Sleckman Barry P
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Immunol Res. 2005;32(1-3):253-8. doi: 10.1385/IR:32:1-3:253.
Lymphocyte antigen receptor genes are assembled through the cutting and joining of segments of DNA in developing lymphocytes. The basic features of the biochemical steps of this assembly process, referred to as the V(D)J recombination, are similar for the assembly of all lymphocyte antigen receptor genes, yet this assembly is precisely regulated in several important contexts during lymphocyte development. It has long been appreciated that this occurs through modulation of accessibility of antigen receptor loci to the enzymatic complex that assembles antigen receptor genes. However, recent studies have suggested that some regulatory constraints may be enforced at the level of the V(D)J recombination reaction itself. This review focuses on recent advances in the understanding of the regulation of antigen receptor gene assembly, with particular attention paid to the assembly of T-cell receptor beta-chain genes during T-cell development.
淋巴细胞抗原受体基因是通过发育中的淋巴细胞中DNA片段的切割和连接来组装的。这个组装过程的生化步骤的基本特征,即V(D)J重组,对于所有淋巴细胞抗原受体基因的组装都是相似的,然而在淋巴细胞发育过程中的几个重要情况下,这种组装受到精确调控。长期以来人们认识到,这是通过调节抗原受体基因座对组装抗原受体基因的酶复合物的可及性来实现的。然而,最近的研究表明,一些调控限制可能在V(D)J重组反应本身的水平上实施。本综述重点关注抗原受体基因组装调控理解方面的最新进展,特别关注T细胞发育过程中T细胞受体β链基因的组装。