| Literature DB >> 18849521 |
Diego Ottaviani1, Elliott Lever, Richard Mitter, Tania Jones, Tim Forshew, Rossitza Christova, Eleni M Tomazou, Vardhman K Rakyan, Stephen A Krawetz, Adrian E Platts, Badmavady Segarane, Stephan Beck, Denise Sheer.
Abstract
The folding of chromatin into topologically constrained loop domains is essential for genomic function. We have identified genomic anchors that define the organization of chromatin loop domains across the human major histocompatibility complex (MHC). This locus contains critical genes for immunity and is associated with more diseases than any other region of the genome. Classical MHC genes are expressed in a cell type-specific pattern and can be induced by cytokines such as interferon-gamma (IFNG). Transcriptional activation of the MHC was associated with a reconfiguration of chromatin architecture resulting from the formation of additional genomic anchors. These findings suggest that the dynamic arrangement of genomic anchors and loops plays a role in transcriptional regulation.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18849521 PMCID: PMC2577859 DOI: 10.1101/gr.082313.108
Source DB: PubMed Journal: Genome Res ISSN: 1088-9051 Impact factor: 9.043