Triple helices formed at oligopyrimidine*oligopurine sequences with base pair inversions: effect of a triplex-specific ligand on stability and selectivity

Nucleic Acids Res. 1998 May 1;26(9):2179-83. doi: 10.1093/nar/26.9.2179.

Abstract

Oligonucleotide-directed triple helix formation is mostly restricted to oligopyrimidine*oligopurine sequences of double helical DNA. An interruption of one or two pyrimidines in the oligopurine target strand leads to a strong triplex destabilisation. We have investigated the effect of nucleotide analogues introduced in the third strand at the site opposite the base pair inversion(s). We show that a 3-nitropyrrole derivative (M) discriminates G*C from C*G, A*T and T*A in the presence of a triplex-specific ligand (a benzo[e]pyridoindole derivative, BePI). N6-methoxy-2,6-diaminopurine (K) binds to an A*T base pair better than a T*A, G*C or C*G base pair. Some discrimination is still observed in the presence of BePI and triplex stability is markedly increased. These findings should help in designing BePI-oligonucleotide conjugates to extend the range of DNA sequences available for triplex formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Inversion
  • DNA / chemistry*
  • DNA / drug effects
  • Hydrogen Bonding
  • Indoles / pharmacology
  • Ligands
  • Nucleic Acid Conformation*
  • Oligonucleotides
  • Purines
  • Pyridines / pharmacology
  • Pyrimidines

Substances

  • Indoles
  • Ligands
  • Oligonucleotides
  • Purines
  • Pyridines
  • Pyrimidines
  • triplex DNA
  • 3-methoxy-7H-8-methyl-11-((3'-amino)propylamino)benzo(e)pyrido(4,3-b)indole
  • DNA