{"title":"StBPA1可减弱马铃薯表面受体的激活并精细调节对细菌和卵菌病原体的免疫反应","authors":"Jie Li, Aifang Ma, Jiahan Ying, Xiuli Qin, Wenjie Liu, Wenjing Cui, Zhengyu Chen, Dongli Wang, Dongqin Chen, Zhiyuan Yin, Maofeng Jing, Guangyuan Xu, Ingo Hein, Xiangxiu Liang, Paul R.J. Birch, Daolong Dou, Xiaodan Wang","doi":"10.1016/j.devcel.2025.07.021","DOIUrl":null,"url":null,"abstract":"Plants utilize plasma-membrane-localized pattern recognition receptors (PRRs) to sense and respond to microbial infections. The downstream regulatory components have been studied extensively, but the mechanisms ensuring appropriate immune responses to diverse pathogens remain enigmatic. We report that a core regulatory component named StBPA1 (BINDING PARTNER OF ACD11) is a molecular switch that controls both anti-bacterial and anti-oomycete immunity. <ce:italic>StBPA1-</ce:italic>knockout displays dwarfed growth, enhanced pattern-triggered immunity (PTI), and broad-spectrum resistance to potato bacterial wilt and late blight diseases. StBPA1 negatively regulates the FLAGELLIN SENSING 2 (StFLS2)-BRI1-ASSOCIATED KINASE 1 (StBAK1)/SUPPRESSOR OF BIR1-1 (StSOBIR1)-StBAK1 immune complex formation and inhibits StFLS2 kinase activity to prevent constitutive immune responses. In turn, StBAK1 specifically phosphorylates StBPA1 at Thr<ce:sup loc=\"post\">193</ce:sup>/Ser<ce:sup loc=\"post\">195</ce:sup>. This modification is enhanced by flg22/INF1 perception and impairs the negative regulatory role of StBPA1, thereby ensuring proper immune signaling. These findings identify an StBPA1-PRR complex regulatory module and highlight inhibitions by StBPA1 as key mechanisms to ensure efficient yet strictly regulated immune responses against different pathogens.","PeriodicalId":11157,"journal":{"name":"Developmental cell","volume":"15 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"StBPA1 attenuates surface receptor activation and finely regulates immune responses against bacterial and oomycete pathogens in potato\",\"authors\":\"Jie Li, Aifang Ma, Jiahan Ying, Xiuli Qin, Wenjie Liu, Wenjing Cui, Zhengyu Chen, Dongli Wang, Dongqin Chen, Zhiyuan Yin, Maofeng Jing, Guangyuan Xu, Ingo Hein, Xiangxiu Liang, Paul R.J. Birch, Daolong Dou, Xiaodan Wang\",\"doi\":\"10.1016/j.devcel.2025.07.021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Plants utilize plasma-membrane-localized pattern recognition receptors (PRRs) to sense and respond to microbial infections. The downstream regulatory components have been studied extensively, but the mechanisms ensuring appropriate immune responses to diverse pathogens remain enigmatic. We report that a core regulatory component named StBPA1 (BINDING PARTNER OF ACD11) is a molecular switch that controls both anti-bacterial and anti-oomycete immunity. <ce:italic>StBPA1-</ce:italic>knockout displays dwarfed growth, enhanced pattern-triggered immunity (PTI), and broad-spectrum resistance to potato bacterial wilt and late blight diseases. StBPA1 negatively regulates the FLAGELLIN SENSING 2 (StFLS2)-BRI1-ASSOCIATED KINASE 1 (StBAK1)/SUPPRESSOR OF BIR1-1 (StSOBIR1)-StBAK1 immune complex formation and inhibits StFLS2 kinase activity to prevent constitutive immune responses. In turn, StBAK1 specifically phosphorylates StBPA1 at Thr<ce:sup loc=\\\"post\\\">193</ce:sup>/Ser<ce:sup loc=\\\"post\\\">195</ce:sup>. This modification is enhanced by flg22/INF1 perception and impairs the negative regulatory role of StBPA1, thereby ensuring proper immune signaling. These findings identify an StBPA1-PRR complex regulatory module and highlight inhibitions by StBPA1 as key mechanisms to ensure efficient yet strictly regulated immune responses against different pathogens.\",\"PeriodicalId\":11157,\"journal\":{\"name\":\"Developmental cell\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":8.7000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.devcel.2025.07.021\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.devcel.2025.07.021","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
StBPA1 attenuates surface receptor activation and finely regulates immune responses against bacterial and oomycete pathogens in potato
Plants utilize plasma-membrane-localized pattern recognition receptors (PRRs) to sense and respond to microbial infections. The downstream regulatory components have been studied extensively, but the mechanisms ensuring appropriate immune responses to diverse pathogens remain enigmatic. We report that a core regulatory component named StBPA1 (BINDING PARTNER OF ACD11) is a molecular switch that controls both anti-bacterial and anti-oomycete immunity. StBPA1-knockout displays dwarfed growth, enhanced pattern-triggered immunity (PTI), and broad-spectrum resistance to potato bacterial wilt and late blight diseases. StBPA1 negatively regulates the FLAGELLIN SENSING 2 (StFLS2)-BRI1-ASSOCIATED KINASE 1 (StBAK1)/SUPPRESSOR OF BIR1-1 (StSOBIR1)-StBAK1 immune complex formation and inhibits StFLS2 kinase activity to prevent constitutive immune responses. In turn, StBAK1 specifically phosphorylates StBPA1 at Thr193/Ser195. This modification is enhanced by flg22/INF1 perception and impairs the negative regulatory role of StBPA1, thereby ensuring proper immune signaling. These findings identify an StBPA1-PRR complex regulatory module and highlight inhibitions by StBPA1 as key mechanisms to ensure efficient yet strictly regulated immune responses against different pathogens.
期刊介绍:
Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.