In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions
École Polytechnique Fédérale de Lausanne · Institute of Genetics and Biophysics
Abstract
The maintenance of H3K9 and DNA methylation at imprinting control regions (ICRs) during early embryogenesis is key to the regulation of imprinted genes. Here, we reveal that ZFP57, its cofactor KAP1, and associated effectors bind selectively to the H3K9me3-bearing, DNA-methylated allele of ICRs in ES cells. KAP1 deletion induces a loss of heterochromatin marks at ICRs, whereas deleting ZFP57 or DNMTs leads to ICR DNA demethylation. Accordingly, we find that ZFP57 and KAP1 associated with DNMTs and hemimethylated DNA-binding NP95. Finally, we identify the methylated TGCCGC hexanucleotide as the motif that is recognized by ZFP57 in all ICRs and in several tens of additional loci, several of which are at least…
Citation impact
- FWCI
- 24.55
- Percentile
- 100%
- References
- 44
Authors
11- SQSimon QuennevilleCorresponding
École Polytechnique Fédérale de Lausanne
- GVGaetano Verde
Institute of Genetics and Biophysics
- ACAndrea Corsinotti
École Polytechnique Fédérale de Lausanne
- AKAdamandia Kapopoulou
École Polytechnique Fédérale de Lausanne
- JJJohan Jakobsson
École Polytechnique Fédérale de Lausanne
Topics & keywords
- Biology
- Imprinting (psychology)
- DNA methylation
- Genomic imprinting
- Chromatin
- Methylation
- Embryonic stem cell
- Genetics