Germline transcription from T-cell receptor Vbeta gene is uncoupled from allelic exclusion

EMBO J. 2007 May 2;26(9):2387-99. doi: 10.1038/sj.emboj.7601671. Epub 2007 Apr 5.

Abstract

Allelic exclusion operates in B and T lymphocytes to ensure clonal expression of antigen receptors after V(D)J recombination. Germline transcription, which proceeds V(D)J recombination, has been postulated to provide an instructive signal for allelic exclusion. Here, we use a genetic marker to track germline transcription from a Vbeta gene within the TCRbeta locus. We find that developing thymocytes exhibit uniformed, bi-allelic activation of the Vbeta gene before V-DJ recombination, a process subject to allelic exclusion. We further show that V-DJ rearrangement promotes activation rather than silencing of germline transcription from the remaining Vbeta genes on either the functionally or non-functionally rearranged chromosome. Results presented here suggest that germline transcription, although necessary for V(D)J recombination, is not sufficient to instruct allelic exclusion.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Animals
  • CD2 Antigens / metabolism
  • Embryonic Stem Cells / metabolism
  • Gene Rearrangement, beta-Chain T-Cell Antigen Receptor*
  • Gene Silencing
  • Genetic Markers
  • Humans
  • Mice
  • Mice, Mutant Strains
  • Peptide Fragments / biosynthesis*
  • Peptide Fragments / genetics
  • Receptors, Antigen, T-Cell, alpha-beta / biosynthesis*
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Recombination, Genetic*
  • T-Lymphocytes / metabolism*
  • Transcriptional Activation*

Substances

  • CD2 Antigens
  • Genetic Markers
  • Peptide Fragments
  • Receptors, Antigen, T-Cell, alpha-beta
  • T-cell receptor Vbeta 8.2