{"title":"The susceptibility factor RTP1 negatively regulates Arabidopsis immunity by interacting with the cytochrome P450 protein CYP71B3","authors":"Yushu Wei, Deqian Zong, Yaling Tang, Lehui Kong, Xianxian Gao, Xiaoxue Wang, Yingqi Zhang, Yang Yang, Xiaoyu Qiang, Weixing Shan","doi":"10.1093/plphys/kiaf284","DOIUrl":null,"url":null,"abstract":"Oomycetes, particularly Phytophthora species, cause destructive plant diseases that severely threaten sustainable crop production. Due to the loss of genotype-specific disease resistance, it is important to identify and understand immune factors that mediate plant susceptibility. Loss-of-function of the susceptibility factor Resistance To Phytophthora parasitica 1 (RTP1) leads to broad-spectrum disease resistance in Arabidopsis thaliana(Arabidopsis thaliana (L.) Heynh.). Through RNA-seq analysis, we determined that CYP71B3, encoding an uncharacterized P450 enzyme, is significantly up-regulated in rtp1 mutant plants infected with P. parasitica. Loss-of-function of CYP71B3 led to abolished pathogen-associated molecular pattern (PAMP)-triggered oxidative burst and rendered Arabidopsis more susceptible to diverse pathogens, including the oomycete P. parasitica and bacterial Pseudomonas syringae. Conversely, overexpression of CYP71B3 enhanced plant resistance and PAMP-triggered oxidative burst. CYP71B3 localized in the endoplasmic reticulum and was destabilized by interacting with RTP1 via the I-38 residue, which is essential for its immune function and P450 enzyme activity. The expression of CYP71B3 was regulated by transcription factor bZIP60, which is required for rtp1-mediated resistance to P. parasitica. Our studies indicate that RTP1 mediates plant susceptibility by destabilizing the downstream positive immune factor CYP71B3.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"51 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf284","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Oomycetes, particularly Phytophthora species, cause destructive plant diseases that severely threaten sustainable crop production. Due to the loss of genotype-specific disease resistance, it is important to identify and understand immune factors that mediate plant susceptibility. Loss-of-function of the susceptibility factor Resistance To Phytophthora parasitica 1 (RTP1) leads to broad-spectrum disease resistance in Arabidopsis thaliana(Arabidopsis thaliana (L.) Heynh.). Through RNA-seq analysis, we determined that CYP71B3, encoding an uncharacterized P450 enzyme, is significantly up-regulated in rtp1 mutant plants infected with P. parasitica. Loss-of-function of CYP71B3 led to abolished pathogen-associated molecular pattern (PAMP)-triggered oxidative burst and rendered Arabidopsis more susceptible to diverse pathogens, including the oomycete P. parasitica and bacterial Pseudomonas syringae. Conversely, overexpression of CYP71B3 enhanced plant resistance and PAMP-triggered oxidative burst. CYP71B3 localized in the endoplasmic reticulum and was destabilized by interacting with RTP1 via the I-38 residue, which is essential for its immune function and P450 enzyme activity. The expression of CYP71B3 was regulated by transcription factor bZIP60, which is required for rtp1-mediated resistance to P. parasitica. Our studies indicate that RTP1 mediates plant susceptibility by destabilizing the downstream positive immune factor CYP71B3.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.