The distal V(H) gene cluster of the Igh locus contains distinct regulatory elements with Pax5 transcription factor-dependent activity in pro-B cells

Immunity. 2011 Feb 25;34(2):175-87. doi: 10.1016/j.immuni.2011.02.005.

Abstract

V(H)-DJ(H) recombination of the immunoglobulin heavy chain (Igh) locus is temporally and spatially controlled during early B cell development, and yet no regulatory elements other than the V(H) gene promoters have been identified throughout the entire V(H) gene cluster. Here, we discovered regulatory sequences that are interspersed in the distal V(H) gene region. These conserved repeat elements were characterized by the presence of Pax5 transcription factor-dependent active chromatin by binding of the regulators Pax5, E2A, CTCF, and Rad21, as well as by Pax5-dependent antisense transcription in pro-B cells. The Pax5-activated intergenic repeat (PAIR) elements were no longer bound by Pax5 in pre-B and B cells consistent with the loss of antisense transcription, whereas E2A and CTCF interacted with PAIR elements throughout early B cell development. The pro-B cell-specific and Pax5-dependent activity of the PAIR elements suggests that they are involved in the regulation of distal V(H)-DJ(H) recombination at the Igh locus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / physiology
  • Binding Sites
  • CCCTC-Binding Factor
  • Chromatin / genetics*
  • Chromatin Immunoprecipitation
  • Conserved Sequence
  • DNA, Intergenic / genetics*
  • Gene Rearrangement, B-Lymphocyte, Heavy Chain*
  • Genes, Immunoglobulin / genetics*
  • Immunoglobulin Heavy Chains / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Models, Genetic
  • Oligonucleotide Array Sequence Analysis
  • PAX5 Transcription Factor / deficiency
  • PAX5 Transcription Factor / genetics
  • PAX5 Transcription Factor / physiology*
  • Precursor Cells, B-Lymphoid / metabolism
  • RNA, Antisense / biosynthesis
  • RNA, Antisense / genetics
  • Regulatory Sequences, Nucleic Acid / genetics*
  • Repressor Proteins / physiology
  • Transcription, Genetic

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • CCCTC-Binding Factor
  • Chromatin
  • Ctcf protein, mouse
  • DNA, Intergenic
  • Immunoglobulin Heavy Chains
  • PAX5 Transcription Factor
  • Pax5 protein, mouse
  • RNA, Antisense
  • Repressor Proteins
  • Tcf3 protein, mouse

Associated data

  • GEO/GSE27215