拟南芥对交替稻瘟菌感染防御反应的新调控因子及其上位网络。

IF 4.8 1区 农林科学 Q1 PLANT SCIENCES
Qi Zeng, Xifan Liu, Xuemei Yan, Jiahao Zhang, Chao Li, Chengtai Yan, Yanfeng Zhang, Daniel Kliebenstein, Baohua Li
{"title":"拟南芥对交替稻瘟菌感染防御反应的新调控因子及其上位网络。","authors":"Qi Zeng, Xifan Liu, Xuemei Yan, Jiahao Zhang, Chao Li, Chengtai Yan, Yanfeng Zhang, Daniel Kliebenstein, Baohua Li","doi":"10.1111/mpp.70058","DOIUrl":null,"url":null,"abstract":"<p><p>Necrotrophic pathogens cause serious threats to agricultural crops, and understanding the resistance genes and their genetic networks is key to breeding new plant cultivars with better resistance traits. Although Alternaria alternata causes black spot in important leafy brassica vegetables, and leads to significant loss of yield and food quality, little is known about plant-A. alternata interactions. In this study, we used a unique and large collection of single, double and triple mutant lines of defence metabolite regulators in Arabidopsis to explore how these transcription factors and their epistatic networks may influence A. alternata infections. This identified nine novel regulators and 20 pairs of epistatic interactions that modulate Arabidopsis plants' defence responses to A. alternata infection. We further showed that the glucosinolate 4-methoxy-indol-3-ylmethyl is the only glucosinolate consistently responsive to A. alternata infection in Col-0 ecotype. With the further exploration of the regulators and the genetic networks on modulating the accumulation of glucosinolates under A. alternata infection, an inverted triangle regulatory model was proposed for Arabidopsis plants' defence responses at a metabolic level and a phenotypic level.</p>","PeriodicalId":18763,"journal":{"name":"Molecular plant pathology","volume":"26 2","pages":"e70058"},"PeriodicalIF":4.8000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11788323/pdf/","citationCount":"0","resultStr":"{\"title\":\"Novel Regulators and Their Epistatic Networks in Arabidopsis' Defence Responses to Alternaria alternata Infection.\",\"authors\":\"Qi Zeng, Xifan Liu, Xuemei Yan, Jiahao Zhang, Chao Li, Chengtai Yan, Yanfeng Zhang, Daniel Kliebenstein, Baohua Li\",\"doi\":\"10.1111/mpp.70058\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Necrotrophic pathogens cause serious threats to agricultural crops, and understanding the resistance genes and their genetic networks is key to breeding new plant cultivars with better resistance traits. Although Alternaria alternata causes black spot in important leafy brassica vegetables, and leads to significant loss of yield and food quality, little is known about plant-A. alternata interactions. In this study, we used a unique and large collection of single, double and triple mutant lines of defence metabolite regulators in Arabidopsis to explore how these transcription factors and their epistatic networks may influence A. alternata infections. This identified nine novel regulators and 20 pairs of epistatic interactions that modulate Arabidopsis plants' defence responses to A. alternata infection. We further showed that the glucosinolate 4-methoxy-indol-3-ylmethyl is the only glucosinolate consistently responsive to A. alternata infection in Col-0 ecotype. With the further exploration of the regulators and the genetic networks on modulating the accumulation of glucosinolates under A. alternata infection, an inverted triangle regulatory model was proposed for Arabidopsis plants' defence responses at a metabolic level and a phenotypic level.</p>\",\"PeriodicalId\":18763,\"journal\":{\"name\":\"Molecular plant pathology\",\"volume\":\"26 2\",\"pages\":\"e70058\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11788323/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular plant pathology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1111/mpp.70058\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular plant pathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/mpp.70058","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

坏死性致病菌对农作物造成严重威胁,了解其抗性基因及其遗传网络是培育具有较好抗性性状的植物新品种的关键。虽然互交霉属(Alternaria alternata)在重要的绿叶芸苔类蔬菜中引起黑斑病,并导致重大的产量和食品质量损失,但对植物a知之甚少。alternata交互。在这项研究中,我们使用了大量独特的拟南芥单突变、双突变和三突变防御代谢物调节剂来探索这些转录因子及其epistatic网络如何影响草属植物的感染。本研究确定了9个新的调控因子和20对上位相互作用,这些相互作用调节拟南芥植物对a.m alternata感染的防御反应。我们进一步发现,4-甲氧基吲哚-3-甲基硫代葡萄糖苷是col0生态型中唯一对异花蒿感染持续响应的硫代葡萄糖苷。随着对拟南芥侵染条件下硫代葡萄糖苷积累调控机制和遗传网络的进一步探索,本文提出了拟南芥植物防御反应在代谢水平和表型水平上的倒三角调控模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Regulators and Their Epistatic Networks in Arabidopsis' Defence Responses to Alternaria alternata Infection.

Necrotrophic pathogens cause serious threats to agricultural crops, and understanding the resistance genes and their genetic networks is key to breeding new plant cultivars with better resistance traits. Although Alternaria alternata causes black spot in important leafy brassica vegetables, and leads to significant loss of yield and food quality, little is known about plant-A. alternata interactions. In this study, we used a unique and large collection of single, double and triple mutant lines of defence metabolite regulators in Arabidopsis to explore how these transcription factors and their epistatic networks may influence A. alternata infections. This identified nine novel regulators and 20 pairs of epistatic interactions that modulate Arabidopsis plants' defence responses to A. alternata infection. We further showed that the glucosinolate 4-methoxy-indol-3-ylmethyl is the only glucosinolate consistently responsive to A. alternata infection in Col-0 ecotype. With the further exploration of the regulators and the genetic networks on modulating the accumulation of glucosinolates under A. alternata infection, an inverted triangle regulatory model was proposed for Arabidopsis plants' defence responses at a metabolic level and a phenotypic level.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular plant pathology
Molecular plant pathology 生物-植物科学
CiteScore
9.40
自引率
4.10%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Molecular Plant Pathology is now an open access journal. Authors pay an article processing charge to publish in the journal and all articles will be freely available to anyone. BSPP members will be granted a 20% discount on article charges. The Editorial focus and policy of the journal has not be changed and the editorial team will continue to apply the same rigorous standards of peer review and acceptance criteria.
×
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:604180095
Book学术官方微信