{"title":"The long noncoding RNA VIVIpary promotes seed dormancy release and pre-harvest sprouting through chromatin remodeling in rice.","authors":"Lu Yang, Yu Cheng, Chao Yuan, Yan-Fei Zhou, Qiao-Juan Huang, Wen-Long Zhao, Rui-Rui He, Jie Jiang, Yi-Chao Qin, Zheng-Tong Chen, Yu-Chan Zhang, Meng-Qi Lei, Jian-Ping Lian, Yue-Qin Chen","doi":"10.1016/j.molp.2025.04.010","DOIUrl":null,"url":null,"abstract":"<p><p>Seed dormancy enables seeds to remain dormant until the environmental conditions are ideal for germination. Understanding the molecular mechanisms that underlie seed dormancy is essential for improving grain quality and preventing pre-harvest sprouting (PHS), a major challenge in global agriculture. Here, we address how long noncoding RNAs (lncRNAs) contribute to the regulation of seed dormancy in rice (Oryza sativa). We identified an lncRNA, VIVIpary, that is specifically expressed in embryos and is associated with shortened seed dormancy. VIVIpary exhibits higher expression in a PHS-sensitive variety, and its overexpression induces PHS, whereas its knockdown delays germination. Mechanistically, VIVIpary promotes the release of seed dormancy by regulating abscisic acid (ABA) signaling. VIVIpary serves as a spatial organizer that shapes chromatin architecture by directly binding to the chromatin adaptor protein OsMSI1 and enhancing its interaction with the histone deacetylase OsHDAC1, thereby reducing chromatin accessibility and fine-tuning ABA signaling. VIVIpary is differentially expressed between wild and cultivated rice, with higher expression in japonica rice, suggesting that it was a target of selection during rice domestication. Together, our findings reveal a domestication-associated lncRNA that modulates ABA signaling and chromatin architecture to regulate seed dormancy and PHS in rice, providing a potential target for improvement of rice agronomic traits.</p>","PeriodicalId":19012,"journal":{"name":"Molecular Plant","volume":" ","pages":"978-994"},"PeriodicalIF":17.1000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.molp.2025.04.010","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Seed dormancy enables seeds to remain dormant until the environmental conditions are ideal for germination. Understanding the molecular mechanisms that underlie seed dormancy is essential for improving grain quality and preventing pre-harvest sprouting (PHS), a major challenge in global agriculture. Here, we address how long noncoding RNAs (lncRNAs) contribute to the regulation of seed dormancy in rice (Oryza sativa). We identified an lncRNA, VIVIpary, that is specifically expressed in embryos and is associated with shortened seed dormancy. VIVIpary exhibits higher expression in a PHS-sensitive variety, and its overexpression induces PHS, whereas its knockdown delays germination. Mechanistically, VIVIpary promotes the release of seed dormancy by regulating abscisic acid (ABA) signaling. VIVIpary serves as a spatial organizer that shapes chromatin architecture by directly binding to the chromatin adaptor protein OsMSI1 and enhancing its interaction with the histone deacetylase OsHDAC1, thereby reducing chromatin accessibility and fine-tuning ABA signaling. VIVIpary is differentially expressed between wild and cultivated rice, with higher expression in japonica rice, suggesting that it was a target of selection during rice domestication. Together, our findings reveal a domestication-associated lncRNA that modulates ABA signaling and chromatin architecture to regulate seed dormancy and PHS in rice, providing a potential target for improvement of rice agronomic traits.
期刊介绍:
Molecular Plant is dedicated to serving the plant science community by publishing novel and exciting findings with high significance in plant biology. The journal focuses broadly on cellular biology, physiology, biochemistry, molecular biology, genetics, development, plant-microbe interaction, genomics, bioinformatics, and molecular evolution.
Molecular Plant publishes original research articles, reviews, Correspondence, and Spotlights on the most important developments in plant biology.