期刊
EMBO JOURNAL
卷 20, 期 22, 页码 6394-6403出版社
OXFORD UNIV PRESS
DOI: 10.1093/emboj/20.22.6394
关键词
B cells; gene expression; hyperacetylation; immunoglobulin heavy chain
资金
- NIGMS NIH HHS [GM38925, R01 GM038925] Funding Source: Medline
The immunoglobulin heavy chain (IgH) gene locus spans several megabases. We show that IgH activation during B-cell differentiation, as measured by histone acetylation, occurs in discrete, independently regulated domains. Initially, a 120 kb domain of germline DNA is hyperacetylated, that extends from D-FL16.1, the 5'-most D-H gene segment, to the intergenic region between C mu and C delta. Germline V-H genes were not hyperacetylated at this stage, which accounts for D-H to J(H) recombination occurring first during B-cell development. Subsequent activation of the V-H locus happens in at least three differentially regulated domains: an interleukin-7-regulated domain consisting of the 5' J558 family, an intermediate domain and the 3' V-H genes, which are hyperacetylated in response to DJ(H) recombination. These observations lead to mechanisms for two well-documented phenomena in B-cell ontogeny: the sequential rearrangement of D-H followed by V-H gene segments, and the preferential recombination of D-H-proximal V-H genes in pro-B cells. We suggest that stepwise activation may be a general mechanism by which large segments of the genome are prepared for expression.
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