| Literature DB >> 31422875 |
Yuelin Song1, Patrick R van den Berg2, Styliani Markoulaki3, Frank Soldner3, Alessandra Dall'Agnese3, Jonathan E Henninger3, Jesse Drotar3, Nicholas Rosenau3, Malkiel A Cohen3, Richard A Young4, Stefan Semrau5, Yonatan Stelzer6, Rudolf Jaenisch7.
Abstract
Variable levels of DNA methylation have been reported at tissue-specific differential methylation regions (DMRs) overlapping enhancers, including super-enhancers (SEs) associated with key cell identity genes, but the mechanisms responsible for this intriguing behavior are not well understood. We used allele-specific reporters at the endogenous Sox2 and Mir290 SEs in embryonic stem cells and found that the allelic DNA methylation state is dynamically switching, resulting in cell-to-cell heterogeneity. Dynamic DNA methylation is driven by the balance between DNA methyltransferases and transcription factor binding on one side and co-regulated with the Mediator complex recruitment and H3K27ac level changes at regulatory elements on the other side. DNA methylation at the Sox2 and the Mir290 SEs is independently regulated and has distinct consequences on the cellular differentiation state. Dynamic allele-specific DNA methylation at the two SEs was also seen at different stages in preimplantation embryos, revealing that methylation heterogeneity occurs in vivo.Entities:
Keywords: dynamic DNA methylation; embryonic stem cells; super-enhancers; transcriptional heterogeneity
Mesh:
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Year: 2019 PMID: 31422875 PMCID: PMC6731151 DOI: 10.1016/j.molcel.2019.06.045
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970