Coordinated function of paired NLRs confers Yr84-mediated stripe rust resistance in wheat

IF 31.7 1区 生物学 Q1 GENETICS & HEREDITY
Valentyna Klymiuk, Krystalee Wiebe, Harmeet Singh Chawla, Jennifer Ens, Rajagopal Subramaniam, Curtis J. Pozniak
{"title":"Coordinated function of paired NLRs confers Yr84-mediated stripe rust resistance in wheat","authors":"Valentyna Klymiuk, Krystalee Wiebe, Harmeet Singh Chawla, Jennifer Ens, Rajagopal Subramaniam, Curtis J. Pozniak","doi":"10.1038/s41588-025-02203-4","DOIUrl":null,"url":null,"abstract":"Cloning of resistance genes expands our understanding of their function and facilitates their deployment in breeding. Here we report the cloning of two genes from wild emmer wheat (Triticum turgidum ssp. dicoccoides) underlying Yr84-mediated stripe rust resistance using a combination of fine mapping, long-read sequencing and mutation-induced functional validation. In contrast to all previously cloned stripe rust genes, the incompletely dominant Yr84 phenotype is conferred through the coordinated function of paired nucleotide-binding leucine-rich repeat (NLR) genes CNL and NL. We reason that based on their genomic organization, annotation, expression profiles and predicted protein structure, CNL functions as a sensor NLR, responsible for effector recognition, and NL acts as a helper NLR, initiating downstream resistance cascades. Both the CNL and NL lack an integrated domain(s) previously implicated in effector recognition by paired NLRs; therefore, these findings contribute insights into the structure and molecular mechanisms of the function of plant paired NLRs. The study reports the cloning of paired NLR genes CNL and NL from wild emmer wheat and demonstrates their coordinated function in conferring Yr84-mediated wheat stripe rust resistance.","PeriodicalId":18985,"journal":{"name":"Nature genetics","volume":"57 6","pages":"1535-1542"},"PeriodicalIF":31.7000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature genetics","FirstCategoryId":"99","ListUrlMain":"https://www.nature.com/articles/s41588-025-02203-4","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Cloning of resistance genes expands our understanding of their function and facilitates their deployment in breeding. Here we report the cloning of two genes from wild emmer wheat (Triticum turgidum ssp. dicoccoides) underlying Yr84-mediated stripe rust resistance using a combination of fine mapping, long-read sequencing and mutation-induced functional validation. In contrast to all previously cloned stripe rust genes, the incompletely dominant Yr84 phenotype is conferred through the coordinated function of paired nucleotide-binding leucine-rich repeat (NLR) genes CNL and NL. We reason that based on their genomic organization, annotation, expression profiles and predicted protein structure, CNL functions as a sensor NLR, responsible for effector recognition, and NL acts as a helper NLR, initiating downstream resistance cascades. Both the CNL and NL lack an integrated domain(s) previously implicated in effector recognition by paired NLRs; therefore, these findings contribute insights into the structure and molecular mechanisms of the function of plant paired NLRs. The study reports the cloning of paired NLR genes CNL and NL from wild emmer wheat and demonstrates their coordinated function in conferring Yr84-mediated wheat stripe rust resistance.

Abstract Image

配对NLRs的协同作用决定了yr84介导的小麦抗条锈病能力
抗性基因的克隆扩展了我们对其功能的理解,并促进了它们在育种中的应用。本文报道了野生二粒小麦(Triticum turgidum ssp)的两个基因的克隆。利用精细定位、长读测序和突变诱导的功能验证相结合的方法,对yr84介导的条纹锈病抗性进行了研究。与之前克隆的所有条纹锈病基因相比,不完全显性的Yr84表型是通过配对的核苷酸结合富亮氨酸重复序列(NLR)基因CNL和NL的协调功能赋予的。我们认为,基于它们的基因组组织、注释、表达谱和预测的蛋白质结构,CNL作为传感器NLR,负责效应物识别,而NL作为辅助NLR,启动下游的抗性级联。CNL和NL都缺乏一个集成域(s),先前涉及到成对nlr的效应识别;因此,这些发现有助于深入了解植物配对NLRs的结构和功能的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
×
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