| Literature DB >> 23650635 |
Jim R Hughes1, Karen M Lower, Ian Dunham, Stephen Taylor, Marco De Gobbi, Jacqueline A Sloane-Stanley, Simon McGowan, Jiannis Ragoussis, Douglas Vernimmen, Richard J Gibbons, Douglas R Higgs.
Abstract
We have combined the circular chromosome conformation capture protocol with high-throughput, genome-wide sequence analysis to characterize the cis-acting regulatory network at a single locus. In contrast to methods which identify large interacting regions (10-1000 kb), the 4C approach provides a comprehensive, high-resolution analysis of a specific locus with the aim of defining, in detail, the cis-regulatory elements controlling a single gene or gene cluster. Using the human α-globin locus as a model, we detected all known local and long-range interactions with this gene cluster. In addition, we identified two interactions with genes located 300 kb (NME4) and 625 kb (FAM173a) from the α-globin cluster.Entities:
Keywords: chromatin conformation capture; cis-regulatory elements; α-globin locus
Mesh:
Substances:
Year: 2013 PMID: 23650635 PMCID: PMC3682726 DOI: 10.1098/rstb.2012.0361
Source DB: PubMed Journal: Philos Trans R Soc Lond B Biol Sci ISSN: 0962-8436 Impact factor: 6.237