Deplus, Rachel, Rajavelu, Arumugam, Boukaba, Abdelhalim, Defrance, Matthieu, Luciani, Judith, Rothé, Françoise, Dedeurwaerder, Sarah, Denis, Hélène, Brinkman, Arie B., Simmer, Femke, Müller, Fabian, Bertin, Benjamin, Berdasco, Maria, Putmans, Pascale, Calonne, Emilie, Litchfield, David W., Launoit, Yvande, Jurkowski, Tomasz P. ORCID: https://orcid.org/0000-0002-2012-0240, Stunnenberg, Hendrik G., Bock, Christoph, Sotiriou, Christos, Fraga, Mario F., Esteller, Manel, Jeltsch, Albert and Fuks, François 2014. Regulation of DNA methylation patterns by CK2-mediated phosphorylation of Dnmt3a. Cell Reports 8 (3) , 743—753. 10.1016/j.celrep.2014.06.048 |
Abstract
DNA methylation is a central epigenetic modification that is established by de novo DNA methyltransferases. The mechanisms underlying the generation of genomic methylation patterns are still poorly understood. Using mass spectrometry and a phosphospecific Dnmt3a antibody, we demonstrate that CK2 phosphorylates endogenous Dnmt3a at two key residues located near its PWWP domain, thereby downregulating the ability of Dnmt3a to methylate DNA. Genome-wide DNA methylation analysis shows that CK2 primarily modulates CpG methylation of several repeats, most notably of Alu SINEs. This modulation can be directly attributed to CK2-mediated phosphorylation of Dnmt3a. We also find that CK2-mediated phosphorylation is required for localization of Dnmt3a to heterochromatin. By revealing phosphorylation as a mode of regulation of de novo DNA methyltransferase function and by uncovering a mechanism for the regulation of methylation at repetitive elements, our results shed light on the origin of DNA methylation patterns.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Biosciences |
Publisher: | Elsevier |
ISSN: | 2211-1247 |
Date of Acceptance: | 23 June 2014 |
Last Modified: | 25 Oct 2022 13:08 |
URI: | https://orca.cardiff.ac.uk/id/eprint/118961 |
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