Mechanisms for feedback inhibition of the immunoglobulin heavy chain locus

Curr Opin Immunol. 2004 Apr;16(2):235-40. doi: 10.1016/j.coi.2004.02.003.

Abstract

The production of immunoglobulin heavy chain (IgH) protein in pro-B cells provides feedback to terminate further V(H) gene recombination. This phenomenon is referred to as allelic exclusion. The chromatin structure of the V(H) genes regulates their recombination potential, hence alterations in chromatin are a key factor in allelic exclusion. In pro-B cells, IL-7/IL-7R signaling induces histone hyperacetylation and nuclease accessibility of the largest family of V(H) genes (J558) and potentially activates these genes for recombination. Loss of these signals in the later stages of B-cell development reverts the V(H)J558 gene segments to a less accessible state, making them recombinationally refractive. This provides a molecular mechanism for allelic exclusion of these genes. Similar transient signals may be responsible for enforcing allelic exclusion in other V(H) gene families. D-proximal V(H) genes, however, appear to be less susceptible to feedback inhibition.

Publication types

  • Review

MeSH terms

  • Alleles*
  • Animals
  • Cell Division
  • Feedback, Physiological*
  • Genes, Immunoglobulin*
  • Immunoglobulin Heavy Chains / genetics*
  • Immunoglobulin Heavy Chains / metabolism
  • Immunoglobulin Variable Region / metabolism
  • Interleukin-7 / genetics
  • Interleukin-7 / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Signal Transduction

Substances

  • Immunoglobulin Heavy Chains
  • Immunoglobulin Variable Region
  • Interleukin-7