{"title":"Regulatory and evolutionary impact of DNA methylation in two songbird species and their naturally occurring F<sub>1</sub> hybrids.","authors":"Jesper Boman, Anna Qvarnström, Carina F Mugal","doi":"10.1186/s12915-024-01920-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Regulation of transcription by DNA methylation in 5'-CpG-3' context is a widespread mechanism allowing differential expression of genetically identical cells to persist throughout development. Consequently, differences in DNA methylation can reinforce variation in gene expression among cells, tissues, populations, and species. Despite a surge in studies on DNA methylation, we know little about the importance of DNA methylation in population differentiation and speciation. Here we investigate the regulatory and evolutionary impact of DNA methylation in five tissues of two Ficedula flycatcher species and their naturally occurring F<sub>1</sub> hybrids.</p><p><strong>Results: </strong>We show that the density of CpG in the promoters of genes determines the strength of the association between DNA methylation and gene expression. The impact of DNA methylation on gene expression varies among tissues with the brain showing unique patterns. Differentially expressed genes between parental species are predicted by genetic and methylation differentiation in CpG-rich promoters. However, both these factors fail to predict hybrid misexpression suggesting that promoter mismethylation is not a main determinant of hybrid misexpression in Ficedula flycatchers. Using allele-specific methylation estimates in hybrids, we also determine the genome-wide contribution of cis- and trans effects in DNA methylation differentiation. These distinct mechanisms are roughly balanced in all tissues except the brain, where trans differences predominate.</p><p><strong>Conclusions: </strong>Overall, this study provides insight on the regulatory and evolutionary impact of DNA methylation in songbirds.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11134931/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-024-01920-2","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
Abstract
Background: Regulation of transcription by DNA methylation in 5'-CpG-3' context is a widespread mechanism allowing differential expression of genetically identical cells to persist throughout development. Consequently, differences in DNA methylation can reinforce variation in gene expression among cells, tissues, populations, and species. Despite a surge in studies on DNA methylation, we know little about the importance of DNA methylation in population differentiation and speciation. Here we investigate the regulatory and evolutionary impact of DNA methylation in five tissues of two Ficedula flycatcher species and their naturally occurring F1 hybrids.
Results: We show that the density of CpG in the promoters of genes determines the strength of the association between DNA methylation and gene expression. The impact of DNA methylation on gene expression varies among tissues with the brain showing unique patterns. Differentially expressed genes between parental species are predicted by genetic and methylation differentiation in CpG-rich promoters. However, both these factors fail to predict hybrid misexpression suggesting that promoter mismethylation is not a main determinant of hybrid misexpression in Ficedula flycatchers. Using allele-specific methylation estimates in hybrids, we also determine the genome-wide contribution of cis- and trans effects in DNA methylation differentiation. These distinct mechanisms are roughly balanced in all tissues except the brain, where trans differences predominate.
Conclusions: Overall, this study provides insight on the regulatory and evolutionary impact of DNA methylation in songbirds.
背景:DNA 甲基化在 5'-CpG-3' 上下文中对转录的调控是一种广泛的机制,可使基因相同的细胞在整个发育过程中保持不同的表达。因此,DNA 甲基化的差异会加强细胞、组织、种群和物种之间基因表达的差异。尽管对 DNA 甲基化的研究激增,但我们对 DNA 甲基化在种群分化和物种分化中的重要性知之甚少。在这里,我们研究了DNA甲基化在两种飞鸟及其自然发生的F1杂交种的五个组织中的调控和进化影响:结果:我们发现基因启动子中 CpG 的密度决定了 DNA 甲基化与基因表达之间的关联强度。DNA 甲基化对基因表达的影响因组织而异,大脑显示出独特的模式。富含 CpG 的启动子中的基因和甲基化分化可预测亲本物种之间表达不同的基因。然而,这两个因素都无法预测杂交后的错误表达,这表明启动子错甲基化并不是捕蝇草杂交后错误表达的主要决定因素。利用杂交种中等位基因特异性甲基化估计值,我们还确定了 DNA 甲基化分化中顺式效应和反式效应的全基因组贡献。这些不同的机制在除大脑以外的所有组织中大致平衡,在大脑中反式差异占主导地位:总之,这项研究为鸣禽 DNA 甲基化的调控和进化影响提供了见解。
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.