Artemis sheds new light on V(D)J recombination

Immunol Rev. 2004 Aug:200:142-55. doi: 10.1111/j.0105-2896.2004.00169.x.

Abstract

V(D)J recombination represents one of the three mechanisms that contribute to the diversity of the immune repertoire of B lymphocytes and T lymphocytes. It also constitutes a major checkpoint during the development of the immune system. Indeed, any V(D)J recombination deficiency leads to a block of B-cell and T-cell maturation in humans and animal models, leading to severe combined immunodeficiency (T-B-SCID). Nine factors have been identified so far to participate in V(D)J recombination. The discovery of Artemis, mutated in a subset of T-B-SCID, provided some new information regarding one of the missing V(D)J recombinase activities: hairpin opening at coding ends prior to DNA repair of the recombination activating genes 1/2-generated DNA double-strand break. New conditions of immune deficiency in humans are now under investigations and should lead to the identification of additional V(D)J recombination/DNA repair factors.

Publication types

  • Review

MeSH terms

  • DNA Repair*
  • DNA-Binding Proteins / genetics
  • Endonucleases
  • Gene Rearrangement, B-Lymphocyte / physiology*
  • Gene Rearrangement, T-Lymphocyte / physiology*
  • Homeodomain Proteins / genetics
  • Humans
  • Immune System Diseases / enzymology
  • Nuclear Proteins / immunology
  • Nuclear Proteins / physiology*
  • Recombination, Genetic
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • beta-Lactamases / immunology
  • beta-Lactamases / physiology

Substances

  • DNA-Binding Proteins
  • Homeodomain Proteins
  • Nuclear Proteins
  • RAG2 protein, human
  • V(D)J recombination activating protein 2
  • RAG-1 protein
  • DCLRE1C protein, human
  • Endonucleases
  • beta-Lactamases