The 4-nitroquinoline 1-oxide mutational spectrum in single stranded DNA is characterized by guanine to pyrimidine transversions

Nucleic Acids Res. 1992 Mar 25;20(6):1283-7. doi: 10.1093/nar/20.6.1283.

Abstract

4-Nitroquinoline-1-oxide is a potent mutagen and carcinogen which induces two main guanine adducts at positions C8 and N2. In ds or ss damaged DNA the ratio C8/N2 adducts is 1:2 and 8-10:1, respectively. In bacteria and yeast 4NQO has been shown to be a base substitution mutagen acting at G residues inducing mainly G to A transitions. We determined the mutational spectrum induced by the 4NQO metabolite, acetoxy-4-aminoquinoline 1-oxide, in the M13lacZ'/E. coli lacZ delta M15 alpha complementation assay using ssDNA. Among 68 Ac-4HAQO induced mutants, G to Pyr transversion was the most frequent base substitution observed. By comparison with dsDNA based systems, our data suggest that dGuo-C8-AQO induces G to Pyr transversions. A mechanism to explain how this lesion may induce transversions is proposed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Nitroquinoline-1-oxide / pharmacology*
  • Base Sequence
  • DNA Damage
  • DNA Mutational Analysis
  • DNA Repair
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / drug effects
  • DNA, Single-Stranded / chemistry
  • DNA, Single-Stranded / drug effects*
  • Escherichia coli / genetics
  • Guanine / chemistry
  • Molecular Sequence Data
  • Pyrimidines / chemistry
  • Transfection

Substances

  • DNA, Bacterial
  • DNA, Single-Stranded
  • Pyrimidines
  • 4-Nitroquinoline-1-oxide
  • Guanine