Congenital defects in V(D)J recombination

Br Med Bull. 2015 Jun;114(1):157-67. doi: 10.1093/bmb/ldv020. Epub 2015 May 17.

Abstract

Introduction or background: The V(D)J recombination is a DNA rearrangement process that generates the diversity of T and B lymphocyte immune repertoire. It proceeds through the generation of a DNA double-strand break (DNA-DSB) by the Rag1/2 lymphoid-specific factors, which is repaired by the non-homologous end joining (NHEJ) DNA repair pathway. V(D)J recombination also constitutes a checkpoint in the lymphoid development.

Sources of data: V(D)J recombination defect results in severe combined immune deficiency (SCID) with a lack of T and B lymphocytes.

Areas of agreement: The V(D)J recombination represents one of the few programmed molecular events leading to DNA-DSBs that strictly relies on NHEJ. Two NHEJ factors, Artemis and XLF/Cernunnos, were identified through the molecular studies of SCID patients. Mutations in PRKDC and DNA Ligase IV genes also result in SCID.

Growing points: Studies in mice have demonstrated that XLF/Cernunnos is dispensable for V(D)J recombination in lymphoid cells but not for the repair of genotoxic-induced DNA-DSBs, which raises the question of the implication of Rag1/2 factors in the DNA repair phase of V(D)J recombination.

Areas timely for developing research: New factors of NHEJ, such as PAXX, are being identified. Patients with NHEJ deficiency (XRCC4) without immune deficiency were recently reported. We, therefore, may not have yet the complete picture of DNA-DSB repair in the context of V(D)J recombination.

Keywords: DNA repair; NHEJ; V(D)J recombination; lymphocyte development; severe combined immune deficiency.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Congenital Abnormalities / genetics*
  • Congenital Abnormalities / immunology
  • DNA End-Joining Repair
  • DNA-Binding Proteins / genetics
  • Genes, RAG-1
  • Humans
  • Lymphocyte Subsets / immunology
  • Nuclear Proteins / genetics
  • Severe Combined Immunodeficiency / genetics*
  • Severe Combined Immunodeficiency / immunology
  • V(D)J Recombination*

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • RAG2 protein, human