{"title":"The OST1-HOS1-HAT1 module regulates cold response in Arabidopsis thaliana","authors":"Xinke Kang, Fan Wei, Shuli Chai, Sihan Peng, Bingyao Huang, Qing Han, Tianyue Zhao, Peiyi Zhang, Yuang Tian, Ran Xia, Honghui Lin, Dawei Zhang","doi":"10.1111/nph.70189","DOIUrl":null,"url":null,"abstract":"<p>\n</p><ul>\n<li>Plants have evolved sophisticated strategies to cope with various environmental stresses. Recent studies have provided insights into the mechanisms of rapid cold stress response through key components including OST1, ICE1, HOS1, and CBFs. However, the mechanisms by which plants modulate the intensity of their cold tolerance in response to fluctuating temperatures remain largely unexplored.</li>\n<li>In this study, we employed a multidisciplinary approach integrating molecular biology, plant physiology, and genetic methodologies to comprehensively decipher the molecular mechanisms by which HAT1 regulates cold stress responses in plants and further unraveled its cold-dependent posttranslational modification network.</li>\n<li>We found that under normal conditions, HAT1 acts as a repressor of cold-induced expression of <i>CBF</i> and <i>COR</i> genes, attenuating the cold response. When plants are exposed to cold stress, cold triggers OST1 to phosphorylate HAT1 and facilitates its interaction with HOS1, which subsequently induces ubiquitination and degradation of HAT1. This process alleviates repression of the <i>CBF</i> and <i>COR</i> genes by HAT1 and activates the cold stress response.</li>\n<li>Thus, our results reveal that HAT1 acts as a brake to prevent excessive cold stress response. The OST1-HOS1 module regulates HAT1 protein stability, allowing plants to dynamically balance growth and cold tolerance in response to environmental signals.</li>\n</ul><p></p>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"36 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-05-07","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.70189","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
Plants have evolved sophisticated strategies to cope with various environmental stresses. Recent studies have provided insights into the mechanisms of rapid cold stress response through key components including OST1, ICE1, HOS1, and CBFs. However, the mechanisms by which plants modulate the intensity of their cold tolerance in response to fluctuating temperatures remain largely unexplored.
In this study, we employed a multidisciplinary approach integrating molecular biology, plant physiology, and genetic methodologies to comprehensively decipher the molecular mechanisms by which HAT1 regulates cold stress responses in plants and further unraveled its cold-dependent posttranslational modification network.
We found that under normal conditions, HAT1 acts as a repressor of cold-induced expression of CBF and COR genes, attenuating the cold response. When plants are exposed to cold stress, cold triggers OST1 to phosphorylate HAT1 and facilitates its interaction with HOS1, which subsequently induces ubiquitination and degradation of HAT1. This process alleviates repression of the CBF and COR genes by HAT1 and activates the cold stress response.
Thus, our results reveal that HAT1 acts as a brake to prevent excessive cold stress response. The OST1-HOS1 module regulates HAT1 protein stability, allowing plants to dynamically balance growth and cold tolerance in response to environmental signals.
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.