Sen Ranjan, Oltz Eugene
Laboratory of Cellular and Molecular Biology, National Institute on Aging/National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
Curr Opin Immunol. 2006 Jun;18(3):237-42. doi: 10.1016/j.coi.2006.03.008. Epub 2006 Apr 17.
Precursor B cells assemble a diverse repertoire of immunoglobulin (Ig) genes by the process of V(D)J recombination. Assembly of IgH genes is regulated in a tissue- and stage-specific manner via the activation and then the inactivation of distinct regions within the one megabase IgH locus. Recent studies have shown that regional control is achieved using a combination of genetic and epigenetic strategies, which modulate chromatin accessibility to V(D)J recombinase, relocate IgH loci within the nucleus, and promote changes in locus conformation that alter the spatial proximity of target gene segments. Orchestration of these regulatory processes is crucial for the generation of a functional B cell repertoire.
前体B细胞通过V(D)J重组过程组装出多样化的免疫球蛋白(Ig)基因库。IgH基因的组装通过一个百万碱基对的IgH基因座内不同区域的激活和随后的失活,以组织和阶段特异性的方式进行调控。最近的研究表明,区域控制是通过遗传和表观遗传策略的组合实现的,这些策略调节染色质对V(D)J重组酶的可及性,将IgH基因座重新定位到细胞核内,并促进基因座构象的变化,从而改变靶基因片段的空间邻近性。这些调控过程的协调对于功能性B细胞库的产生至关重要。