The binding sites for the chromatin insulator protein CTCF map to DNA methylation-free domains genome-wide

被引:111
作者
Mukhopadhyay, R
Yu, WQ
Whitehead, J
Xu, JW
Lezcano, M
Pack, S
Kanduri, C
Kanduri, M
Ginjala, V
Vostrov, A
Quitschke, W
Chernukhin, I
Klenova, E
Lobanenkov, V
Ohlsson, R
机构
[1] Uppsala Univ, Evolut Biol Ctr, Dept Genet & Dev, S-75236 Uppsala, Sweden
[2] NIAID, Mol Pathol Sect, Immunopathol Lab, NIH, Bethesda, MD 20892 USA
[3] SUNY Stony Brook, Dept Psychiat & Behav Sci, Stony Brook, NY 11794 USA
[4] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
关键词
D O I
10.1101/gr.2408304
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All known vertebrate chromatin insulators interact with the highly conserved, multivalent II-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.
引用
收藏
页码:1594 / 1602
页数:9
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