V(D)J Recombination: Mechanisms of Initiation

被引:377
作者
Schatz, David G. [1 ,2 ]
Swanson, Patrick C. [3 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[3] Creighton Univ, Dept Med Microbiol & Immunol, Med Ctr, Omaha, NE 68178 USA
来源
ANNUAL REVIEW OF GENETICS, VOL 45 | 2011年 / 45卷
关键词
site-specific recombination; recombination signal sequence; RAG1; RAG2; HMGB1; protein-DNA complex; SUPPRESSES GENOMIC INSTABILITY; RAG1/RAG2 SYNAPTIC COMPLEX; CRITICAL CONTROL POINT; DNA HAIRPIN FORMATION; AMINO-ACID-RESIDUES; N-TERMINAL DOMAIN; SIGNAL SEQUENCE; HISTONE H3; UBIQUITIN LIGASE; 12/23; RULE;
D O I
10.1146/annurev-genet-110410-132552
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
V(D)J recombination assembles immunoglobulin and T cell receptor genes during lymphocyte development through a series of carefully or-chestrated DNA breakage and rejoining events. DNA cleavage requires a series of protein-DNA complexes containing the RAG1 and RAG2 proteins and recombination signals that flank the recombining gene segments. In this review, we discuss recent advances in our understanding of the function and domain organization of the RAG proteins, the composition and structure of RAG-DNA complexes, and the pathways that lead to the formation of these complexes. We also consider the functional significance of RAG-mediated histone recognition and ubiquitin ligase activities, and the role played by RAG in ensuring proper repair of DNA breaks made during V(D)J recombination. Finally, we propose a model for the formation of RAG-DNA complexes that involves anchoring of RAG1 at the recombination signal nonamer and RAG2-dependent surveillance of adjoining DNA for suitable spacer and heptamer sequences.
引用
收藏
页码:167 / 202
页数:36
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