Schlissel M S, Stanhope-Baker P
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Semin Immunol. 1997 Jun;9(3):161-70. doi: 10.1006/smim.1997.0066.
Antigen receptor genes are assembled from their component gene segments by a highly regulated series of site-specific DNA recombination reactions known as V(D)J recombination. Proteins encoded by the RAG1 and RAG2 genes are responsible for the recognition and double-stranded cleavage of a highly conserved DNA sequence flanking all rearranging gene segments. It remains uncertain how this common lymphoid recombinase is targeted to distinct loci in developing B and T cells and to specific loci at successive stages of lymphocyte development. This review considers evidence that DNA sequences which regulate the transcription of antigen receptor genes also regulate the recombination reaction by determining the accessibility of individual loci to the V(D)J recombinase.
抗原受体基因通过一系列高度调控的位点特异性DNA重组反应(称为V(D)J重组),由其组成基因片段组装而成。RAG1和RAG2基因编码的蛋白质负责识别和双链切割所有重排基因片段侧翼的高度保守DNA序列。目前尚不清楚这种常见的淋巴细胞重组酶如何在发育中的B细胞和T细胞中靶向不同的基因座,以及在淋巴细胞发育的连续阶段靶向特定基因座。本综述探讨了相关证据,即调节抗原受体基因转录的DNA序列也通过决定各个基因座对V(D)J重组酶的可及性来调节重组反应。