{"title":"Identification and Application of the Heptad Repeat Domain in the CPR5 Protein for Enhancing Plant Immunity.","authors":"Yuehui Zhang, Yuting Ge, Keke Sun, Leiwen Pan, Zhilin Liang, Ping Wang, Yingfan Cai, Shui Wang","doi":"10.1111/mpp.70059","DOIUrl":null,"url":null,"abstract":"<p><p>Plant resistance to pathogens can be significantly enhanced through genetic modification, thereby reducing the reliance on chemical pesticides. CONSTITUTIVE EXPRESSER OF PATHOGENESIS-RELATED GENES 5 (CPR5) serves as a key negative regulator of plant immunity. Here we explored the functional domains of the CPR5 protein with the goal of dampening its activity to bolster plant immunity. Using hexapeptide asparagine-alanine-alanine-isoleucine-arginine-serine (NAAIRS) linker-scanning analysis, we identified a heptad repeat domain (HRD) in the middle region of the CPR5 protein, which is highly conserved across the plant kingdom. The HRD is predicted to form an α-helix structure and acts as an interface for CPR5 dimerization. Intriguingly, overexpression of the HRD in Arabidopsis wild-type plants resulted in a phenotype similar to the cpr5 mutant and led to an enhancement of plant immunity, indicating that the introduced HRDs disrupt the native CPR5 dimers, thereby relieving the suppression of plant immunity. Furthermore, expression of the HRD under the control of a pathogen-inducible promoter significantly improved the resistance of cotton plants to Verticillium dahliae, a destructive wilt pathogen affecting cotton production worldwide. These findings suggest that downregulating CPR5 activity by the pathogen-inducible expression of its HRD could be a promising approach for strengthening plant immunity.</p>","PeriodicalId":18763,"journal":{"name":"Molecular plant pathology","volume":"26 2","pages":"e70059"},"PeriodicalIF":4.8000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular plant pathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/mpp.70059","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
Abstract
Plant resistance to pathogens can be significantly enhanced through genetic modification, thereby reducing the reliance on chemical pesticides. CONSTITUTIVE EXPRESSER OF PATHOGENESIS-RELATED GENES 5 (CPR5) serves as a key negative regulator of plant immunity. Here we explored the functional domains of the CPR5 protein with the goal of dampening its activity to bolster plant immunity. Using hexapeptide asparagine-alanine-alanine-isoleucine-arginine-serine (NAAIRS) linker-scanning analysis, we identified a heptad repeat domain (HRD) in the middle region of the CPR5 protein, which is highly conserved across the plant kingdom. The HRD is predicted to form an α-helix structure and acts as an interface for CPR5 dimerization. Intriguingly, overexpression of the HRD in Arabidopsis wild-type plants resulted in a phenotype similar to the cpr5 mutant and led to an enhancement of plant immunity, indicating that the introduced HRDs disrupt the native CPR5 dimers, thereby relieving the suppression of plant immunity. Furthermore, expression of the HRD under the control of a pathogen-inducible promoter significantly improved the resistance of cotton plants to Verticillium dahliae, a destructive wilt pathogen affecting cotton production worldwide. These findings suggest that downregulating CPR5 activity by the pathogen-inducible expression of its HRD could be a promising approach for strengthening 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.