Kurukuti Sreenivasulu, Tiwari Vijay Kumar, Tavoosidana Gholamreza, Pugacheva Elena, Murrell Adele, Zhao Zhihu, Lobanenkov Victor, Reik Wolf, Ohlsson Rolf
Department of Development and Genetics, Uppsala University, Norbyvägen 18A, S-752 36 Uppsala, Sweden.
Proc Natl Acad Sci U S A. 2006 Jul 11;103(28):10684-9. doi: 10.1073/pnas.0600326103. Epub 2006 Jun 30.
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.
人们认为,H19印记控制区(ICR)通过依赖CTCF的染色质绝缘子指导母源遗传的Igf2等位基因的沉默。ICR已被证明与Igf2中的沉默子区域、差异甲基化区域(DMR)1发生物理相互作用,但CTCF在这种染色质环中的作用以及它是否限制远端增强子对Igf2的物理接触尚不清楚。我们在超过160 kb的Igf2/H19区域进行了系统的染色体构象捕获分析,确定了与远端增强子和ICR发生物理相互作用的序列。我们发现,在父源染色体上,增强子与Igf2启动子相互作用,但在母源等位基因上,H19 ICR内的CTCF结合阻止了这种相互作用。母源ICR中的CTCF结合调节其与Igf2处的基质附着区域(MAR)3和DMR1的相互作用,从而在母源Igf2基因座周围形成一个紧密的环,这可能有助于其沉默。H19 ICR中CTCF结合位点的突变导致CTCF结合丧失和Igf2 DMR1内CTCF靶位点的从头甲基化,表明CTCF可以协调区域表观遗传标记。对一个印记簇的这种系统染色体构象捕获分析表明,CTCF在基因组中相当长距离的高阶染色质结构表观遗传调控和基因沉默中起关键作用。