Mutation spectra induced by 1-nitropyrene 4,5-oxide and 1-nitropyrene 9,10-oxide in the supF gene of human XP-A fibroblasts

BMB Rep. 2008 Aug 31;41(8):604-8. doi: 10.5483/bmbrep.2008.41.8.604.

Abstract

1-Nitropyrene 4,5-oxide and 1-nitropyrene 9,10-oxide are oxidative metabolites that are responsible for the mutagenicity of 1-nitropyrene. In this study, the mutation spectra induced by oxidative metabolites in human cells were determined using a shuttle vector assay. The mutation frequencies induced by 1-nitropyrene 9,10-oxide were 2-3 times higher than those induced by 1-nitropyrene 4,5-oxide. The base substitutions induced by 1-nitropyrene 4,5-oxide were G --> A transitions, G --> C transversions, and G --> T transversions. In the case of 1-nitropyrene 9,10-oxide, G --> A transitions, G --> T transversions, A --> G transitions and G --> C transversions were observed. Most base substitution mutations induced by oxidative metabolites occurred at the guanine sites in the supF gene. These sequence-specific hot spots were commonly identified as 5'-GA sequences for both metabolites. On the other hand, the sequence-specific hot spots at the adenine sites were identified as 5'-CAC sequences for 1-nitropyrene 9,10-oxide. These results suggest that the oxidative metabolites of 1-nitropyrene induce sequence-specific DNA mutations at the guanine and adenine sites at high frequency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Line, Transformed
  • DNA / genetics
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Genes, Suppressor
  • Genetic Vectors
  • Humans
  • Molecular Sequence Data
  • Mutagens / toxicity
  • Mutation*
  • Plasmids / genetics
  • Pyrenes / toxicity*
  • RNA, Transfer / genetics*
  • Xeroderma Pigmentosum / genetics*
  • Xeroderma Pigmentosum Group A Protein / genetics*

Substances

  • Mutagens
  • Pyrenes
  • XPA protein, human
  • Xeroderma Pigmentosum Group A Protein
  • supF tRNA
  • 1-nitropyrene-4,5-oxide
  • 1-nitropyrene-9,10-oxide
  • DNA
  • RNA, Transfer