Mukhopadhyay Rituparna, Yu WenQiang, Whitehead Joanne, Xu JunWang, Lezcano Magda, Pack Svetlana, Kanduri Chandrasekhar, Kanduri Meena, Ginjala Vasudeva, Vostrov Alexander, Quitschke Wolfgang, Chernukhin Igor, Klenova Elena, Lobanenkov Victor, Ohlsson Rolf
Department of Development & Genetics, Evolution Biology Centre, Uppsala University, Norbyvägen 18A, S-752 36 Uppsala, Sweden.
Genome Res. 2004 Aug;14(8):1594-602. doi: 10.1101/gr.2408304. Epub 2004 Jul 15.
All known vertebrate chromatin insulators interact with the highly conserved, multivalent 11-zinc finger nuclear factor CTCF to demarcate expression domains by blocking enhancer or silencer signals in a position-dependent manner. Recent observations document that the properties of CTCF include reading and propagating the epigenetic state of the differentially methylated H19 imprinting control region. To assess whether these findings may reflect a universal role for CTCF targets, we identified more than 200 new CTCF target sites by generating DNA microarrays of clones derived from chromatin-immunopurified (ChIP) DNA followed by ChIP-on-chip hybridization analysis. Target sites include not only known loci involved in multiple cellular functions, such as metabolism, neurogenesis, growth, apoptosis, and signalling, but potentially also heterochromatic sequences. Using a novel insulator trapping assay, we also show that the majority of these targets manifest insulator functions with a continuous distribution of stringency. As these targets are generally DNA methylation-free as determined by antibodies against 5-methylcytidine and a methyl-binding protein (MBD2), a CTCF-based network correlates with genome-wide epigenetic states.
所有已知的脊椎动物染色质绝缘子都与高度保守的多价11锌指核因子CTCF相互作用,通过以位置依赖的方式阻断增强子或沉默子信号来划分表达结构域。最近的观察结果表明,CTCF的特性包括读取和传播差异甲基化的H19印记控制区域的表观遗传状态。为了评估这些发现是否可能反映CTCF靶点的普遍作用,我们通过生成来自染色质免疫纯化(ChIP)DNA的克隆DNA微阵列,随后进行芯片上ChIP杂交分析,鉴定了200多个新的CTCF靶点。靶点不仅包括参与多种细胞功能(如代谢、神经发生、生长、凋亡和信号传导)的已知基因座,还可能包括异染色质序列。使用一种新型的绝缘子捕获试验,我们还表明,这些靶点中的大多数表现出绝缘子功能,其严格程度呈连续分布。由于通过抗5-甲基胞嘧啶抗体和甲基结合蛋白(MBD2)确定这些靶点通常无DNA甲基化,基于CTCF的网络与全基因组表观遗传状态相关。