NF-κB and BRG1 bind a distal regulatory element in the IL-3/GM-CSF locus

Mol Immunol. 2011 Sep;48(15-16):2178-88. doi: 10.1016/j.molimm.2011.07.016. Epub 2011 Aug 9.

Abstract

We investigated gene regulation at the IL-3/GM-CSF gene cluster. We found BRG1, a SWI/SNF remodeling ATPase, bound a distal element, CNSa. BRG1 binding was strongest in differentiated, stimulated T helper cells, paralleling IL-3 and GM-CSF expression. Depletion of BRG1 reduced IL-3 and GM-CSF transcription. BAF-specific SWI/SNF subunits bound to this locus and regulated IL-3 expression. CNSa was in closed chromatin in fibroblasts, open chromatin in differentiated T helper cells, and moderately open chromatin in naïve (undifferentiated) T helper cells; BRG1 was required for the most open state. CNSa increased transcription of a reporter in an episomal expression system, in a BRG1-dependent manner. The NF-κB subunit RelA/p65 bound CNSa in activated T helper cells. Inhibition of NF-κB blocked BRG1 binding to CNSa, chromatin opening at CNSa, and activation of IL-3 and GM-CSF. Together, these findings suggest CNSa is a distal enhancer that binds BRG1 and NF-κB.

Publication types

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

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromatin Immunoprecipitation
  • DNA Helicases / genetics*
  • DNA Helicases / immunology
  • DNA Helicases / metabolism
  • Gene Expression
  • Gene Expression Regulation / genetics*
  • Gene Expression Regulation / immunology
  • Immunoblotting
  • Interleukin-3 / genetics*
  • Interleukin-3 / immunology
  • Interleukin-3 / metabolism
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B / genetics*
  • NF-kappa B / immunology
  • NF-kappa B / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / immunology
  • Nuclear Proteins / metabolism
  • Polymerase Chain Reaction
  • Regulatory Elements, Transcriptional / genetics*
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / immunology
  • Transcription Factors / metabolism
  • Transduction, Genetic

Substances

  • Interleukin-3
  • NF-kappa B
  • Nuclear Proteins
  • Transcription Factors
  • Smarca4 protein, mouse
  • DNA Helicases