Department of Immunobiology and Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06520-8011, USA.
Annu Rev Genet. 2011;45:167-202. doi: 10.1146/annurev-genet-110410-132552. Epub 2011 Aug 19.
V(D)J recombination assembles immunoglobulin and T cell receptor genes during lymphocyte development through a series of carefully orchestrated 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.
V(D)J 重组通过一系列精心协调的 DNA 断裂和连接事件,在淋巴细胞发育过程中组装免疫球蛋白和 T 细胞受体基因。DNA 切割需要一系列含有 RAG1 和 RAG2 蛋白以及侧翼重组基因片段的重组信号的蛋白-DNA 复合物。在这篇综述中,我们讨论了我们对 RAG 蛋白的功能和结构组织、RAG-DNA 复合物的组成和结构以及导致这些复合物形成的途径的理解的最新进展。我们还考虑了 RAG 介导的组蛋白识别和泛素连接酶活性的功能意义,以及 RAG 在确保 V(D)J 重组过程中产生的 DNA 断裂正确修复中的作用。最后,我们提出了一个 RAG-DNA 复合物形成的模型,该模型涉及 RAG1 在重组信号非七聚体上的锚定和 RAG2 依赖性监视相邻 DNA 中合适的间隔子和七聚体序列。