Funing Meng, Dan Xiang, Ziqi Bu, Rongbin Lin, Xinyang Sun, Jiming Xu, Yunrong Wu, Yu Liu, Zhongchang Wu, Xiaorong Mo, Javier Paz-Ares, Chuanzao Mao
{"title":"h2o2介导的磷酸盐饥饿反应2的氧化促进了水稻对低磷酸盐的适应。","authors":"Funing Meng, Dan Xiang, Ziqi Bu, Rongbin Lin, Xinyang Sun, Jiming Xu, Yunrong Wu, Yu Liu, Zhongchang Wu, Xiaorong Mo, Javier Paz-Ares, Chuanzao Mao","doi":"10.1038/s41467-025-63841-0","DOIUrl":null,"url":null,"abstract":"<p><p>Phosphorus (P) is an essential macro-nutrient for plant growth and development. It is preferentially taken as inorganic phosphate (Pi). Plants have evolved elaborate mechanisms to adapt to low Pi (LP) stress through activating Pi-starvation responses. H<sub>2</sub>O<sub>2</sub> is an important signal molecule involved in plant adaptation to diverse environmental stresses. However, whether H<sub>2</sub>O<sub>2</sub> plays a role in Pi-starvation responses remains unknown. Here, we reveal that H<sub>2</sub>O<sub>2</sub> produced by the respiratory burst oxidase homologs OsRBOH-D/H facilitates phosphate uptake and utilization under LP conditions in rice. Mechanistically LP-induced H<sub>2</sub>O<sub>2</sub> promotes the oxidization of the key phosphate signaling transcription factor PHOSPHATE STARVATION RESPONSE2 (OsPHR2) at its Cys377 residue to trigger its oligomerization, sequence-specific DNA binding ability, and nuclear translocation, thereby activating Pi-starvation responses to adapt to LP conditions. Additionally, our molecular and biochemical data revealed that OsRBOH-D is a direct target gene of OsPHR2. Thus, OsPHR2 and OsRBOH-D form a positive feedback regulatory loop in which H<sub>2</sub>O<sub>2</sub> acts as a second messenger to amplify the Pi-starvation response.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"16 1","pages":"8760"},"PeriodicalIF":15.7000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"H<sub>2</sub>O<sub>2</sub>-mediated oxidation of PHOSPHATE STARVATION RESPONSE2 promotes adaptation to low phosphate in rice.\",\"authors\":\"Funing Meng, Dan Xiang, Ziqi Bu, Rongbin Lin, Xinyang Sun, Jiming Xu, Yunrong Wu, Yu Liu, Zhongchang Wu, Xiaorong Mo, Javier Paz-Ares, Chuanzao Mao\",\"doi\":\"10.1038/s41467-025-63841-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Phosphorus (P) is an essential macro-nutrient for plant growth and development. It is preferentially taken as inorganic phosphate (Pi). Plants have evolved elaborate mechanisms to adapt to low Pi (LP) stress through activating Pi-starvation responses. H<sub>2</sub>O<sub>2</sub> is an important signal molecule involved in plant adaptation to diverse environmental stresses. However, whether H<sub>2</sub>O<sub>2</sub> plays a role in Pi-starvation responses remains unknown. Here, we reveal that H<sub>2</sub>O<sub>2</sub> produced by the respiratory burst oxidase homologs OsRBOH-D/H facilitates phosphate uptake and utilization under LP conditions in rice. Mechanistically LP-induced H<sub>2</sub>O<sub>2</sub> promotes the oxidization of the key phosphate signaling transcription factor PHOSPHATE STARVATION RESPONSE2 (OsPHR2) at its Cys377 residue to trigger its oligomerization, sequence-specific DNA binding ability, and nuclear translocation, thereby activating Pi-starvation responses to adapt to LP conditions. Additionally, our molecular and biochemical data revealed that OsRBOH-D is a direct target gene of OsPHR2. Thus, OsPHR2 and OsRBOH-D form a positive feedback regulatory loop in which H<sub>2</sub>O<sub>2</sub> acts as a second messenger to amplify the Pi-starvation response.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"16 1\",\"pages\":\"8760\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-10-01\",\"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/s41467-025-63841-0\",\"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/s41467-025-63841-0","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}
H2O2-mediated oxidation of PHOSPHATE STARVATION RESPONSE2 promotes adaptation to low phosphate in rice.
Phosphorus (P) is an essential macro-nutrient for plant growth and development. It is preferentially taken as inorganic phosphate (Pi). Plants have evolved elaborate mechanisms to adapt to low Pi (LP) stress through activating Pi-starvation responses. H2O2 is an important signal molecule involved in plant adaptation to diverse environmental stresses. However, whether H2O2 plays a role in Pi-starvation responses remains unknown. Here, we reveal that H2O2 produced by the respiratory burst oxidase homologs OsRBOH-D/H facilitates phosphate uptake and utilization under LP conditions in rice. Mechanistically LP-induced H2O2 promotes the oxidization of the key phosphate signaling transcription factor PHOSPHATE STARVATION RESPONSE2 (OsPHR2) at its Cys377 residue to trigger its oligomerization, sequence-specific DNA binding ability, and nuclear translocation, thereby activating Pi-starvation responses to adapt to LP conditions. Additionally, our molecular and biochemical data revealed that OsRBOH-D is a direct target gene of OsPHR2. Thus, OsPHR2 and OsRBOH-D form a positive feedback regulatory loop in which H2O2 acts as a second messenger to amplify the Pi-starvation response.
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.