Literature DB >> 15107847

Antisense intergenic transcription in V(D)J recombination.

Daniel J Bolland1, Andrew L Wood, Colette M Johnston, Sam F Bunting, Geoff Morgan, Lyubomira Chakalova, Peter J Fraser, Anne E Corcoran.   

Abstract

Antigen receptor genes undergo variable, diversity and joining (V(D)J) recombination, which requires ordered large-scale chromatin remodeling. Here we show that antisense transcription, both genic and intergenic, occurs extensively in the V region of the immunoglobulin heavy chain locus. RNA fluorescence in situ hybridization demonstrates antisense transcription is strictly developmentally regulated and is initiated during the transition from DJ(H) to VDJ(H) recombination and terminates concomitantly with VDJ(H) recombination. Our data show antisense transcription is specific to the V region and suggest transcripts extend across several genes. We propose that antisense transcription remodels the V region to facilitate V(H)-to-DJ(H) recombination. These findings have wider implications for V(D)J recombination of other antigen receptor loci and developmental regulation of multigene loci.

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Year:  2004        PMID: 15107847     DOI: 10.1038/ni1068

Source DB:  PubMed          Journal:  Nat Immunol        ISSN: 1529-2908            Impact factor:   25.606


  91 in total

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8.  Elucidation of IgH intronic enhancer functions via germ-line deletion.

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Journal:  Genes Dev       Date:  2005-03-01       Impact factor: 11.361

10.  Chromatin-remodeling factors mediate the balance of sense-antisense transcription at the FGF2 locus.

Authors:  Lori A McEachern; Paul R Murphy
Journal:  Mol Endocrinol       Date:  2014-02-19
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