Abstract
BackgroundDNA 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.ResultsBy 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.ConclusionWe report hundreds of genes that affect DNA methylation and provide key insights in the principles underlying epigenetic regulation.
Highlights
DNA methylation is a key epigenetic modification in human development and disease, yet there is limited understanding of its highly coordinated regulation
We identified predictive genetic variants for the expression of each gene in our data and aggregated these into single predictive scores termed genetic instruments (GIs) [13]. We used these GIs as causal anchors to establish directed effects of gene expression on genome-wide DNA methylation levels, while ensuring that these associations were specific by accounting for linkage disequilibrium (LD) and pleiotropy among neighboring GIs
We focused the analysis on 11,830 expressed genes
Summary
DNA methylation is a key epigenetic modification in human development and disease, yet there is limited understanding of its highly coordinated regulation. DNA methylation is a key component of the epigenome that controls, stabilizes, and/ or marks the transcriptional potential of a genomic region [5]. It involves the addition of a methyl group onto cytosines, mainly at CpG dinucleotides. Considerable research has been devoted to studying the enzymes that write, maintain, and erase DNA methylation (i.e., DNMTs and TETs) [6], less is known about factors that are otherwise involved in the regulation of DNA methylation. A comprehensive genome-wide survey of genes affecting DNA methylation in humans is currently lacking
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