Chromatin remodeling at the Ig loci prior to V(D)J recombination

被引:81
作者
Maës, J
O'Neill, LP
Cavelier, P
Turner, BM
Rougeon, F
Goodhardt, M
机构
[1] Inst Pasteur, CNRS 1960, Unite Genet & Biochim Dev, Unite Rech Associee,Dept Immunol, F-75724 Paris, France
[2] Univ Birmingham, Sch Med, Dept Anat, Birmingham, W Midlands, England
关键词
D O I
10.4049/jimmunol.167.2.866
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Rearrangement of Ig H and L chain genes is highly regulated and takes place sequentially during B cell development. Several lines of evidence indicate that chromatin may modulate accessibility of the Ig loci for V(D)J recombination. In this study, we show that remodeling of V and J segment chromatin occurs before V(D)J recombination at the endogenous H and kappa L chain loci. In recombination-activating gene-deficient pro-B cells, there is a reorganization of nucleosomal structure over the H chain J(H) Cluster and increased DNase I sensitivity of V-H and J(H) segments. The pro-B/pre-B cell transition is marked by a decrease in the DNase I sensitivity of V-H segments and a reciprocal increase in the nuclease sensitivity Of VK and J kappa segments. In contrast, J(H) segments remain DNase I sensitive, and their nucleosomal organization is maintained in mu (+) recombination-activating gene-deficient pre-B cells. These results indicate that initiation of rearrangement is associated with changes in the chromatin structure of both V and J segments, whereas stopping recombination involves changes in only V segment chromatin. We further find an increase in histone H4 acetylation at both the H and kappa L chain loci at the pro-B cell stage. Although histone H4 acetylation appears to be an early change associated with B cell commitment, acetylation alone is not sufficient to promote subsequent modifications in Ig chromatin.
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页码:866 / 874
页数:9
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