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ABSTRACT: Background
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.Results
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.Conclusion
We report hundreds of genes that affect DNA methylation and provide key insights in the principles underlying epigenetic regulation.
SUBMITTER: Hop PJ
PROVIDER: S-EPMC7453518 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature
Hop Paul J PJ Luijk René R Daxinger Lucia L van Iterson Maarten M Dekkers Koen F KF Jansen Rick R van Meurs Joyce B J JBJ 't Hoen Peter A C PAC Ikram M Arfan MA van Greevenbroek Marleen M J MMJ Boomsma Dorret I DI Slagboom P Eline PE Veldink Jan H JH van Zwet Erik W EW Heijmans Bastiaan T BT
Genome biology 20200828 1
<h4>Background</h4>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.<h4>Results</h4>By employing genetic instruments as causal anchors, we establish directed associations between gene expression and distant DNA methylation levels, while ensuring specificity of the association ...[more]