Recombination activating gene and its defects

Curr Opin Allergy Clin Immunol. 2001 Dec;1(6):491-5. doi: 10.1097/00130832-200112000-00001.

Abstract

Mutations in recombination activating genes cause a spectrum of severe immunodeficiencies ranging from T-B severe combined immunodeficiency to Omenn syndrome (a particular type of severe combined immunodeficiency presenting a T+ B- profile). Although environmental factors and genetic background could also contribute to the genesis of this pathological condition, a residual recombination activating gene activity allowing for a few recombinational events to occur, is the first determinant of this variability in the clinical picture.

Publication types

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

MeSH terms

  • DNA Nucleotidyltransferases / genetics
  • DNA-Binding Proteins / genetics*
  • Gene Expression Regulation
  • Genes, RAG-1*
  • Humans
  • Mutation
  • Nuclear Proteins
  • Severe Combined Immunodeficiency / genetics*
  • Syndrome
  • VDJ Recombinases

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • RAG2 protein, human
  • V(D)J recombination activating protein 2
  • DNA Nucleotidyltransferases
  • VDJ Recombinases