Richard Noi Morton, Lian Fleischberger, Joy Debnath, David Biermann, Susanne Mühlbauer, Ahalya Rajendran, Hans‐Henning Kunz, Julien Gronnier, Nora Gigli Bisceglia, Timo Engelsdorf
{"title":"Cell wall integrity and elicitor peptide signaling modulate jasmonic acid‐mediated camalexin production in Arabidopsis","authors":"Richard Noi Morton, Lian Fleischberger, Joy Debnath, David Biermann, Susanne Mühlbauer, Ahalya Rajendran, Hans‐Henning Kunz, Julien Gronnier, Nora Gigli Bisceglia, Timo Engelsdorf","doi":"10.1111/nph.71654","DOIUrl":null,"url":null,"abstract":"Summary <jats:list list-type=\"bullet\"> <jats:list-item> Plant cell walls constitute dynamic barriers that are essential for defense against pathogens. Beyond a structural role in blocking pathogen infection, innate mechanisms monitor cell wall integrity (CWI) in <jats:italic>Arabidopsis thaliana</jats:italic> and trigger local responses where integrity is impaired. Here, we show that THESEUS1 (THE1)‐dependent CWI signaling induces accumulation of the antimicrobial metabolite camalexin upon cell wall damage (CWD) caused by isoxaben (ISX)‐induced cellulose biosynthesis inhibition or infection with the phytopathogenic fungus <jats:italic>Colletotrichum higginsianum</jats:italic> . </jats:list-item> <jats:list-item> CWD caused by ISX alters THE1 plasma membrane nanodomain organization and involves calcium signaling components that modulate camalexin production. Induction of camalexin requires jasmonic acid (JA) signaling and JA‐dependent expression of the transcription factor MYB47. </jats:list-item> <jats:list-item> In line with its antagonistic function on CWI signaling, the plant elicitor peptide Pep3 suppresses camalexin biosynthesis downstream of THE1 by inhibiting JA‐dependent pathways. </jats:list-item> <jats:list-item> Our findings reveal a regulatory network where CWI and Pep3 signaling modulate antimicrobial defense via JA‐mediated camalexin production. This network requires input from independent CWD‐induced pathways, providing insights into how plants balance distinct defense processes in response to cell wall stress. </jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"8 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.71654","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
Summary Plant cell walls constitute dynamic barriers that are essential for defense against pathogens. Beyond a structural role in blocking pathogen infection, innate mechanisms monitor cell wall integrity (CWI) in Arabidopsis thaliana and trigger local responses where integrity is impaired. Here, we show that THESEUS1 (THE1)‐dependent CWI signaling induces accumulation of the antimicrobial metabolite camalexin upon cell wall damage (CWD) caused by isoxaben (ISX)‐induced cellulose biosynthesis inhibition or infection with the phytopathogenic fungus Colletotrichum higginsianum . CWD caused by ISX alters THE1 plasma membrane nanodomain organization and involves calcium signaling components that modulate camalexin production. Induction of camalexin requires jasmonic acid (JA) signaling and JA‐dependent expression of the transcription factor MYB47. In line with its antagonistic function on CWI signaling, the plant elicitor peptide Pep3 suppresses camalexin biosynthesis downstream of THE1 by inhibiting JA‐dependent pathways. Our findings reveal a regulatory network where CWI and Pep3 signaling modulate antimicrobial defense via JA‐mediated camalexin production. This network requires input from independent CWD‐induced pathways, providing insights into how plants balance distinct defense processes in response to cell wall stress.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.