4.6 Review Book Chapter

V(D)J Recombination: Mechanisms of Initiation

Journal

ANNUAL REVIEW OF GENETICS, VOL 45
Volume 45, Issue -, Pages 167-202

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-genet-110410-132552

Keywords

site-specific recombination; recombination signal sequence; RAG1; RAG2; HMGB1; protein-DNA complex

Funding

  1. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R37AI032524, R56AI055599] Funding Source: NIH RePORTER
  2. Howard Hughes Medical Institute Funding Source: Medline
  3. NIAID NIH HHS [R37 AI032524, 3R56 AI055599-06A1S1, R37 AI32524] Funding Source: Medline

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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.

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