Transcription factor CsNAC25 mediating dual roles in tea plant secondary cell wall formation and trichome development

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kangli Peng , Guoxiang Xiao , Yin Shi , Xiaozhen Huang
{"title":"Transcription factor CsNAC25 mediating dual roles in tea plant secondary cell wall formation and trichome development","authors":"Kangli Peng ,&nbsp;Guoxiang Xiao ,&nbsp;Yin Shi ,&nbsp;Xiaozhen Huang","doi":"10.1016/j.plantsci.2025.112499","DOIUrl":null,"url":null,"abstract":"<div><div>Trichomes are a key feature of tea plants (<em>Camellia sinensis</em> L.) and essential for tea flavor compound formation, but their developmental mechanisms are still unclear. This study identified a transcription factor, <em>CsNAC25</em>, which positively regulates trichome formation in the ‘Qiancha 1’ tea plant cultivar. Phylogenetic analysis showed that <em>CsNAC25</em> shares the highest homology with <em>Arabidopsis XND1</em>, and in situ hybridization revealed its specific expression in xylem cells and in trichomes of tea plant. Overexpression of <em>CsNAC25</em> significantly inhibited xylem cell differentiation, reduced lignin and cellulose content, and led to a marked increase in trichome density. Conversely, using virus-induced gene silencing to silence <em>CsNAC25</em> in tea plants resulted in reduced trichome density and elevated lignin content. Quantitative real-time PCR analysis showed that the expression of key phenylpropanoid pathway genes, such as <em>NtPAL2</em>, <em>Nt4CL1</em>, <em>NtCAD1</em>, and <em>NtCCR1</em>, was significantly reduced in the overexpression lines. Conversely, in the <em>CsNAC25</em>-silenced tea cuttings, the expression of <em>CsPAL1</em>, <em>Cs4CL2</em>, <em>CsCAD1</em>, and <em>CsCCR1</em> was drastically increased. Moreover, the expression of <em>CsMYB1</em>, a positive regulator of trichome development, was significantly decreased in the <em>CsNAC25</em>-silenced lines. Further yeast one-hybrid and dual luciferase assays showed that <em>CsNAC25</em> binds to the <em>CsCCR1</em> promoter and represses its expression, suggesting that <em>CsNAC25</em> regulates trichome development possibly by modulating <em>CsCCR1</em> and impacting resource allocation within the phenylpropanoid metabolic network. In summary, our findings indicate that <em>CsNAC25</em> in tea plants plays a dual role in regulating the secondary cell wall formation and trichome development.</div></div>","PeriodicalId":20273,"journal":{"name":"Plant Science","volume":"356 ","pages":"Article 112499"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Science","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168945225001177","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Trichomes are a key feature of tea plants (Camellia sinensis L.) and essential for tea flavor compound formation, but their developmental mechanisms are still unclear. This study identified a transcription factor, CsNAC25, which positively regulates trichome formation in the ‘Qiancha 1’ tea plant cultivar. Phylogenetic analysis showed that CsNAC25 shares the highest homology with Arabidopsis XND1, and in situ hybridization revealed its specific expression in xylem cells and in trichomes of tea plant. Overexpression of CsNAC25 significantly inhibited xylem cell differentiation, reduced lignin and cellulose content, and led to a marked increase in trichome density. Conversely, using virus-induced gene silencing to silence CsNAC25 in tea plants resulted in reduced trichome density and elevated lignin content. Quantitative real-time PCR analysis showed that the expression of key phenylpropanoid pathway genes, such as NtPAL2, Nt4CL1, NtCAD1, and NtCCR1, was significantly reduced in the overexpression lines. Conversely, in the CsNAC25-silenced tea cuttings, the expression of CsPAL1, Cs4CL2, CsCAD1, and CsCCR1 was drastically increased. Moreover, the expression of CsMYB1, a positive regulator of trichome development, was significantly decreased in the CsNAC25-silenced lines. Further yeast one-hybrid and dual luciferase assays showed that CsNAC25 binds to the CsCCR1 promoter and represses its expression, suggesting that CsNAC25 regulates trichome development possibly by modulating CsCCR1 and impacting resource allocation within the phenylpropanoid metabolic network. In summary, our findings indicate that CsNAC25 in tea plants plays a dual role in regulating the secondary cell wall formation and trichome development.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信