{"title":"核孔蛋白CPR5通过鸟苷结合蛋白调控植物免疫。","authors":"Leiwen Pan, Shun Peng, Yuehui Zhang, Fenghui Xu, Xinyi Cai, Shen Liang, Qi Huang, Shilong Yu, Shui Wang","doi":"10.1111/mpp.70086","DOIUrl":null,"url":null,"abstract":"<p><p>The nuclear pore complex plays a key role in nuclear transport of immune signals. Two nucleoporins, CONSTITUTIVE EXPRESSION OF PR GENES 5 (CPR5) and GUANYLATE-BINDING PROTEIN-LIKE 3 (GBPL3), have been implicated in plant immunity. The Arabidopsis GBPL family comprises three members. While GBPL1 and GBPL3 were discovered to form an immune circuit, the role of GBPL2 remains unknown. Through genetic screening, we identified a gain-of-function mutation in GBPL2, named suppressor of cpr5 23 (scpr23), that fully suppresses the cpr5 mutant phenotype. The scpr23 function is attributed to a core amino acid residue within a nuclear export signal (NES) motif; its alteration causes a change of GBPL2 localisation from the endoplasmic reticulum to the nuclear envelope. Epistatic analysis demonstrated that knockdown of GBPL3 expression in the cpr5 scpr23 double mutant reverted its phenotype to that of the cpr5 mutant, indicating that the function conferred by scpr23 is mediated by GBPL3. We further found that GBPL2 is a counterpart of mammalian ATLASTIN-1, which belongs to a subfamily of the GBP proteins featuring transmembrane domains. Therefore, our findings reveal that the GBPL family proteins form a signalling complex that functions downstream of CPR5 to modulate plant immunity.</p>","PeriodicalId":18763,"journal":{"name":"Molecular plant pathology","volume":"26 4","pages":"e70086"},"PeriodicalIF":4.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12034427/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Nucleoporin CPR5 Modulates Plant Immunity via Guanylate-Binding Proteins.\",\"authors\":\"Leiwen Pan, Shun Peng, Yuehui Zhang, Fenghui Xu, Xinyi Cai, Shen Liang, Qi Huang, Shilong Yu, Shui Wang\",\"doi\":\"10.1111/mpp.70086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The nuclear pore complex plays a key role in nuclear transport of immune signals. Two nucleoporins, CONSTITUTIVE EXPRESSION OF PR GENES 5 (CPR5) and GUANYLATE-BINDING PROTEIN-LIKE 3 (GBPL3), have been implicated in plant immunity. The Arabidopsis GBPL family comprises three members. While GBPL1 and GBPL3 were discovered to form an immune circuit, the role of GBPL2 remains unknown. Through genetic screening, we identified a gain-of-function mutation in GBPL2, named suppressor of cpr5 23 (scpr23), that fully suppresses the cpr5 mutant phenotype. The scpr23 function is attributed to a core amino acid residue within a nuclear export signal (NES) motif; its alteration causes a change of GBPL2 localisation from the endoplasmic reticulum to the nuclear envelope. Epistatic analysis demonstrated that knockdown of GBPL3 expression in the cpr5 scpr23 double mutant reverted its phenotype to that of the cpr5 mutant, indicating that the function conferred by scpr23 is mediated by GBPL3. We further found that GBPL2 is a counterpart of mammalian ATLASTIN-1, which belongs to a subfamily of the GBP proteins featuring transmembrane domains. Therefore, our findings reveal that the GBPL family proteins form a signalling complex that functions downstream of CPR5 to modulate plant immunity.</p>\",\"PeriodicalId\":18763,\"journal\":{\"name\":\"Molecular plant pathology\",\"volume\":\"26 4\",\"pages\":\"e70086\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12034427/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular plant pathology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1111/mpp.70086\",\"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.70086","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}
The Nucleoporin CPR5 Modulates Plant Immunity via Guanylate-Binding Proteins.
The nuclear pore complex plays a key role in nuclear transport of immune signals. Two nucleoporins, CONSTITUTIVE EXPRESSION OF PR GENES 5 (CPR5) and GUANYLATE-BINDING PROTEIN-LIKE 3 (GBPL3), have been implicated in plant immunity. The Arabidopsis GBPL family comprises three members. While GBPL1 and GBPL3 were discovered to form an immune circuit, the role of GBPL2 remains unknown. Through genetic screening, we identified a gain-of-function mutation in GBPL2, named suppressor of cpr5 23 (scpr23), that fully suppresses the cpr5 mutant phenotype. The scpr23 function is attributed to a core amino acid residue within a nuclear export signal (NES) motif; its alteration causes a change of GBPL2 localisation from the endoplasmic reticulum to the nuclear envelope. Epistatic analysis demonstrated that knockdown of GBPL3 expression in the cpr5 scpr23 double mutant reverted its phenotype to that of the cpr5 mutant, indicating that the function conferred by scpr23 is mediated by GBPL3. We further found that GBPL2 is a counterpart of mammalian ATLASTIN-1, which belongs to a subfamily of the GBP proteins featuring transmembrane domains. Therefore, our findings reveal that the GBPL family proteins form a signalling complex that functions downstream of CPR5 to modulate plant immunity.
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.