CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2
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- 11 July 2006
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 103 (28), 10684-10689
- https://doi.org/10.1073/pnas.0600326103
Abstract
It is thought that the H19 imprinting control region (ICR) directs the silencing of the maternally inherited Igf2 allele through a CTCF-dependent chromatin insulator. The ICR has been shown to interact physically with a silencer region in Igf2, differentially methylated region (DMR)1, but the role of CTCF in this chromatin loop and whether it restricts the physical access of distal enhancers to Igf2 is not known. We performed systematic chromosome conformation capture analyses in the Igf2/H19 region over >160 kb, identifying sequences that interact physically with the distal enhancers and the ICR. We found that, on the paternal chromosome, enhancers interact with the Igf2 promoters but that, on the maternal allele, this is prevented by CTCF binding within the H19 ICR. CTCF binding in the maternal ICR regulates its interaction with matrix attachment region (MAR)3 and DMR1 at Igf2, thus forming a tight loop around the maternal Igf2 locus, which may contribute to its silencing. Mutation of CTCF binding sites in the H19 ICR leads to loss of CTCF binding and de novo methylation of a CTCF target site within Igf2 DMR1, showing that CTCF can coordinate regional epigenetic marks. This systematic chromosome conformation capture analysis of an imprinting cluster reveals that CTCF has a critical role in the epigenetic regulation of higher-order chromatin structure and gene silencing over considerable distances in the genome.Keywords
This publication has 45 references indexed in Scilit:
- Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndromeNature Genetics, 2004
- Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loopsNature Genetics, 2004
- The Binding Sites for the Chromatin Insulator Protein CTCF Map to DNA Methylation-Free Domains Genome-WideGenome Research, 2004
- An enhancer element at the Igf2/H19 locus drives gene expression in both imprinted and non-imprinted tissuesDevelopmental Biology, 2004
- CTCF Elements Direct Allele-Specific Undermethylation at the Imprinted H19 LocusCurrent Biology, 2004
- Mutation of a Single CTCF Target Site within the H19 Imprinting Control Region Leads to Loss of Igf2 Imprinting and Complex Patterns of De Novo Methylation upon Maternal InheritanceMolecular and Cellular Biology, 2004
- Transgenic RNAi Reveals Essential Function for CTCF in H19 Gene ImprintingScience, 2004
- CTCF Tethers an Insulator to Subnuclear Sites, Suggesting Shared Insulator Mechanisms across SpeciesMolecular Cell, 2004
- Did genomic imprinting and X chromosome inactivation arise from stochastic expression?Trends in Genetics, 2001
- Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19Nature Genetics, 2000