Targeting of the Sp1 binding sites of HIV-1 long terminal repeat with chromomycin. Disruption of nuclear factor.DNA complexes and inhibition of in vitro transcription

Biochem Pharmacol. 1996 Nov 22;52(10):1489-98. doi: 10.1016/s0006-2952(96)00510-2.

Abstract

Sequence selectivity of DNA-binding drugs has recently been reported in a number of studies employing footprinting and gel retardation approaches. In this paper, we studied the biochemical effects of the sequence-selective binding of chromomycin to the long terminal repeat of the human immunodeficiency type I virus. Deoxyribonuclease I (E.C.3.1.21.1) footprinting, arrested polymerase chain reaction, gel retardation and in vitro transcription experiments have demonstrated that chromomycin preferentially interacts with the binding sites of the promoter-specific transcription factor Sp1. Accordingly, interactions between nuclear proteins and Sp1 binding sites are inhibited by chromomycin, and this effect leads to a sharp inhibition of in vitro transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites / genetics
  • Chromomycins / metabolism*
  • Chromomycins / pharmacology
  • DNA / genetics
  • DNA / metabolism
  • DNA Footprinting
  • DNA Primers / genetics
  • HIV Long Terminal Repeat*
  • HIV-1 / drug effects
  • HIV-1 / genetics*
  • HIV-1 / metabolism*
  • HeLa Cells
  • Humans
  • In Vitro Techniques
  • Jurkat Cells
  • Nuclear Proteins / metabolism
  • Nucleic Acid Synthesis Inhibitors / metabolism*
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Polymerase Chain Reaction
  • Sp1 Transcription Factor / metabolism*
  • Transcription, Genetic / drug effects

Substances

  • Chromomycins
  • DNA Primers
  • Nuclear Proteins
  • Nucleic Acid Synthesis Inhibitors
  • Sp1 Transcription Factor
  • DNA