Myung Geun Ji , Jin-Sung Huh , Chae Jin Lim , Gyeongik Ahn , Joon-Yung Cha , Song Yi Jeong , Gyeong-Im Shin , Aliya Alimzhan , Dae-Jin Yun , Woe-Yeon Kim
{"title":"GIGANTEA functions as a co-repressor of cold stress response with a histone-modifying complex","authors":"Myung Geun Ji , Jin-Sung Huh , Chae Jin Lim , Gyeongik Ahn , Joon-Yung Cha , Song Yi Jeong , Gyeong-Im Shin , Aliya Alimzhan , Dae-Jin Yun , Woe-Yeon Kim","doi":"10.1016/j.plaphy.2025.109801","DOIUrl":null,"url":null,"abstract":"<div><div>The circadian clock in plants is crucial for regulating stress responses, including cold tolerance. Cold stress induces the expression of <em>C-REPEAT BINDING FACTOR</em> (<em>CBF</em>) transcription factors, which activate <em>COLD-REGULATED</em> (<em>COR</em>) genes to mitigate cold-induced damage. Previously, we identified that HIGH EXPRESSION OF OSMOTICALLY RESPONSIVE GENE15 (HOS15)-HISTONE DEACETYLASE 2C (HD2C) complex regulates cold tolerance by modulating histone deacetylation on the <em>COR</em> genes. Our research reports that the circadian oscillator GIGANTEA (GI) regulates the association of histone deacetylase complex on the <em>COR</em> promoter, controlling cold tolerance. We show that GI functions downstream of HOS15, as the <em>hos15-2 gi-2</em> double mutant exhibits freezing tolerance and expression of the <em>COR</em> gene like <em>gi-2</em>. Consistent with the HOS15, GI doesn't affect <em>CBF</em> transcription, suggesting that GI involved cold stress responses through HOS15-mediated <em>COR</em> gene regulation. Moreover, GI reduces histone acetylation and CBF binding at the <em>COR15A</em> promoter under cold stress, repressing <em>COR15A</em> gene expression. We further demonstrate that GI forms a co-repressor with HOS15 and HD2C, inhibiting CBF binding and preventing <em>COR</em> gene activation under normal conditions. These findings provide insights into molecular mechanisms by which GI, HOS15, and HD2C coordinate cold stress responses, offering potential strategies for enhancing plant cold tolerance through chromatin-mediated regulation.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"223 ","pages":"Article 109801"},"PeriodicalIF":6.1000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0981942825003298","RegionNum":2,"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
The circadian clock in plants is crucial for regulating stress responses, including cold tolerance. Cold stress induces the expression of C-REPEAT BINDING FACTOR (CBF) transcription factors, which activate COLD-REGULATED (COR) genes to mitigate cold-induced damage. Previously, we identified that HIGH EXPRESSION OF OSMOTICALLY RESPONSIVE GENE15 (HOS15)-HISTONE DEACETYLASE 2C (HD2C) complex regulates cold tolerance by modulating histone deacetylation on the COR genes. Our research reports that the circadian oscillator GIGANTEA (GI) regulates the association of histone deacetylase complex on the COR promoter, controlling cold tolerance. We show that GI functions downstream of HOS15, as the hos15-2 gi-2 double mutant exhibits freezing tolerance and expression of the COR gene like gi-2. Consistent with the HOS15, GI doesn't affect CBF transcription, suggesting that GI involved cold stress responses through HOS15-mediated COR gene regulation. Moreover, GI reduces histone acetylation and CBF binding at the COR15A promoter under cold stress, repressing COR15A gene expression. We further demonstrate that GI forms a co-repressor with HOS15 and HD2C, inhibiting CBF binding and preventing COR gene activation under normal conditions. These findings provide insights into molecular mechanisms by which GI, HOS15, and HD2C coordinate cold stress responses, offering potential strategies for enhancing plant cold tolerance through chromatin-mediated regulation.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.