Fengcheng Li, Lian Wu, Xiang Li, Yanan Chai, Nan Ruan, Ye Wang, Na Xu, Zhiwen Yu, Xiaoche Wang, Hao Chen, Jiahao Lu, Hai Xu, Zhengjin Xu, Wenfu Chen, Quan Xu
{"title":"Dissecting the molecular basis of the ultra-large grain formation in rice","authors":"Fengcheng Li, Lian Wu, Xiang Li, Yanan Chai, Nan Ruan, Ye Wang, Na Xu, Zhiwen Yu, Xiaoche Wang, Hao Chen, Jiahao Lu, Hai Xu, Zhengjin Xu, Wenfu Chen, Quan Xu","doi":"10.1111/nph.20001","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n \n </p><ul>\n \n \n <li>The shape of rice grains not only determines the thousand-grain weight but also correlates closely with the grain quality.</li>\n \n \n <li>Here we identified an ultra-large grain accession (ULG) with a thousand-grain weight exceeding 60 g. The integrated analysis of QTL, BSA, <i>de novo</i> genome assembled, transcription sequencing, and gene editing was conducted to dissect the molecular basis of the ULG formation.</li>\n \n \n <li>The ULG pyramided advantageous alleles from at least four known grain-shaping genes, <i>OsLG3</i>, <i>OsMADS1</i>, <i>GS3</i>, <i>GL3.1</i>, and one novel locus, <i>qULG2-b</i>, which encoded a leucine-rich repeat receptor-like kinase. The collective impacts of <i>OsLG3</i>, <i>OsMADS1</i>, <i>GS3</i>, and <i>GL3.1</i> on grain size were confirmed in transgenic plants and near-isogenic lines. The transcriptome analysis identified 112 genes cooperatively regulated by these four genes that were prominently involved in photosynthesis and carbon metabolism. By leveraging the pleiotropy of these genes, we enhanced the grain yield, appearance, and stress tolerance of rice var. SN265.</li>\n \n \n <li>Beyond showcasing the pyramiding of multiple grain size regulation genes that can produce ULG, our study provides a theoretical framework and valuable genomic resources for improving rice variety by leveraging the pleiotropy of grain size regulated genes.</li>\n </ul>\n \n </div>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":null,"pages":null},"PeriodicalIF":8.3000,"publicationDate":"2024-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/nph.20001","RegionNum":1,"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 shape of rice grains not only determines the thousand-grain weight but also correlates closely with the grain quality.
Here we identified an ultra-large grain accession (ULG) with a thousand-grain weight exceeding 60 g. The integrated analysis of QTL, BSA, de novo genome assembled, transcription sequencing, and gene editing was conducted to dissect the molecular basis of the ULG formation.
The ULG pyramided advantageous alleles from at least four known grain-shaping genes, OsLG3, OsMADS1, GS3, GL3.1, and one novel locus, qULG2-b, which encoded a leucine-rich repeat receptor-like kinase. The collective impacts of OsLG3, OsMADS1, GS3, and GL3.1 on grain size were confirmed in transgenic plants and near-isogenic lines. The transcriptome analysis identified 112 genes cooperatively regulated by these four genes that were prominently involved in photosynthesis and carbon metabolism. By leveraging the pleiotropy of these genes, we enhanced the grain yield, appearance, and stress tolerance of rice var. SN265.
Beyond showcasing the pyramiding of multiple grain size regulation genes that can produce ULG, our study provides a theoretical framework and valuable genomic resources for improving rice variety by leveraging the pleiotropy of grain size regulated genes.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.