Department of Molecular and Cellular Biology, Beckman Research Institute Duarte, CA, USA.
Front Genet. 2012 Oct 15;3:214. doi: 10.3389/fgene.2012.00214. eCollection 2012.
CTCF (CCCTC-binding factor)-mediated insulation at the H19-Insulin-like growth factor 2 (Igf2) imprinted domain is a classic example for imprinted gene regulation. DNA methylation difference in the imprinting control region (ICR) is inherited from the gametes and subsequently determines parental allele-specific enhancer blocking and imprinted expression in the soma. Recent genetic studies showed that proper monoallelic enhancer blocking at the H19-Igf2 ICR is critical for development. Strict biallelic insulation at this locus causes perinatal lethality, whereas leaky biallelic insulation results in smaller size but no lethality. Apart from enhancer blocking, CTCF is also the master organizer of chromatin composition in the maternal allele along this imprinted domain, affecting not only histone tail covalent modifications but also those in the histone core. Additionally, CTCF binding in the soma protects the maternal allele from de novo DNA methylation. CTCF binding is not involved in the establishment of the gametic marks at the ICR, but it slightly delays de novo methylation in the maternally inherited ICR allele in prospermatogonia. This review focuses on the developmental and epigenetic consequences of CTCF binding at the H19-Igf2 ICR.
CTCF(CCCTC 结合因子)介导的 H19-胰岛素样生长因子 2(Igf2)印迹域中的隔离是印迹基因调控的一个经典范例。印迹控制区(ICR)中的 DNA 甲基化差异是从配子遗传而来的,随后决定了亲本等位基因特异性增强子阻断和体细胞中的印迹表达。最近的遗传研究表明,H19-Igf2 ICR 处适当的单等位基因增强子阻断对于发育至关重要。该位点严格的双等位基因隔离会导致围产期致死,而双等位基因泄漏性隔离则会导致体型较小但不会致死。除了增强子阻断,CTCF 还是沿着这个印迹域中母体等位基因染色质组成的主要组织者,不仅影响组蛋白尾部的共价修饰,还影响组蛋白核心的修饰。此外,CTCF 在体细胞中的结合保护母体等位基因免受从头 DNA 甲基化的影响。CTCF 结合不参与 ICR 处配子标记的建立,但它会略微延迟在雄性生殖细胞中母系遗传的 ICR 等位基因中的从头甲基化。这篇综述重点介绍了 CTCF 在 H19-Igf2 ICR 上的结合对发育和表观遗传的影响。