{"title":"杨树杂交无性系NL895的基因组组装和DNA甲基化变异","authors":"Jie He,Guang-Zheng Diao,Yang-Fan Feng,Hao-Ran Liao,Ying Guo,Li-Na Mei,Fang-Fang Fu,Tongming Yin,Fuliang Cao,Liang-Jiao Xue","doi":"10.1093/plphys/kiaf415","DOIUrl":null,"url":null,"abstract":"Epimutant populations represent important genetic resources for plant breeding and selection. However, the variation and dynamics of epigenomic modifications among epimutants are still elusive. In this study, we analyzed DNA methylation patterns at both whole-genome and allelic levels in an epimutant population of a model hybrid poplar NL895 (Populus deltoides × P. euramericana cv. 'Nanlin895'). Epimutants were generated through the application of 5-Azacytidine (5-Aza) during tissue culture. A haplotype-resolved assembly of NL895 was constructed to serve as a reference for epigenomic analysis. Compared to control plants, averaged DNA methylation levels across the entire genome were reduced in epimutants. The methylation patterns of epimutants exhibited high diversity in several aspects, including the number of differentially methylated regions (DMRs), distribution of DMRs in sequence contexts, and genomic features. The observed epigenomic diversity suggests stochastic effects resulting from 5-Aza treatment. At the gene level, non-expressed genes consistently displayed higher rates of methylation across all examined epimutants. Among allele-specific expressed genes (ASEGs), fold changes between parental alleles were more pronounced in allele pairs exhibiting greater disparities in DNA methylation rates. For allele-specific methylation regions (ASMRs), the differences in methylation levels were notably elevated in ASMRs overlapped with genomic structural variations (SVs). Our results provide valuable germplasm resources characterized by phenotypic variations for poplar breeding, and the dynamics of DNA methylation in hybrid poplar epimutants highlights potential clues for application of hybrid vigor.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"89 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genome assembly and DNA methylation variation in an epimutant population of hybrid poplar clone NL895.\",\"authors\":\"Jie He,Guang-Zheng Diao,Yang-Fan Feng,Hao-Ran Liao,Ying Guo,Li-Na Mei,Fang-Fang Fu,Tongming Yin,Fuliang Cao,Liang-Jiao Xue\",\"doi\":\"10.1093/plphys/kiaf415\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Epimutant populations represent important genetic resources for plant breeding and selection. However, the variation and dynamics of epigenomic modifications among epimutants are still elusive. In this study, we analyzed DNA methylation patterns at both whole-genome and allelic levels in an epimutant population of a model hybrid poplar NL895 (Populus deltoides × P. euramericana cv. 'Nanlin895'). Epimutants were generated through the application of 5-Azacytidine (5-Aza) during tissue culture. A haplotype-resolved assembly of NL895 was constructed to serve as a reference for epigenomic analysis. Compared to control plants, averaged DNA methylation levels across the entire genome were reduced in epimutants. The methylation patterns of epimutants exhibited high diversity in several aspects, including the number of differentially methylated regions (DMRs), distribution of DMRs in sequence contexts, and genomic features. The observed epigenomic diversity suggests stochastic effects resulting from 5-Aza treatment. At the gene level, non-expressed genes consistently displayed higher rates of methylation across all examined epimutants. Among allele-specific expressed genes (ASEGs), fold changes between parental alleles were more pronounced in allele pairs exhibiting greater disparities in DNA methylation rates. For allele-specific methylation regions (ASMRs), the differences in methylation levels were notably elevated in ASMRs overlapped with genomic structural variations (SVs). 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引用次数: 0
摘要
表观突变体群体是植物育种和选择的重要遗传资源。然而,表观基因组修饰在表观突变体之间的变化和动态仍然是难以捉摸的。在这项研究中,我们分析了典型杂交杨树NL895 (Populus deltoides × P. euramericana cv.)的全基因组和等位基因水平的DNA甲基化模式。“Nanlin895”)。在组织培养过程中,通过应用5-氮杂胞苷(5-Aza)产生附加突变体。构建了NL895单倍型分离序列,作为表观基因组分析的参考。与对照植物相比,准突变体中整个基因组的平均DNA甲基化水平降低。表观突变体的甲基化模式在几个方面表现出高度的多样性,包括差异甲基化区域(DMRs)的数量、DMRs在序列背景中的分布和基因组特征。观察到的表观基因组多样性表明5-Aza处理引起的随机效应。在基因水平上,非表达基因在所有检测的外突变体中始终显示出较高的甲基化率。在等位基因特异性表达基因(ASEGs)中,亲本等位基因之间的折叠变化在等位基因对中更为明显,显示出DNA甲基化率的较大差异。对于等位基因特异性甲基化区(ASMRs),在与基因组结构变异(SVs)重叠的ASMRs中,甲基化水平差异显著升高。本研究结果为杨树育种提供了有价值的表型变异种质资源,杂交杨树表观突变体DNA甲基化动态为杂种优势的应用提供了潜在线索。
Genome assembly and DNA methylation variation in an epimutant population of hybrid poplar clone NL895.
Epimutant populations represent important genetic resources for plant breeding and selection. However, the variation and dynamics of epigenomic modifications among epimutants are still elusive. In this study, we analyzed DNA methylation patterns at both whole-genome and allelic levels in an epimutant population of a model hybrid poplar NL895 (Populus deltoides × P. euramericana cv. 'Nanlin895'). Epimutants were generated through the application of 5-Azacytidine (5-Aza) during tissue culture. A haplotype-resolved assembly of NL895 was constructed to serve as a reference for epigenomic analysis. Compared to control plants, averaged DNA methylation levels across the entire genome were reduced in epimutants. The methylation patterns of epimutants exhibited high diversity in several aspects, including the number of differentially methylated regions (DMRs), distribution of DMRs in sequence contexts, and genomic features. The observed epigenomic diversity suggests stochastic effects resulting from 5-Aza treatment. At the gene level, non-expressed genes consistently displayed higher rates of methylation across all examined epimutants. Among allele-specific expressed genes (ASEGs), fold changes between parental alleles were more pronounced in allele pairs exhibiting greater disparities in DNA methylation rates. For allele-specific methylation regions (ASMRs), the differences in methylation levels were notably elevated in ASMRs overlapped with genomic structural variations (SVs). Our results provide valuable germplasm resources characterized by phenotypic variations for poplar breeding, and the dynamics of DNA methylation in hybrid poplar epimutants highlights potential clues for application of hybrid vigor.
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.