栽培水稻的起源、演化及超级杂交稻产量性状杂种优势的基因组特征。

IF 4.4 1区 生物学 Q1 BIOLOGY
Yiyong Zhao, Tao Li, Daliang Liu, Hao Yin, Liang Wang, Song Lu, Houlin Yu, Xinhao Sun, Taikui Zhang, Quanzhi Zhao
{"title":"栽培水稻的起源、演化及超级杂交稻产量性状杂种优势的基因组特征。","authors":"Yiyong Zhao, Tao Li, Daliang Liu, Hao Yin, Liang Wang, Song Lu, Houlin Yu, Xinhao Sun, Taikui Zhang, Quanzhi Zhao","doi":"10.1186/s12915-025-02255-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Understanding the evolutionary history of cultivated rice (Oryza sativa) and the genomic basis of heterosis is crucial for advancing rice productivity and ensuring global food security. The origins of the two main subspecies, indica and japonica, remain contentious, with debates over single versus multiple domestication events. Additionally, the genetic mechanisms underlying heterosis in elite super-hybrid rice varieties are not fully elucidated.</p><p><strong>Results: </strong>We performed a comprehensive genome-scale phylogenomic analysis using 33 high-quality Oryzeae genomes, integrating 39,984 gene trees. Our findings support the independent origins of indica and japonica subspecies, with molecular dating and synonymous substitution rates indicating nearly synchronous evolutionary trajectories. Analysis of 1383 gene duplications in the common ancestor of O. sativa revealed their involvement in vital biological processes and environmental adaptability. Phylogenomic analyses revealed no significant genomic signatures indicative of extensive hybridization events between the progenitors of indica and japonica. Newly generated 71.67 Gb of whole-genome sequencing data of five elite super-hybrid rice varieties and their progenitors uncovered differential positive selection and genetic exchanges between subspecies, contributing to heterosis formation. Transcriptome analyses highlighted the predominance of non-additive gene expression in heterosis, especially in genes related to DNA repair and recombination. Furthermore, expression quantitative trait locus (eQTL) and de novo mutation analyses identified key developmental and stress response genes, offering potential targets for enhancing heterosis.</p><p><strong>Conclusions: </strong>Our study provides robust evidence for the independent domestication of indica and japonica rice subspecies and elucidates the genomic features associated with heterosis in super-hybrid rice. By identifying key genes linked to adaptability and heterosis, we offer valuable insights and genetic resources for breeding programs aimed at improving rice yield and resilience. These findings enhance our understanding of rice evolution and the complex genetic factors driving heterosis, contributing to future strategies for agricultural productivity enhancement.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":"23 1","pages":"153"},"PeriodicalIF":4.4000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12139199/pdf/","citationCount":"0","resultStr":"{\"title\":\"The origin and evolution of cultivated rice and genomic signatures of heterosis for yield traits in super-hybrid rice.\",\"authors\":\"Yiyong Zhao, Tao Li, Daliang Liu, Hao Yin, Liang Wang, Song Lu, Houlin Yu, Xinhao Sun, Taikui Zhang, Quanzhi Zhao\",\"doi\":\"10.1186/s12915-025-02255-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Understanding the evolutionary history of cultivated rice (Oryza sativa) and the genomic basis of heterosis is crucial for advancing rice productivity and ensuring global food security. The origins of the two main subspecies, indica and japonica, remain contentious, with debates over single versus multiple domestication events. Additionally, the genetic mechanisms underlying heterosis in elite super-hybrid rice varieties are not fully elucidated.</p><p><strong>Results: </strong>We performed a comprehensive genome-scale phylogenomic analysis using 33 high-quality Oryzeae genomes, integrating 39,984 gene trees. Our findings support the independent origins of indica and japonica subspecies, with molecular dating and synonymous substitution rates indicating nearly synchronous evolutionary trajectories. Analysis of 1383 gene duplications in the common ancestor of O. sativa revealed their involvement in vital biological processes and environmental adaptability. Phylogenomic analyses revealed no significant genomic signatures indicative of extensive hybridization events between the progenitors of indica and japonica. Newly generated 71.67 Gb of whole-genome sequencing data of five elite super-hybrid rice varieties and their progenitors uncovered differential positive selection and genetic exchanges between subspecies, contributing to heterosis formation. Transcriptome analyses highlighted the predominance of non-additive gene expression in heterosis, especially in genes related to DNA repair and recombination. Furthermore, expression quantitative trait locus (eQTL) and de novo mutation analyses identified key developmental and stress response genes, offering potential targets for enhancing heterosis.</p><p><strong>Conclusions: </strong>Our study provides robust evidence for the independent domestication of indica and japonica rice subspecies and elucidates the genomic features associated with heterosis in super-hybrid rice. By identifying key genes linked to adaptability and heterosis, we offer valuable insights and genetic resources for breeding programs aimed at improving rice yield and resilience. These findings enhance our understanding of rice evolution and the complex genetic factors driving heterosis, contributing to future strategies for agricultural productivity enhancement.</p>\",\"PeriodicalId\":9339,\"journal\":{\"name\":\"BMC Biology\",\"volume\":\"23 1\",\"pages\":\"153\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-06-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12139199/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s12915-025-02255-2\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-025-02255-2","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:了解栽培水稻(Oryza sativa)的进化历史和杂种优势的基因组基础对于提高水稻生产力和确保全球粮食安全至关重要。籼稻和粳稻这两个主要亚种的起源仍然存在争议,争论的焦点是单一驯化还是多重驯化。此外,超级杂交稻优良品种杂种优势的遗传机制尚未完全阐明。结果:我们对33个高质量的稻谷基因组进行了全面的基因组级系统基因组分析,整合了39,984个基因树。我们的研究结果支持籼稻和粳稻亚种的独立起源,分子定年和同义替代率表明几乎同步的进化轨迹。对sativa共同祖先的1383个重复基因的分析揭示了它们参与重要的生物过程和环境适应性。系统基因组学分析显示,籼稻和粳稻祖先之间没有显著的基因组特征表明广泛的杂交事件。新生成的5个超级杂交稻优良品种及其祖先的71.67 Gb全基因组测序数据揭示了亚种之间的差异正选择和遗传交换,有助于杂种优势的形成。转录组分析强调了非加性基因表达在杂种优势中的优势,特别是与DNA修复和重组相关的基因。此外,通过表达数量性状位点(quantitative trait locus, eQTL)和新生突变(de novo mutation)分析,确定了关键的发育和应激反应基因,为增强杂种优势提供了潜在的靶点。结论:本研究为籼稻和粳稻亚种的独立驯化提供了有力证据,阐明了超级杂交稻杂种优势的基因组特征。通过鉴定与适应性和杂种优势相关的关键基因,我们为旨在提高水稻产量和抗逆性的育种计划提供了宝贵的见解和遗传资源。这些发现增强了我们对水稻进化和驱动杂种优势的复杂遗传因素的理解,有助于未来提高农业生产力的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The origin and evolution of cultivated rice and genomic signatures of heterosis for yield traits in super-hybrid rice.

