A bipartite element with allele-specific functions safeguards DNA methylation imprints at the Dlk1-Dio3 locus Journal Article


Authors: Aronson, B. E.; Scourzic, L.; Shah, V.; Swanzey, E.; Kloetgen, A.; Polyzos, A.; Sinha, A.; Azziz, A.; Caspi, I.; Li, J.; Pelham-Webb, B.; Glenn, R. A.; Vierbuchen, T.; Wichterle, H.; Tsirigos, A.; Dawlaty, M. M.; Stadtfeld, M.; Apostolou, E.
Article Title: A bipartite element with allele-specific functions safeguards DNA methylation imprints at the Dlk1-Dio3 locus
Abstract: Loss of imprinting (LOI) results in severe developmental defects, but the mechanisms preventing LOI remain incompletely understood. Here, we dissect the functional components of the imprinting control region of the essential Dlk1-Dio3 locus (called IG-DMR) in pluripotent stem cells. We demonstrate that the IG-DMR consists of two antagonistic elements: a paternally methylated CpG island that prevents recruitment of TET dioxygenases and a maternally unmethylated non-canonical enhancer that ensures expression of the Gtl2 lncRNA by counteracting de novo DNA methyltransferases. Genetic or epigenetic editing of these elements leads to distinct LOI phenotypes with characteristic alternations of allele-specific gene expression, DNA methylation, and 3D chromatin topology. Although repression of the Gtl2 promoter results in dysregulated imprinting, the stability of LOI phenotypes depends on the IG-DMR, suggesting a functional hierarchy. These findings establish the IG-DMR as a bipartite control element that maintains imprinting by allele-specific restriction of the DNA (de)methylation machinery. © 2021 Elsevier Inc.
Keywords: dna methylation; pluripotent stem cells; genomic imprinting; enhancer; bipartite element; dlk1-dio3; dnmt3; epigenome editing; ig-dmr; tet enzymes
Journal Title: Developmental Cell
Volume: 56
Issue: 22
ISSN: 1534-5807
Publisher: Cell Press  
Date Published: 2021-11-22
Start Page: 3052
End Page: 3065.e5
Language: English
DOI: 10.1016/j.devcel.2021.10.004
PROVIDER: scopus
PMCID: PMC8628258
PUBMED: 34710357
DOI/URL:
Notes: Article -- Export Date: 1 December 2021 -- Source: Scopus
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  1. Inbal Caspi
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  2. Rachel Glenn
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