Yupo Wu, Chuanji Zhao, Yi Zhang, Cuicui Shen, Yuanyuan Zhang, Xiong Zhang, Lixia Gao, Lingyi Zeng, Qinglin Ke, Li Qin, Fan Liu, Junyan Huang, Li Ren, Yueying Liu, Hongtao Cheng, Chaobo Tong, Qiong Hu, Xiaohui Cheng, Yangdou Wei, Shengyi Liu, Lijiang Liu
{"title":"β-1,3-葡聚糖合成酶样5的失活赋予十字花科植物对芸苔病的广谱抗性","authors":"Yupo Wu, Chuanji Zhao, Yi Zhang, Cuicui Shen, Yuanyuan Zhang, Xiong Zhang, Lixia Gao, Lingyi Zeng, Qinglin Ke, Li Qin, Fan Liu, Junyan Huang, Li Ren, Yueying Liu, Hongtao Cheng, Chaobo Tong, Qiong Hu, Xiaohui Cheng, Yangdou Wei, Shengyi Liu, Lijiang Liu","doi":"10.1038/s41588-025-02306-y","DOIUrl":null,"url":null,"abstract":"Clubroot disease, caused by the obligate intracellular rhizarian protist Plasmodiophora brassicae, is devastating to cruciferous crops worldwide. Widespread field P. brassicae pathotypes frequently overcome the pathotype-specific resistance of modern varieties, posing a challenge for durable control of this disease. Here a genome-wide association study of 3 years of data comprising field clubroot phenotyping of 244 genome-resequenced Brassica napus accessions identified a strong association of β-1,3-glucan synthase-like 5 (GSL5) with clubroot susceptibility. GSL5 was evolutionarily conserved, and inactivation of GSL5 by genome editing in Arabidopsis, B. napus, Brassica rapa and Brassica oleracea conferred broad-spectrum, high-level resistance to P. brassicae pathotypes without yield penalties in B. napus. GSL5 inactivation derepressed the jasmonic acid-mediated immunity during P. brassicae secondary infection, and this immune repression was possibly reinforced through stabilization of GSL5 by a P. brassicae effector, facilitating clubroot susceptibility. Our study provides durable resistance resources for cruciferous clubroot disease control and insights into plant resistance against intracellular eukaryotic phytopathogens. This study implicates GSL5 inactivation in high, broad-spectrum resistance to the clubroot pathogen Plasmodiophora brassicae in Arabidopsis thaliana, Brassica napus, Brassica oleracea and Brassica rapa.","PeriodicalId":18985,"journal":{"name":"Nature genetics","volume":"57 9","pages":"2302-2312"},"PeriodicalIF":29.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41588-025-02306-y.pdf","citationCount":"0","resultStr":"{\"title\":\"Inactivation of β-1,3-glucan synthase-like 5 confers broad-spectrum resistance to Plasmodiophora brassicae pathotypes in cruciferous plants\",\"authors\":\"Yupo Wu, Chuanji Zhao, Yi Zhang, Cuicui Shen, Yuanyuan Zhang, Xiong Zhang, Lixia Gao, Lingyi Zeng, Qinglin Ke, Li Qin, Fan Liu, Junyan Huang, Li Ren, Yueying Liu, Hongtao Cheng, Chaobo Tong, Qiong Hu, Xiaohui Cheng, Yangdou Wei, Shengyi Liu, Lijiang Liu\",\"doi\":\"10.1038/s41588-025-02306-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Clubroot disease, caused by the obligate intracellular rhizarian protist Plasmodiophora brassicae, is devastating to cruciferous crops worldwide. 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Inactivation of β-1,3-glucan synthase-like 5 confers broad-spectrum resistance to Plasmodiophora brassicae pathotypes in cruciferous plants
Clubroot disease, caused by the obligate intracellular rhizarian protist Plasmodiophora brassicae, is devastating to cruciferous crops worldwide. Widespread field P. brassicae pathotypes frequently overcome the pathotype-specific resistance of modern varieties, posing a challenge for durable control of this disease. Here a genome-wide association study of 3 years of data comprising field clubroot phenotyping of 244 genome-resequenced Brassica napus accessions identified a strong association of β-1,3-glucan synthase-like 5 (GSL5) with clubroot susceptibility. GSL5 was evolutionarily conserved, and inactivation of GSL5 by genome editing in Arabidopsis, B. napus, Brassica rapa and Brassica oleracea conferred broad-spectrum, high-level resistance to P. brassicae pathotypes without yield penalties in B. napus. GSL5 inactivation derepressed the jasmonic acid-mediated immunity during P. brassicae secondary infection, and this immune repression was possibly reinforced through stabilization of GSL5 by a P. brassicae effector, facilitating clubroot susceptibility. Our study provides durable resistance resources for cruciferous clubroot disease control and insights into plant resistance against intracellular eukaryotic phytopathogens. This study implicates GSL5 inactivation in high, broad-spectrum resistance to the clubroot pathogen Plasmodiophora brassicae in Arabidopsis thaliana, Brassica napus, Brassica oleracea and Brassica rapa.
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.
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