Background: Understanding the evolutionary history of cultivated rice (Oryza sativa) and the genomic basis of heterosis is crucial for advancing rice productivity and ensuring global food security. The origins of the two main subspecies, indica and japonica, remain contentious, with debates over single versus multiple domestication events. Additionally, the genetic mechanisms underlying heterosis in elite super-hybrid rice varieties are not fully elucidated.

Results: We performed a comprehensive genome-scale phylogenomic analysis using 33 high-quality Oryzeae genomes, integrating 39,984 gene trees. Our findings support the independent origins of indica and japonica subspecies, with molecular dating and synonymous substitution rates indicating nearly synchronous evolutionary trajectories. Analysis of 1383 gene duplications in the common ancestor of O. sativa revealed their involvement in vital biological processes and environmental adaptability. Phylogenomic analyses revealed no significant genomic signatures indicative of extensive hybridization events between the progenitors of indica and japonica. Newly generated 71.67 Gb of whole-genome sequencing data of five elite super-hybrid rice varieties and their progenitors uncovered differential positive selection and genetic exchanges between subspecies, contributing to heterosis formation. Transcriptome analyses highlighted the predominance of non-additive gene expression in heterosis, especially in genes related to DNA repair and recombination. Furthermore, expression quantitative trait locus (eQTL) and de novo mutation analyses identified key developmental and stress response genes, offering potential targets for enhancing heterosis.

Conclusions: Our study provides robust evidence for the independent domestication of indica and japonica rice subspecies and elucidates the genomic features associated with heterosis in super-hybrid rice. By identifying key genes linked to adaptability and heterosis, we offer valuable insights and genetic resources for breeding programs aimed at improving rice yield and resilience. These findings enhance our understanding of rice evolution and the complex genetic factors driving heterosis, contributing to future strategies for agricultural productivity enhancement.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信