{"title":"一种直接蛋白重定向细胞外萜类代谢,以防御生物挑战。","authors":"Jia-Ling Lin,Wen-Kai Wu,Gui-Bin Nie,Jian-Xu Li,Xin Fang,Yin-Guo Sheng,Meng-Meng Wang,Qi-Yue Zheng,Xiao-Xiang Guo,Jia-Fa Huang,Li-Ying Ma,Ling-Jian Wang,Jia-Xin Liu,Shan-Shan Wang,Baofu Xu,Yiqun Gao,Yan Li,Dong Wang,Cathie Martin,Xiao-Ya Chen,Jin-Quan Huang","doi":"10.1038/s41467-025-64323-z","DOIUrl":null,"url":null,"abstract":"Plants have evolved an extensive repertoire of specialized metabolites to adapt to complex environmental changes. Here, we identify two paralogous dirigent proteins (DPs) in cotton that serve as gatekeepers of extracellular terpenoid phytoalexin production in green organs, directing the transition of hemigossypol away from gossypol synthesis toward a hydroxylation pathway that leads to the biosynthesis of highly toxic hemigossypolone and heliocides. Under oxidative conditions, these proteins function synergistically with aldo-keto reductases to catalyze the hydroxylation of hemigossypol, followed by spontaneous oxidation that yields hemigossypolone, revealing a noncanonical role for aldo-keto reductases in extracellular terpenoid metabolism. Notably, mutants lacking these dirigent proteins produce gossypol but are devoid of hemigossypolone and heliocides in green organs exhibit heightened susceptibility to multiple biotic stresses, underscoring the enhanced protective role of these metabolites. This study describes a DPs-mediated mechanism of extracellular hydroxylation and highlights the potential ecological advantages of redirecting specialized metabolism extracellularly for enhanced defense against varying types of pathogens and herbivores.","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"12 1","pages":"9270"},"PeriodicalIF":15.7000,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A dirigent protein redirects extracellular terpenoid metabolism for defense against biotic challenges.\",\"authors\":\"Jia-Ling Lin,Wen-Kai Wu,Gui-Bin Nie,Jian-Xu Li,Xin Fang,Yin-Guo Sheng,Meng-Meng Wang,Qi-Yue Zheng,Xiao-Xiang Guo,Jia-Fa Huang,Li-Ying Ma,Ling-Jian Wang,Jia-Xin Liu,Shan-Shan Wang,Baofu Xu,Yiqun Gao,Yan Li,Dong Wang,Cathie Martin,Xiao-Ya Chen,Jin-Quan Huang\",\"doi\":\"10.1038/s41467-025-64323-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Plants have evolved an extensive repertoire of specialized metabolites to adapt to complex environmental changes. Here, we identify two paralogous dirigent proteins (DPs) in cotton that serve as gatekeepers of extracellular terpenoid phytoalexin production in green organs, directing the transition of hemigossypol away from gossypol synthesis toward a hydroxylation pathway that leads to the biosynthesis of highly toxic hemigossypolone and heliocides. Under oxidative conditions, these proteins function synergistically with aldo-keto reductases to catalyze the hydroxylation of hemigossypol, followed by spontaneous oxidation that yields hemigossypolone, revealing a noncanonical role for aldo-keto reductases in extracellular terpenoid metabolism. Notably, mutants lacking these dirigent proteins produce gossypol but are devoid of hemigossypolone and heliocides in green organs exhibit heightened susceptibility to multiple biotic stresses, underscoring the enhanced protective role of these metabolites. This study describes a DPs-mediated mechanism of extracellular hydroxylation and highlights the potential ecological advantages of redirecting specialized metabolism extracellularly for enhanced defense against varying types of pathogens and herbivores.\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"12 1\",\"pages\":\"9270\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-64323-z\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-64323-z","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
A dirigent protein redirects extracellular terpenoid metabolism for defense against biotic challenges.
Plants have evolved an extensive repertoire of specialized metabolites to adapt to complex environmental changes. Here, we identify two paralogous dirigent proteins (DPs) in cotton that serve as gatekeepers of extracellular terpenoid phytoalexin production in green organs, directing the transition of hemigossypol away from gossypol synthesis toward a hydroxylation pathway that leads to the biosynthesis of highly toxic hemigossypolone and heliocides. Under oxidative conditions, these proteins function synergistically with aldo-keto reductases to catalyze the hydroxylation of hemigossypol, followed by spontaneous oxidation that yields hemigossypolone, revealing a noncanonical role for aldo-keto reductases in extracellular terpenoid metabolism. Notably, mutants lacking these dirigent proteins produce gossypol but are devoid of hemigossypolone and heliocides in green organs exhibit heightened susceptibility to multiple biotic stresses, underscoring the enhanced protective role of these metabolites. This study describes a DPs-mediated mechanism of extracellular hydroxylation and highlights the potential ecological advantages of redirecting specialized metabolism extracellularly for enhanced defense against varying types of pathogens and herbivores.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.