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Complete Biallelic Insulation at the H19/Igf2 Imprinting Control Region Position Results in Fetal Growth Retardation and Perinatal Lethality

机译:在H19 / Igf2印迹控制区位置的完全双等位基因绝缘导致胎儿发育迟缓和围产期致死率

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摘要

BackgroundThe H19/Igf2 imprinting control region (ICR) functions as an insulator exclusively in the unmethylated maternal allele, where enhancer-blocking by CTCF protein prevents the interaction between the Igf2 promoter and the distant enhancers. DNA methylation inhibits CTCF binding in the paternal ICR allele. Two copies of the chicken β-globin insulator (ChβGI)2 are capable of substituting for the enhancer blocking function of the ICR. Insulation, however, now also occurs upon paternal inheritance, because unlike the H19 ICR, the (ChβGI)2 does not become methylated in fetal male germ cells. The (ChβGI)2 is a composite insulator, exhibiting enhancer blocking by CTCF and chromatin barrier functions by USF1 and VEZF1. We asked the question whether these barrier proteins protected the (ChβGI)2 sequences from methylation in the male germ line.
机译:背景H19 / Igf2印迹控制区(ICR)仅在未甲基化的母体等位基因中充当绝缘子,其中CTCF蛋白阻断增强子阻止了Igf2启动子与远距离增强子之间的相互作用。 DNA甲基化抑制了父亲ICR等位基因中的CTCF结合。鸡β-珠蛋白绝缘子(ChβGI)2的两个副本能够代替ICR的增强子阻断功能。但是,现在也可以在父系继承时进行绝缘,因为与H19 ICR不同,(ChβGI)2在胎儿雄性生殖细胞中不会甲基化。 (ChβGI)2是一种复合绝缘体,通过CTCF表现出增强剂阻断作用,并通过USF1和VEZF1表现出染色质屏障功能。我们问了一个问题,这些屏障蛋白是否能保护(ChβGI)2序列免受雄性种系中甲基化的影响。

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