NF-kappa B-mediated chromatin reconfiguration and transcriptional activation of the HIV-1 enhancer in vitro

Genes Dev. 1996 Jan 1;10(1):37-49. doi: 10.1101/gad.10.1.37.

Abstract

NF-kappa B is a potent inducible transcription factor that regulates many genes in activated T cells. In this report we examined the ability of different subunits of NF-kappa B to enhance HIV-1 transcription in vitro with chromatin templates. We find that the p65 subunit of NF-kappa B is a strong transcriptional activator of nucleosome-assembled HIV-1 DNA, whereas p50 does not activate transcription, and that p65 activates transcription synergistically with Sp1 and distal HIV-1 enhancer-binding factors (LEF-1, Ets-1, and TFE-3). These effects were observed with chromatin, but not with nonchromatin templates. Furthermore, binding of either p50 or p65 with Sp1 induces rearrangement of the chromatin to a structure that resembles the one reported previously for integrated HIV-1 proviral DNA in vivo. These results suggest that p50 and Sp1 contribute to the establishment of the nucleosomal arrangement of the uninduced provirus in resting T cells, and that p65 activates transcription by recruitment of the RNA polymerase II transcriptional machinery to the chromatin-repressed basal promoter.

Publication types

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

MeSH terms

  • Base Sequence
  • Binding Sites
  • Chromatin / chemistry
  • Chromatin / genetics*
  • Chromatin / metabolism
  • DNA-Binding Proteins / genetics
  • Gene Expression Regulation, Viral*
  • HIV Enhancer / genetics*
  • HIV Long Terminal Repeat
  • HeLa Cells
  • Humans
  • Lymphoid Enhancer-Binding Factor 1
  • Molecular Sequence Data
  • NF-kappa B / chemistry
  • NF-kappa B / genetics*
  • NF-kappa B / isolation & purification
  • NF-kappa B / metabolism
  • NF-kappa B p50 Subunit
  • Nucleosomes / genetics
  • Repetitive Sequences, Nucleic Acid
  • Sp1 Transcription Factor / genetics
  • Sp1 Transcription Factor / metabolism
  • Trans-Activators
  • Transcription Factor RelA
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic*

Substances

  • Chromatin
  • DNA-Binding Proteins
  • LEF1 protein, human
  • Lymphoid Enhancer-Binding Factor 1
  • NF-kappa B
  • NF-kappa B p50 Subunit
  • Nucleosomes
  • Sp1 Transcription Factor
  • Trans-Activators
  • Transcription Factor RelA
  • Transcription Factors