{"title":"Hybrid epigenome unveils parental genetic divergence shaping salt-tolerant heterosis in Brassica napus","authors":"Junlin Chen, Minyan Zhang, Qing Zhang, Xianfei Hou, Donghai Jia, Yuanguo Gu, Heping Wan, Hu Zhao, Jing Wen, Bin Yi, Tingdong Fu, Jinxiong Shen, Lun Zhao","doi":"10.1111/nph.70532","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n </p><ul>\n \n <li>Heterosis holds great potential for improving yield, quality, and environmental adaptability in crop breeding, which suggests that hybrids can exhibit better performance in adapting to extreme environments. However, the epigenetic mechanisms of salt-tolerant heterosis in allopolyploid crop <i>Brassica napus</i> (AACC, 2<i>n</i> = 38), particularly chromatin accessibility, remain largely unexplored.</li>\n \n <li>We investigated the dynamics of chromatin accessibility and transcriptional reprogramming during a time course of salt exposure in <i>Brassica napus</i> hybridization. We observed the importance of epigenetic and transcriptional regulation in plant resilience. The chromatin accessibility and transcriptome rapidly changed within a short time frame of salt exposure.</li>\n \n <li>Hybrid possessed more accessible chromatin and more active transcriptome than that of parents driven by epigenetic aggregation and genetic complementation. Broader and more flexible genomic resources enabled hybrid preferentially unitized advantageous alleles for salt stress adaptation. Meanwhile, these salt stress-responsive genes in hybrid exerted various heterotic effects, with non-additive genetic effects, including full-dominance, partial-dominance, and overdominance effects, playing a crucial role in salt stress adaptation.</li>\n \n <li>Our results expanded the heterosis hypothesis from an epigenetic perspective and emphasized how the combined effects of genetic and epigenetic factors enable hybrid to better withstand salt stress.</li>\n </ul>\n </div>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"248 3","pages":"1475-1490"},"PeriodicalIF":8.1000,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.70532","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
Heterosis holds great potential for improving yield, quality, and environmental adaptability in crop breeding, which suggests that hybrids can exhibit better performance in adapting to extreme environments. However, the epigenetic mechanisms of salt-tolerant heterosis in allopolyploid crop Brassica napus (AACC, 2n = 38), particularly chromatin accessibility, remain largely unexplored.
We investigated the dynamics of chromatin accessibility and transcriptional reprogramming during a time course of salt exposure in Brassica napus hybridization. We observed the importance of epigenetic and transcriptional regulation in plant resilience. The chromatin accessibility and transcriptome rapidly changed within a short time frame of salt exposure.
Hybrid possessed more accessible chromatin and more active transcriptome than that of parents driven by epigenetic aggregation and genetic complementation. Broader and more flexible genomic resources enabled hybrid preferentially unitized advantageous alleles for salt stress adaptation. Meanwhile, these salt stress-responsive genes in hybrid exerted various heterotic effects, with non-additive genetic effects, including full-dominance, partial-dominance, and overdominance effects, playing a crucial role in salt stress adaptation.
Our results expanded the heterosis hypothesis from an epigenetic perspective and emphasized how the combined effects of genetic and epigenetic factors enable hybrid to better withstand salt stress.
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.