{"title":"Epitranscriptomic Control of Drought Tolerance in Rice: The Role of RNA Methylation.","authors":"Xiaoru Fan, Yong Zhang, Pengyuan Gu, Misbah Naz","doi":"10.3390/plants14132002","DOIUrl":null,"url":null,"abstract":"<p><p>Drought stress is a predominant abiotic constraint adversely affecting global rice (<i>Oryza sativa</i>) production and threatening food security. While the transcriptional and post-transcriptional regulation of drought-responsive pathways has been widely investigated, the emerging field of epitranscriptomics, particularly RNA chemical modifications such as N6-methyladenosine (m<sup>6</sup>A), adds a new dimension to gene regulation under stress. The most prevalent internal modification in eukaryotic messenger RNA influences RNA metabolism by interacting dynamically with enzymes that add, remove, or recognize the modification. Recent studies in rice reveal that m<sup>6</sup>A deposition is not static but dynamically regulated in response to water-deficit conditions, influencing transcript stability, splicing, nuclear export, and translation efficiency of key drought-responsive genes. This review critically synthesizes current findings on the distribution and functional implications of m<sup>6</sup>A and other epitranscriptomic marks (e.g., 5-methylcytosine [m<sup>5</sup>C], <i>pseudouridine</i> [Ψ]) in modulating rice responses to drought. We discuss the regulatory circuitry involving m<sup>6</sup>A effectors such as <i>OsMTA</i>, <i>OsFIP37</i>, and <i>YTH</i> domain proteins and their integration with known drought-signaling pathways including ABA and reactive oxygen species (ROS) cascades. We also highlight emerging high-resolution technologies such as m<sup>6</sup>A-seq, direct RNA sequencing, and nanopore-based detection that facilitate epitranscriptomic profiling in rice. Finally, we propose future directions for translating epitranscriptomic knowledge into crop improvement, including <i>CRISPR</i>/<i>Cas</i>-based modulation of RNA modification machinery to enhance drought tolerance.</p>","PeriodicalId":56267,"journal":{"name":"Plants-Basel","volume":"14 13","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12252055/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plants-Basel","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/plants14132002","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
Drought stress is a predominant abiotic constraint adversely affecting global rice (Oryza sativa) production and threatening food security. While the transcriptional and post-transcriptional regulation of drought-responsive pathways has been widely investigated, the emerging field of epitranscriptomics, particularly RNA chemical modifications such as N6-methyladenosine (m6A), adds a new dimension to gene regulation under stress. The most prevalent internal modification in eukaryotic messenger RNA influences RNA metabolism by interacting dynamically with enzymes that add, remove, or recognize the modification. Recent studies in rice reveal that m6A deposition is not static but dynamically regulated in response to water-deficit conditions, influencing transcript stability, splicing, nuclear export, and translation efficiency of key drought-responsive genes. This review critically synthesizes current findings on the distribution and functional implications of m6A and other epitranscriptomic marks (e.g., 5-methylcytosine [m5C], pseudouridine [Ψ]) in modulating rice responses to drought. We discuss the regulatory circuitry involving m6A effectors such as OsMTA, OsFIP37, and YTH domain proteins and their integration with known drought-signaling pathways including ABA and reactive oxygen species (ROS) cascades. We also highlight emerging high-resolution technologies such as m6A-seq, direct RNA sequencing, and nanopore-based detection that facilitate epitranscriptomic profiling in rice. Finally, we propose future directions for translating epitranscriptomic knowledge into crop improvement, including CRISPR/Cas-based modulation of RNA modification machinery to enhance drought tolerance.
Plants-BaselAgricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
6.50
自引率
11.10%
发文量
2923
审稿时长
15.4 days
期刊介绍:
Plants (ISSN 2223-7747), is an international and multidisciplinary scientific open access journal that covers all key areas of plant science. It publishes review articles, regular research articles, communications, and short notes in the fields of structural, functional and experimental botany. In addition to fundamental disciplines such as morphology, systematics, physiology and ecology of plants, the journal welcomes all types of articles in the field of applied plant science.