs in the promoter region of stilbene synthase (PcSTS) gene and repress its expression. Besides, PcMYB62 could also repress PcSTS expression and resveratrol biosynthesis in transgenic Arabidopsis thaliana. Our results provide abundant candidate genes for further investigation, and the new finding of the inhibitory role of PcMYB62 on the resveratrol biosynthesis could also potentially be used in metabolic engineering of resveratrol in P. cuspidatum.
doi_str_mv 10.1016/j.ijbiomac.2024.132450
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Our results provide abundant candidate genes for further investigation, and the new finding of the inhibitory role of PcMYB62 on the resveratrol biosynthesis could also potentially be used in metabolic engineering of resveratrol in P. cuspidatum.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38772462</pmid><doi>10.1016/j.ijbiomac.2024.132450</doi></addata></record>
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ispartof International journal of biological macromolecules, 2024-06, Vol.270 (Pt 2), p.132450, Article 132450
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subjects Acetates - metabolism
Acetates - pharmacology
Acyltransferases - genetics
Acyltransferases - metabolism
Arabidopsis - drug effects
Arabidopsis - genetics
Arabidopsis - metabolism
Arabidopsis thaliana
biosynthesis
Cyclopentanes - metabolism
Cyclopentanes - pharmacology
Fallopia japonica - genetics
Fallopia japonica - metabolism
flavonoids
Gene Expression Profiling
gene expression regulation
Gene Expression Regulation, Plant - drug effects
genetically modified organisms
MeJA
metabolites
Metabolome
Metabolome - drug effects
metabolomics
methyl jasmonate
Oxylipins - metabolism
Oxylipins - pharmacology
PcMYB62
Plant Leaves - drug effects
Plant Leaves - genetics
Plant Leaves - metabolism
Plant Proteins - genetics
Plant Proteins - metabolism
Plants, Genetically Modified - genetics
Polygonum cuspidatum
promoter regions
Resveratrol
Resveratrol - metabolism
Resveratrol - pharmacology
Reynoutria japonica
transcription factors
Transcription Factors - genetics
Transcription Factors - metabolism
Transcriptome
Transcriptome - drug effects
transcriptomics
trihydroxystilbene synthase
unigenes
title Combined analysis of Polygonum cuspidatum transcriptome and metabolome revealed that PcMYB62, a transcription factor, responds to methyl jasmonate and inhibits resveratrol biosynthesis
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