Jung David, Giallourakis Cosmas, Mostoslavsky Raul, Alt Frederick W
Howard Hughes Medical Institute, Children's Hospital, CBR Institute for Biomedical Research, and Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Annu Rev Immunol. 2006;24:541-70. doi: 10.1146/annurev.immunol.23.021704.115830.
V(D)J recombination assembles antigen receptor variable region genes from component germline variable (V), diversity (D), and joining (J) gene segments. For B cells, such rearrangements lead to the production of immunoglobulin (Ig) proteins composed of heavy and light chains. V(D)J is tightly controlled at the Ig heavy chain locus (IgH) at several different levels, including cell-type specificity, intra- and interlocus ordering, and allelic exclusion. Such controls are mediated at the level of gene segment accessibility to V(D)J recombinase activity. Although much has been learned, many long-standing questions regarding the regulation of IgH locus rearrangements remain to be elucidated. In this review, we summarize advances that have been made in understanding how V(D)J recombination at the IgH locus is controlled and discuss important areas for future investigation.
V(D)J重排从组成性种系可变(V)、多样性(D)和连接(J)基因片段组装抗原受体可变区基因。对于B细胞,此类重排导致产生由重链和轻链组成的免疫球蛋白(Ig)蛋白。V(D)J在免疫球蛋白重链基因座(IgH)受到多个不同水平的严格控制,包括细胞类型特异性、基因座内和基因座间排序以及等位基因排斥。此类控制在基因片段对V(D)J重组酶活性的可及性水平上介导。尽管已经了解了很多,但关于IgH基因座重排调控的许多长期存在的问题仍有待阐明。在本综述中,我们总结了在理解IgH基因座处的V(D)J重排如何受到控制方面所取得的进展,并讨论了未来研究的重要领域。