Transcription and recombination of the murine RS element

J Immunol. 1992 Aug 1;149(3):832-40.

Abstract

The deletion of C kappa is a frequent event in lambda-producing B cells in both mice and humans. Deletions of the murine C kappa gene are mediated by recombination events that involve the RS (recombining segment) element located downstream of the C kappa gene. RS recombinations appear to be mediated by the same mechanisms involved in Ig and TCR gene rearrangement. It has been suggested that RS recombinations might activate a factor that is involved in the initiation of lambda gene rearrangement in maturing pre-B cells. We have identified a unique RNA transcript derived from the recombined RS element present in some pre-B cell lines. However, gene transfer studies indicate that this RS transcript is not sufficient to induce lambda gene recombination in pre-B cell lines. We also find that recombination of the RS element in pre-B cell lines is closely correlated with changes in chromatin structure and transcriptional activation. Thus, recombination of the RS element in pre-B cells appears to be regulated in a manner similar to the regulation of antibody gene VDJ joining.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • B-Lymphocytes / physiology*
  • Base Sequence
  • Chromatin / ultrastructure
  • Deoxyribonuclease I / pharmacology
  • Gene Expression Regulation
  • Gene Rearrangement, B-Lymphocyte, Heavy Chain
  • Gene Rearrangement, B-Lymphocyte, Light Chain*
  • Genes, Immunoglobulin*
  • Genes, Switch*
  • Immunoglobulin kappa-Chains / genetics*
  • Immunoglobulin lambda-Chains / genetics*
  • In Vitro Techniques
  • Mice
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides / chemistry
  • RNA, Messenger / genetics
  • Recombination, Genetic*
  • Restriction Mapping

Substances

  • Chromatin
  • Immunoglobulin kappa-Chains
  • Immunoglobulin lambda-Chains
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Deoxyribonuclease I