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Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region

机译:人类H19 / IGF2印迹控制区域中的第六个CTCF结合位点存在非随机的个体特异性甲基化谱

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摘要

Expression of imprinted genes is classically associated with differential methylation of specific CpG-rich DNA regions (DMRs). The H19/IGF2 locus is considered a paradigm for epigenetic regulation. In mice, as in humans, the essential H19 DMR-target of the CTCF insulator-is located between the two genes. Here, we performed a pyrosequencing-based quantitative analysis of its CpG methylation in normal human tissues. The quantitative analysis of the methylation level in the H19 DMR revealed three unexpected discrete, individual-specific methylation states. This epigenetic polymorphism was confined to the sixth CTCF binding site while a unique median-methylated profile was found at the third CTCF binding site as well as in the H19 promoter. Monoallelic expression of H19 and IGF2 was maintained independently of the methylation status at the sixth CTCF binding site and the IGF2 DMR2 displayed a median-methylated profile in all individuals and tissues analyzed. Interestingly, the methylation profile was genetically transmitted. Transgenerational inheritance of the H19 methylation profile was compatible with a simple model involving one gene with three alleles. The existence of three individual-specific epigenotypes in the H19 DMR in a non-pathological situation means it is important to reconsider the diagnostic value and functional importance of the sixth CTCF binding site.
机译:印迹基因的表达通常与富含CpG的特定DNA区域(DMR)的甲基化差异相关。 H19 / IGF2基因座被认为是表观遗传调控的范例。与人类一样,在小鼠中,CTCF绝缘子的必需H19 DMR靶标位于两个基因之间。在这里,我们对其在正常人体组织中的CpG甲基化进行了基于焦磷酸测序的定量分析。 H19 DMR中甲基化水平的定量分析显示了三个意想不到的离散,个体特异性甲基化状态。这种表观遗传多态性仅限于第六个CTCF结合位点,而在第三个CTCF结合位点和H19启动子中发现了独特的中位甲基化谱。 H19和IGF2的单等位基因表达与第六个CTCF结合位点处的甲基化状态无关,并且在所有分析的个人和组织中,IGF2 DMR2均显示中位甲基化分布。有趣的是,甲基化图谱是遗传传递的。 H19甲基化谱图的跨代遗传与涉及一个具有三个等位基因的基因的简单模型兼容。在非病理情况下,H19 DMR中存在三种个体特异性表型,这意味着重新考虑第六个CTCF结合位点的诊断价值和功能重要性非常重要。

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