Yingchun Han, Qianfeng Hu, Nuo Gong, Huimin Yan, Najeeb Ullah Khan, Yanxiu Du, Hongzheng Sun, Quanzhi Zhao, Wanxi Peng, Zichao Li, Zhanying Zhang, Junzhou Li
{"title":"Natural variation in MORE GRAINS 1 regulates grain number and grain weight in rice","authors":"Yingchun Han, Qianfeng Hu, Nuo Gong, Huimin Yan, Najeeb Ullah Khan, Yanxiu Du, Hongzheng Sun, Quanzhi Zhao, Wanxi Peng, Zichao Li, Zhanying Zhang, Junzhou Li","doi":"10.1111/jipb.13674","DOIUrl":null,"url":null,"abstract":"<p>Grain yield is determined mainly by grain number and grain weight. In this study, we identified and characterized <i>MORE GRAINS1</i> (<i>MOG1</i>), a gene associated with grain number and grain weight in rice (<i>Oryza sativa</i> L.), through map-based cloning. Overexpression of <i>MOG1</i> increased grain yield by 18.6%–22.3% under field conditions. We determined that MOG1, a bHLH transcription factor, interacts with OsbHLH107 and directly activates the expression of <i>LONELY GUY</i> (<i>LOG</i>), which encodes a cytokinin-activating enzyme and the cell expansion gene <i>EXPANSIN-LIKE1</i> (<i>EXPLA1</i>), positively regulating grain number per panicle and grain weight. Natural variations in the promoter and coding regions of <i>MOG1</i> between Hap-LNW and Hap-HNW alleles resulted in changes in <i>MOG1</i> expression level and transcriptional activation, leading to functional differences. Haplotype analysis revealed that Hap-HNW, which results in a greater number and heavier grains, has undergone strong selection but has been poorly utilized in modern lowland rice breeding. In summary, the MOG1–OsbHLH107 complex activates <i>LOG</i> and <i>EXPLA1</i> expression to promote cell expansion and division of young panicles through the cytokinin pathway, thereby increasing grain number and grain weight. These findings suggest that Hap-HNW could be used in strategies to breed high-yielding temperate <i>japonica</i> lowland rice.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":"66 7","pages":"1440-1458"},"PeriodicalIF":9.3000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jipb.13674","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jipb.13674","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Grain yield is determined mainly by grain number and grain weight. In this study, we identified and characterized MORE GRAINS1 (MOG1), a gene associated with grain number and grain weight in rice (Oryza sativa L.), through map-based cloning. Overexpression of MOG1 increased grain yield by 18.6%–22.3% under field conditions. We determined that MOG1, a bHLH transcription factor, interacts with OsbHLH107 and directly activates the expression of LONELY GUY (LOG), which encodes a cytokinin-activating enzyme and the cell expansion gene EXPANSIN-LIKE1 (EXPLA1), positively regulating grain number per panicle and grain weight. Natural variations in the promoter and coding regions of MOG1 between Hap-LNW and Hap-HNW alleles resulted in changes in MOG1 expression level and transcriptional activation, leading to functional differences. Haplotype analysis revealed that Hap-HNW, which results in a greater number and heavier grains, has undergone strong selection but has been poorly utilized in modern lowland rice breeding. In summary, the MOG1–OsbHLH107 complex activates LOG and EXPLA1 expression to promote cell expansion and division of young panicles through the cytokinin pathway, thereby increasing grain number and grain weight. These findings suggest that Hap-HNW could be used in strategies to breed high-yielding temperate japonica lowland rice.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.