Molecular Epidemiology, Department of Biomedical Data Sciences, Leiden University Medical Center, 2333 ZC, Leiden, The Netherlands.
Department of Neurology, UMC Utrecht Brain Center, University Medical Centre Utrecht, Utrecht University, 3584 CG, Utrecht, The Netherlands.
Genome Biol. 2020 Aug 28;21(1):220. doi: 10.1186/s13059-020-02114-z.
DNA methylation is a key epigenetic modification in human development and disease, yet there is limited understanding of its highly coordinated regulation. Here, we identify 818 genes that affect DNA methylation patterns in blood using large-scale population genomics data.
By employing genetic instruments as causal anchors, we establish directed associations between gene expression and distant DNA methylation levels, while ensuring specificity of the associations by correcting for linkage disequilibrium and pleiotropy among neighboring genes. The identified genes are enriched for transcription factors, of which many consistently increased or decreased DNA methylation levels at multiple CpG sites. In addition, we show that a substantial number of transcription factors affected DNA methylation at their experimentally determined binding sites. We also observe genes encoding proteins with heterogenous functions that have widespread effects on DNA methylation, e.g., NFKBIE, CDCA7(L), and NLRC5, and for several examples, we suggest plausible mechanisms underlying their effect on DNA methylation.
We report hundreds of genes that affect DNA methylation and provide key insights in the principles underlying epigenetic regulation.
DNA 甲基化是人类发育和疾病中的一种关键表观遗传修饰,但对其高度协调的调控知之甚少。在这里,我们使用大规模的人群基因组学数据,确定了 818 个影响血液中 DNA 甲基化模式的基因。
通过将遗传工具作为因果锚点,我们在基因表达和远距离 DNA 甲基化水平之间建立了有向关联,同时通过纠正邻近基因之间的连锁不平衡和多效性,确保了关联的特异性。鉴定出的基因富含转录因子,其中许多转录因子在多个 CpG 位点上一致地增加或降低 DNA 甲基化水平。此外,我们还表明,相当数量的转录因子在其实验确定的结合位点上影响 DNA 甲基化。我们还观察到编码具有异质功能的蛋白质的基因对 DNA 甲基化有广泛的影响,例如 NFKBIE、CDCA7(L)和 NLRC5,对于其中的几个例子,我们提出了它们影响 DNA 甲基化的潜在机制。
我们报告了数百个影响 DNA 甲基化的基因,并为表观遗传调控的基本原则提供了重要的见解。