Literature DB >> 18849521

Reconfiguration of genomic anchors upon transcriptional activation of the human major histocompatibility complex.

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.

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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


  55 in total

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