Analysis of intergenic transcription and histone modification across the human immunoglobulin heavy-chain locus

Ig class switch recombination (CSR) is initiated by activation-induced cytidine deaminase (AID) mediated deamination of the switch (S) regions; the resultant mismatch is processed to yield the DNA breaks required for recombination. Whereas many of the pathways involved in the mechanism of recombinat...

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Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 105; no. 41; pp. 15872 - 15877
Main Authors: Chowdhury, Muslima, Forouhi, Omid, Dayal, Sandeep, McCloskey, Natalie, Gould, Hannah J, Felsenfeld, Gary, Fear, David J
Format: Journal Article
Language:English
Published: United States National Academy of Sciences 14-10-2008
National Acad Sciences
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Summary:Ig class switch recombination (CSR) is initiated by activation-induced cytidine deaminase (AID) mediated deamination of the switch (S) regions; the resultant mismatch is processed to yield the DNA breaks required for recombination. Whereas many of the pathways involved in the mechanism of recombination have been identified, little is known about how CSR is regulated. AID action is known to require transcription of the Ig heavy-chain genes. However, it is not understood how AID is restricted to the Ig genes. Many aspects of gene expression are known to be regulated by modification of chromatin structure. In turn, chromatin is known to be regulated by several RNA-dependent activities. We have mapped the transcriptional and chromatin landscape of the human Ig heavy-chain locus to investigate the effect these activities have on CSR. We demonstrate that the Ig heavy-chain constant genes and 3'-regulatory regions are in an active chromatin conformation in unstimulated total human B cells: the locus undergoes both genic and intergenic transcription and possesses histone modifications associated with "active" chromatin (acetylated H3 and H4 and lysine 4 trimethylated H3). However, on cytokine stimulation, these modifications spread into the S regions, demonstrating a chromatin remodeling activity associated with switching. Surprisingly, after stimulation, the S regions also accumulate lysine 9 trimethylated H3, a modification previously associated with gene silencing. These data demonstrates that the Ig locus is maintained with a complex pattern of both positive and negative histone marks and suggest that some of these marks may have dual functions.
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Author contributions: D.J.F. designed research; M.C., O.F., N.M., and D.J.F. performed research; S.D., H.J.G., G.F., and D.J.F. analyzed data; and S.D., H.J.G., G.F., and D.J.F. wrote the paper.
Contributed by Gary Felsenfeld, August 26, 2008
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0808462105