{"title":"Arabidopsis STN7/STN8 alleviates oxidative damages via different regulatory patterns under drought stress","authors":"Hao-Tian Mao, Ying Qin, Lun-Xing Chen, Yi-Cheng Zhang, Fu-Yun Wang, Shu Yuan, Shozeb Haider, Yang-Er Chen","doi":"10.1111/tpj.71101","DOIUrl":null,"url":null,"abstract":"<p>STN7 and STN8 kinases phosphorylate several proteins of the photosynthetic apparatus in response to changes in environmental conditions. Phosphorylation is linked to the dynamic arrangement of both the 3D structure of the thylakoid membrane and thylakoid protein complexes, thereby controlling excitation energy transfer between photosystems and the repair cycle of photosystem II (PSII). However, mutants with phosphorylation of PSII core proteins show only minor changes compared with the wild-type (WT) under conditions tested so far, and thus the physiological significance of reversible thylakoid protein phosphorylation by STN8 remains largely unresolved. In this study, we examined the impact of STN7 and STN8 on osmotic stress and consequent changes in the structure of the thylakoid membrane in <i>Arabidopsis thaliana</i> using physiological, cellular, and biochemical assays. Our results demonstrate that Arabidopsis plants lacking STN7 or STN8 exhibited slow growth and impaired regulation of excitation energy transfer, as well as low photosynthetic efficiency, excessive accumulation of ROS, and more severe cell death in response to osmotic stress compared with the WT. Clear effects of osmotic stress were observed in both <i>stn7</i> and <i>stn8</i> mutants but were more pronounced in the <i>stn7stn8</i> double mutant. Our data strongly suggest that phosphorylation of the PSII reaction center proteins, regulated by STN8, is important for maintaining the functional balance of the photosynthetic apparatus under osmotic stress-induced changes in the thylakoid membrane and thus protects it from oxidative stress.</p>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"127 5","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/tpj.71101","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.71101","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
STN7 and STN8 kinases phosphorylate several proteins of the photosynthetic apparatus in response to changes in environmental conditions. Phosphorylation is linked to the dynamic arrangement of both the 3D structure of the thylakoid membrane and thylakoid protein complexes, thereby controlling excitation energy transfer between photosystems and the repair cycle of photosystem II (PSII). However, mutants with phosphorylation of PSII core proteins show only minor changes compared with the wild-type (WT) under conditions tested so far, and thus the physiological significance of reversible thylakoid protein phosphorylation by STN8 remains largely unresolved. In this study, we examined the impact of STN7 and STN8 on osmotic stress and consequent changes in the structure of the thylakoid membrane in Arabidopsis thaliana using physiological, cellular, and biochemical assays. Our results demonstrate that Arabidopsis plants lacking STN7 or STN8 exhibited slow growth and impaired regulation of excitation energy transfer, as well as low photosynthetic efficiency, excessive accumulation of ROS, and more severe cell death in response to osmotic stress compared with the WT. Clear effects of osmotic stress were observed in both stn7 and stn8 mutants but were more pronounced in the stn7stn8 double mutant. Our data strongly suggest that phosphorylation of the PSII reaction center proteins, regulated by STN8, is important for maintaining the functional balance of the photosynthetic apparatus under osmotic stress-induced changes in the thylakoid membrane and thus protects it from oxidative stress.
期刊介绍:
Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community.
Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.