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The Binding Sites for the Chromatin Insulator Protein CTCF Map to DNA Methylation-Free Domains Genome-Wide
Author(s) -
Rituparna Mukhopadhyay,
Wenqiang Yu,
Joanne Whitehead,
JunWang Xu,
Magda Lezcano,
Svetlana Pack,
Chandrasekhar Kanduri,
Meena Kanduri,
Vasudeva Ginjala,
Alexander A. Vostrov,
Wolfgang Quitschke,
Igor Chernukhin,
Elena Klenova,
Victor V. Lobanenkov,
Rolf Ohlsson
Publication year - 2004
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.2408304
Subject(s) - ctcf , biology , chromatin , dna methylation , epigenetics , heterochromatin , genetics , insulator (electricity) , enhancer , computational biology , dna , gene , gene expression , electrical engineering , engineering
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.

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