CsNAC29 transcription factor activates α‐farnesene emission to resist gray blight disease in tea plant ( Camellia sinensis )

Fuente: Wiley Open Access
Saved in:
Bibliographic Details
Main Authors: Qingshan Xu, Zinan Zhuang, Long Cheng, Jiayi Jin, Huicong Ma, Huirui Chen, Wen Xiang, Xinyu Wang, Ziyan Zhao, Junyan Zhu, Shuyuan Liu, Youben Yu
Format: Artículo Open Access
Published: Wiley 2025
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867005032646311936
author Qingshan Xu
Zinan Zhuang
Long Cheng
Jiayi Jin
Huicong Ma
Huirui Chen
Wen Xiang
Xinyu Wang
Ziyan Zhao
Junyan Zhu
Shuyuan Liu
Youben Yu
author_facet Qingshan Xu
Zinan Zhuang
Long Cheng
Jiayi Jin
Huicong Ma
Huirui Chen
Wen Xiang
Xinyu Wang
Ziyan Zhao
Junyan Zhu
Shuyuan Liu
Youben Yu
Qingshan Xu
Zinan Zhuang
Long Cheng
Jiayi Jin
Huicong Ma
Huirui Chen
Wen Xiang
Xinyu Wang
Ziyan Zhao
Junyan Zhu
Shuyuan Liu
Youben Yu
collection Wiley Open Access
contents CsNAC29 transcription factor activates α‐farnesene emission to resist gray blight disease in tea plant ( Camellia sinensis ) Qingshan Xu Zinan Zhuang Long Cheng Jiayi Jin Huicong Ma Huirui Chen Wen Xiang Xinyu Wang Ziyan Zhao Junyan Zhu Shuyuan Liu Youben Yu The Plant Journal SUMMARY α‐Farnesene is one of the most widely distributed volatile organic compounds (VOCs) in plants, playing a significant role in both flavor formation and defense mechanisms. However, the regulatory mechanisms and physiological functions of α‐farnesene biosynthesis in tea plants remain largely unexplored. In this study, α‐farnesene was identified as a key compound associated with resistance to gray blight disease. We characterized an α‐farnesene synthase gene ( CsAFS2.1 ) and its alternative splicing isoforms ( CsAFS2.2 and CsAFS2.3 ), which were differentially induced upon pathogen infection, with CsAFS2.1 showing the highest level of induction. Through subcellular localization studies, in vitro enzymatic assays, and in vivo functional verification, we demonstrated that all three isoforms catalyze the conversion of farnesyl pyrophosphate (FPP) to α‐farnesene in tea plants. Using an integrative approach that included DNA–protein interaction analysis, gene silencing, gene overexpression, and metabolic profiling, we revealed that the transcription factor CsNAC29 activates α‐farnesene emission by directly regulating the expression of CsAFS2 . Suppression of either CsNAC29 or CsAFS2 significantly reduced α‐farnesene production and compromised the resistance of tea plants to gray blight disease. Our study not only elucidates the molecular mechanisms underlying α‐farnesene‐mediated resistance in tea plants but also proposes a potential pathway for enhancing both aroma and immunity through targeted genetic manipulation. 10.1111/tpj.70421 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1111/tpj.70421
format Artículo Open Access
id wiley_oa_10_1111_tpj_70421
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2025
publisher Wiley
record_format wiley_oa
spellingShingle CsNAC29 transcription factor activates α‐farnesene emission to resist gray blight disease in tea plant ( Camellia sinensis )
Qingshan Xu
Zinan Zhuang
Long Cheng
Jiayi Jin
Huicong Ma
Huirui Chen
Wen Xiang
Xinyu Wang
Ziyan Zhao
Junyan Zhu
Shuyuan Liu
Youben Yu
The Plant Journal
CsNAC29 transcription factor activates α‐farnesene emission to resist gray blight disease in tea plant ( Camellia sinensis ) Qingshan Xu Zinan Zhuang Long Cheng Jiayi Jin Huicong Ma Huirui Chen Wen Xiang Xinyu Wang Ziyan Zhao Junyan Zhu Shuyuan Liu Youben Yu The Plant Journal SUMMARY α‐Farnesene is one of the most widely distributed volatile organic compounds (VOCs) in plants, playing a significant role in both flavor formation and defense mechanisms. However, the regulatory mechanisms and physiological functions of α‐farnesene biosynthesis in tea plants remain largely unexplored. In this study, α‐farnesene was identified as a key compound associated with resistance to gray blight disease. We characterized an α‐farnesene synthase gene ( CsAFS2.1 ) and its alternative splicing isoforms ( CsAFS2.2 and CsAFS2.3 ), which were differentially induced upon pathogen infection, with CsAFS2.1 showing the highest level of induction. Through subcellular localization studies, in vitro enzymatic assays, and in vivo functional verification, we demonstrated that all three isoforms catalyze the conversion of farnesyl pyrophosphate (FPP) to α‐farnesene in tea plants. Using an integrative approach that included DNA–protein interaction analysis, gene silencing, gene overexpression, and metabolic profiling, we revealed that the transcription factor CsNAC29 activates α‐farnesene emission by directly regulating the expression of CsAFS2 . Suppression of either CsNAC29 or CsAFS2 significantly reduced α‐farnesene production and compromised the resistance of tea plants to gray blight disease. Our study not only elucidates the molecular mechanisms underlying α‐farnesene‐mediated resistance in tea plants but also proposes a potential pathway for enhancing both aroma and immunity through targeted genetic manipulation. 10.1111/tpj.70421 http://onlinelibrary.wiley.com/termsAndConditions#vor
title CsNAC29 transcription factor activates α‐farnesene emission to resist gray blight disease in tea plant ( Camellia sinensis )
topic The Plant Journal
url https://onlinelibrary.wiley.com/doi/10.1111/tpj.70421