Epigenetic ontogeny of the Igk locus during B cell development

被引:136
作者
Goldmit, M
Ji, YH
Skok, J
Roldan, E
Jung, S
Cedar, H
Bergman, Y [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Dept Expt Med, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Sch Med, Dept Cellular Biochem, IL-91120 Jerusalem, Israel
[3] UCL, Dept Immunol & Mol Pathol, London W1T 4JF, England
[4] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
基金
美国国家卫生研究院; 英国惠康基金;
关键词
D O I
10.1038/ni1154
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To become accessible for rearrangement, the immunoglobulin kappa locus must undergo a series of epigenetic changes. This begins in pro-B cells with the relocation of both immunoglobulin kappa alleles from the periphery to the center of the nucleus. In pre-B cells, one allele became preferentially packaged into an active chromatin structure characterized by histone acetylation and methylation of histone H3 lysine 4, while the other allele was recruited to heterochromatin, where it was associated with heterochromatin protein-gamma and Ikaros. These events in cis made only one allele accessible to trans-acting factors, such as RelB, which mediated DNA demethylation, to facilitate rearrangement. These results suggest that early B lymphoid epigenetic changes generate differential structures that serve as the basis for allelic exclusion.
引用
收藏
页码:198 / 203
页数:6
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