| Literature DB >> 29262320 |
Nicolas Veland1, Swanand Hardikar2, Yi Zhong2, Sitaram Gayatri1, Jiameng Dan2, Brian D Strahl3, Scott B Rothbart4, Mark T Bedford1, Taiping Chen5.
Abstract
DNA methylation plays crucial roles in chromatin structure and gene expression. Aberrant DNA methylation patterns, including global hypomethylation and regional hypermethylation, are associated with cancer and implicated in oncogenic events. How DNA methylation is regulated in developmental and cellular processes and dysregulated in cancer is poorly understood. Here, we show that PRMT6, a protein arginine methyltransferase responsible for asymmetric dimethylation of histone H3 arginine 2 (H3R2me2a), negatively regulates DNA methylation and that PRMT6 upregulation contributes to global DNA hypomethylation in cancer. Mechanistically, PRMT6 overexpression impairs chromatin association of UHRF1, an accessory factor of DNMT1, resulting in passive DNA demethylation. The effect is likely due to elevated H3R2me2a, which inhibits the interaction between UHRF1 and histone H3. Our work identifies a mechanistic link between protein arginine methylation and DNA methylation, which is disrupted in cancer.Entities:
Keywords: DNA methylation; DNMT1; PRMT6; UHRF1; arginine methylation; cancer
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Year: 2017 PMID: 29262320 PMCID: PMC5753604 DOI: 10.1016/j.celrep.2017.11.082
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423