The UDP-glycosyltransferase PpUGT74F2 is involved in fruit immunity via modulating salicylic acid metabolism

IF 8.7 1区 农林科学 Q1 Agricultural and Biological Sciences
Dan Jiang, Siyin Lin, Linfeng Xie, Miaojing Chen, Yanna Shi, Kunsong Chen, Xian Li, Boping Wu, Bo Zhang
{"title":"The UDP-glycosyltransferase PpUGT74F2 is involved in fruit immunity via modulating salicylic acid metabolism","authors":"Dan Jiang, Siyin Lin, Linfeng Xie, Miaojing Chen, Yanna Shi, Kunsong Chen, Xian Li, Boping Wu, Bo Zhang","doi":"10.1093/hr/uhaf049","DOIUrl":null,"url":null,"abstract":"Flesh fruits are essential for human health, but pathogen infection poses a threat to fruit production and postharvest storage. The hormone salicylic acid (SA) and its metabolites, such as sugar conjugates and methyl salicylate MeSA, play a crucial role in regulating plant immune responses. However, the UDP-glycosyltransferases (UGTs) responsible for modulating SA metabolism in fruit have yet to be identified, and further investigation is needed to elucidate its involvement in fruit immune response. Here, we identified PpUGT74F2 as an enzyme with the highest transcription level in peach fruit, responsible for catalyzing the biosynthesis of SA glucoside (SAG), but not for MeSAG formation in fruit. Furthermore, infection of peach fruit with Monilinia fructicola, which causes brown rot disease, led to reduced expression of PpUGT74F2 resulting in significant decrease in SAG content and an increase in MeSA levels. Transgenic tomatoes expressing heterologous PpUGT74F2 increased susceptibility to gray mold. Interestingly, overexpressing PpUGT74F2 did not affect SA levels but dramatically reduced MeSA levels in response to pathogen infection, accompanied by significantly reduced expression of pathogen related (PR) genes in transgenic tomatoes. This study highlights that PpUGT74F2 acts as a negative regulatory factor for fruit immunity through a distinct mechanism not previously reported in plants.","PeriodicalId":13179,"journal":{"name":"Horticulture Research","volume":"14 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Horticulture Research","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/hr/uhaf049","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0

Abstract

Flesh fruits are essential for human health, but pathogen infection poses a threat to fruit production and postharvest storage. The hormone salicylic acid (SA) and its metabolites, such as sugar conjugates and methyl salicylate MeSA, play a crucial role in regulating plant immune responses. However, the UDP-glycosyltransferases (UGTs) responsible for modulating SA metabolism in fruit have yet to be identified, and further investigation is needed to elucidate its involvement in fruit immune response. Here, we identified PpUGT74F2 as an enzyme with the highest transcription level in peach fruit, responsible for catalyzing the biosynthesis of SA glucoside (SAG), but not for MeSAG formation in fruit. Furthermore, infection of peach fruit with Monilinia fructicola, which causes brown rot disease, led to reduced expression of PpUGT74F2 resulting in significant decrease in SAG content and an increase in MeSA levels. Transgenic tomatoes expressing heterologous PpUGT74F2 increased susceptibility to gray mold. Interestingly, overexpressing PpUGT74F2 did not affect SA levels but dramatically reduced MeSA levels in response to pathogen infection, accompanied by significantly reduced expression of pathogen related (PR) genes in transgenic tomatoes. This study highlights that PpUGT74F2 acts as a negative regulatory factor for fruit immunity through a distinct mechanism not previously reported in plants.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Horticulture Research
Horticulture Research Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
11.20
自引率
6.90%
发文量
367
审稿时长
20 weeks
期刊介绍: Horticulture Research, an open access journal affiliated with Nanjing Agricultural University, has achieved the prestigious ranking of number one in the Horticulture category of the Journal Citation Reports ™ from Clarivate, 2022. As a leading publication in the field, the journal is dedicated to disseminating original research articles, comprehensive reviews, insightful perspectives, thought-provoking comments, and valuable correspondence articles and letters to the editor. Its scope encompasses all vital aspects of horticultural plants and disciplines, such as biotechnology, breeding, cellular and molecular biology, evolution, genetics, inter-species interactions, physiology, and the origination and domestication of crops.
×
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