{"title":"Histone Methylation in Plant Responses to Abiotic Stresses.","authors":"Mei-Hui Yu, Wen-Chi Liao, Keqiang Wu","doi":"10.1093/jxb/eraf058","DOIUrl":null,"url":null,"abstract":"<p><p>Abiotic stresses, including drought, salinity, temperature fluctuations, and nutrient deficiencies, challenge plant growth and productivity, requiring adaptive mechanisms for survival. Histone modifications, especially histone methylation, participate in gene expression regulation in response to these stresses. Notably, bivalent H3K4me3-H3K27me3 modifications play a central role in fine-tuning stress-responsive genes, allowing plants adapt to environmental changes. Recent studies have highlighted the dynamic switching of these bivalent chromatin marks at specific loci during stress, facilitating plant acclimatization to adverse environments. This review focuses on the four major histone H3 methylation modifications-H3K4, H3K9, H3K27, and H3K36-examining the roles of the associated methyltransferases and demethylases in mediating histone methylation dynamics. We synthesize recent findings on how these modifications regulate plant responses to various abiotic stresses, such as drought, salinity, heat, light stress, heavy metal exposure, and nutrient stress. By exploring these molecular mechanisms, we aim to deepen the understanding of how histone methylation shapes plant stress responses at both transcriptional and epigenetic levels. Furthermore, we also discuss the functional interaction of histone methylation with histone acetylation. These insights are critical for advancing breeding strategies aimed at improving plant tolerance to environmental stressors, ensuring food security, and supporting sustainable agricultural practices amid climate change.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/eraf058","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
Abiotic stresses, including drought, salinity, temperature fluctuations, and nutrient deficiencies, challenge plant growth and productivity, requiring adaptive mechanisms for survival. Histone modifications, especially histone methylation, participate in gene expression regulation in response to these stresses. Notably, bivalent H3K4me3-H3K27me3 modifications play a central role in fine-tuning stress-responsive genes, allowing plants adapt to environmental changes. Recent studies have highlighted the dynamic switching of these bivalent chromatin marks at specific loci during stress, facilitating plant acclimatization to adverse environments. This review focuses on the four major histone H3 methylation modifications-H3K4, H3K9, H3K27, and H3K36-examining the roles of the associated methyltransferases and demethylases in mediating histone methylation dynamics. We synthesize recent findings on how these modifications regulate plant responses to various abiotic stresses, such as drought, salinity, heat, light stress, heavy metal exposure, and nutrient stress. By exploring these molecular mechanisms, we aim to deepen the understanding of how histone methylation shapes plant stress responses at both transcriptional and epigenetic levels. Furthermore, we also discuss the functional interaction of histone methylation with histone acetylation. These insights are critical for advancing breeding strategies aimed at improving plant tolerance to environmental stressors, ensuring food security, and supporting sustainable agricultural practices amid climate change.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.