Please use this identifier to cite or link to this item: http://dx.doi.org/10.18419/opus-10057
Authors: Rajavelu, Arumugam
Lungu, Cristiana
Emperle, Max
Dukatz, Michael
Bröhm, Alexander
Broche, Julian
Hanelt, Ines
Parsa, Edris
Schiffers, Sarah
Karnik, Rahul
Meissner, Alexander
Carell, Thomas
Rathert, Philipp
Jurkowska, Renata Z.
Jeltsch, Albert
Title: Chromatin-dependent allosteric regulation of DNMT3A activity by MeCP2
Issue Date: 2018
metadata.ubs.publikation.typ: Zeitschriftenartikel
metadata.ubs.publikation.seiten: 9044-9056
metadata.ubs.publikation.source: Nucleic acids research 46 (2018), Seite 9044-9056
URI: http://elib.uni-stuttgart.de/handle/11682/10074
http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-100746
http://dx.doi.org/10.18419/opus-10057
ISSN: 1362-4962
0305-1048
Abstract: Despite their central importance in mammalian development, the mechanisms that regulate the DNA methylation machinery and thereby the generation of genomic methylation patterns are still poorly understood. Here, we identify the 5mC-binding protein MeCP2 as a direct and strong interactor of DNA methyltransferase 3 (DNMT3) proteins. We mapped the interaction interface to the transcriptional repression domain of MeCP2 and the ADD domain of DNMT3A and find that binding of MeCP2 strongly inhibits the activity of DNMT3A in vitro. This effect was reinforced by cellular studies where a global reduction of DNA methylation levels was observed after overexpression of MeCP2 in human cells. By engineering conformationally locked DNMT3A variants as novel tools to study the allosteric regulation of this enzyme, we show that MeCP2 stabilizes the closed, autoinhibitory conformation of DNMT3A. Interestingly, the interaction with MeCP2 and its resulting inhibition were relieved by the binding of K4 unmodified histone H3 N-terminal tail to the DNMT3A-ADD domain. Taken together, our data indicate that the localization and activity of DNMT3A are under the combined control of MeCP2 and H3 tail modifications where, depending on the modification status of the H3 tail at the binding sites, MeCP2 can act as either a repressor or activator of DNA methylation.
Appears in Collections:03 Fakultät Chemie

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