Jian Che, Tao Yang, Haichuan Yang, Guangwei Li, Zhengji Wang, Qinglu Zhang, Xu Li, Yidan Ouyang
{"title":"三个亚种内和亚种间杂交稻杂种优势的遗传和转录组学基础","authors":"Jian Che, Tao Yang, Haichuan Yang, Guangwei Li, Zhengji Wang, Qinglu Zhang, Xu Li, Yidan Ouyang","doi":"10.1093/plphys/kiaf427","DOIUrl":null,"url":null,"abstract":"Heterosis has been crucial for global food security, particularly in hybrid rice (Oryza sativa L.) development. While indica-japonica intersubspecific hybrids offer a 20-30% yield increase over indica-indica hybrids, the mechanisms underlying intersubspecific heterosis remain poorly explored. Here, we sequenced and phenotyped three pairwise crosses and their derived populations from representative japonica and indica varieties. Intersubspecific hybrids exhibited stronger heterosis and superior biomass than intrasubspecific hybrids. Transcriptomic analysis demonstrated that brassinosteroid signaling and flowering-promoting genes are up-regulated in intrasubspecific hybrids to accelerate growth, while intersubspecific hybrids display enhanced tillering capacity and yield potential through elevated transcriptional activity and gene expression related to nitrogen use efficiency. Genome-wide allele-specific expression analysis highlighted the regulatory impact of parental genomic divergence on hybrid gene expression, particularly through promoter variations affecting genes involved in flowering, tillering, pollen fertility, and stress response. QTL mapping revealed a greater number of loci associated with heterosis in intersubspecific hybrids than in intrasubspecific hybrids, particularly for spikelets per panicle and plant height, where the Nipponbare allele and indica alleles function as advantageous alleles across distinct QTLs; their synergistic interactions collectively drive the heterosis between subspecies. Our study reveals that parental genetic diversity combined with dominant expression patterns collectively drives heterosis, providing valuable insights for optimizing intersubspecific hybrid rice breeding to enhance yield and agricultural sustainability.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"17 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic and transcriptomic basis of heterosis in three intra- and intersubspecific hybrid rice\",\"authors\":\"Jian Che, Tao Yang, Haichuan Yang, Guangwei Li, Zhengji Wang, Qinglu Zhang, Xu Li, Yidan Ouyang\",\"doi\":\"10.1093/plphys/kiaf427\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Heterosis has been crucial for global food security, particularly in hybrid rice (Oryza sativa L.) development. While indica-japonica intersubspecific hybrids offer a 20-30% yield increase over indica-indica hybrids, the mechanisms underlying intersubspecific heterosis remain poorly explored. Here, we sequenced and phenotyped three pairwise crosses and their derived populations from representative japonica and indica varieties. Intersubspecific hybrids exhibited stronger heterosis and superior biomass than intrasubspecific hybrids. Transcriptomic analysis demonstrated that brassinosteroid signaling and flowering-promoting genes are up-regulated in intrasubspecific hybrids to accelerate growth, while intersubspecific hybrids display enhanced tillering capacity and yield potential through elevated transcriptional activity and gene expression related to nitrogen use efficiency. Genome-wide allele-specific expression analysis highlighted the regulatory impact of parental genomic divergence on hybrid gene expression, particularly through promoter variations affecting genes involved in flowering, tillering, pollen fertility, and stress response. QTL mapping revealed a greater number of loci associated with heterosis in intersubspecific hybrids than in intrasubspecific hybrids, particularly for spikelets per panicle and plant height, where the Nipponbare allele and indica alleles function as advantageous alleles across distinct QTLs; their synergistic interactions collectively drive the heterosis between subspecies. Our study reveals that parental genetic diversity combined with dominant expression patterns collectively drives heterosis, providing valuable insights for optimizing intersubspecific hybrid rice breeding to enhance yield and agricultural sustainability.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"17 1\",\"pages\":\"\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/plphys/kiaf427\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf427","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Genetic and transcriptomic basis of heterosis in three intra- and intersubspecific hybrid rice
Heterosis has been crucial for global food security, particularly in hybrid rice (Oryza sativa L.) development. While indica-japonica intersubspecific hybrids offer a 20-30% yield increase over indica-indica hybrids, the mechanisms underlying intersubspecific heterosis remain poorly explored. Here, we sequenced and phenotyped three pairwise crosses and their derived populations from representative japonica and indica varieties. Intersubspecific hybrids exhibited stronger heterosis and superior biomass than intrasubspecific hybrids. Transcriptomic analysis demonstrated that brassinosteroid signaling and flowering-promoting genes are up-regulated in intrasubspecific hybrids to accelerate growth, while intersubspecific hybrids display enhanced tillering capacity and yield potential through elevated transcriptional activity and gene expression related to nitrogen use efficiency. Genome-wide allele-specific expression analysis highlighted the regulatory impact of parental genomic divergence on hybrid gene expression, particularly through promoter variations affecting genes involved in flowering, tillering, pollen fertility, and stress response. QTL mapping revealed a greater number of loci associated with heterosis in intersubspecific hybrids than in intrasubspecific hybrids, particularly for spikelets per panicle and plant height, where the Nipponbare allele and indica alleles function as advantageous alleles across distinct QTLs; their synergistic interactions collectively drive the heterosis between subspecies. Our study reveals that parental genetic diversity combined with dominant expression patterns collectively drives heterosis, providing valuable insights for optimizing intersubspecific hybrid rice breeding to enhance yield and agricultural sustainability.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.