Center for Evolutionary Hologenomics, Globe Institute, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Lerøy Seafood Group ASA, Bergen, Norway.
Epigenetics. 2024 Dec;19(1):2392049. doi: 10.1080/15592294.2024.2392049. Epub 2024 Aug 16.
The canonical view of DNA methylation, a pivotal epigenetic regulation mechanism in eukaryotes, dictates its role as a suppressor of gene activity, particularly within promoter regions. However, this view is being challenged as it is becoming increasingly evident that the connection between DNA methylation and gene expression varies depending on the genomic location and is therefore more complex than initially thought. We examined DNA methylation levels in the gut epithelium of Atlantic salmon () using whole-genome bisulfite sequencing, which we correlated with gene expression data from RNA sequencing of the same gut tissue sample (RNA-seq). Assuming epigenetic signals might be pronounced between distinctive phenotypes, we compared large and small fish, finding 22 significant associations between 22 differentially methylated regions and 21 genes. We did not detect significant methylation differences between large and small fish. However, we observed a consistent signal of methylation levels around the transcription start sites (TSS), being negatively correlated with the expression levels of those genes. We found both negative and positive associations of methylation levels with gene expression further upstream or downstream of the TSS, revealing a more unpredictable pattern. The 21 genes showing significant methylation-expression correlations were involved in biological processes related to salmon health, such as growth and immune responses. Deciphering how DNA methylation affects the expression of such genes holds great potential for future applications. For instance, our results suggest the importance of genomic context in targeting epigenetic modifications to improve the welfare of aquaculture species like Atlantic salmon.
真核生物中至关重要的表观遗传调控机制——DNA 甲基化的典型观点认为,其作用是抑制基因活性,尤其是在启动子区域。然而,随着越来越明显的是,DNA 甲基化与基因表达之间的联系因基因组位置而异,因此比最初想象的更为复杂,这种观点正受到挑战。我们使用全基因组亚硫酸氢盐测序技术检测了大西洋鲑鱼肠道上皮细胞中的 DNA 甲基化水平,并将其与同一肠道组织样本的 RNA 测序(RNA-seq)中的基因表达数据相关联。假设表观遗传信号可能在不同的表型之间更为明显,我们比较了大鱼和小鱼,在 22 个差异甲基化区域和 21 个基因之间发现了 22 个显著关联。我们没有检测到大鱼和小鱼之间存在显著的甲基化差异。然而,我们在转录起始位点(TSS)周围观察到了一致的甲基化水平信号,与这些基因的表达水平呈负相关。我们在 TSS 上下游观察到了甲基化水平与基因表达的负相关和正相关,揭示了一种更不可预测的模式。表现出显著甲基化-表达相关性的 21 个基因参与了与鲑鱼健康相关的生物学过程,如生长和免疫反应。阐明 DNA 甲基化如何影响这些基因的表达具有很大的应用潜力。例如,我们的结果表明基因组背景在靶向表观遗传修饰以提高大西洋鲑等水产养殖物种福利方面的重要性。