Mutagenic effects of 2-hydroxy-dATP on replication in a HeLa extract: induction of substitution and deletion mutations

Nucleic Acids Res. 2003 May 15;31(10):2570-5. doi: 10.1093/nar/gkg368.

Abstract

The mutagenicity of an oxidized form of dATP, 2-hydroxydeoxyadenosine 5'-triphosphate (2-OH-dATP), was examined using an SV40 origin-dependent in vitro replication system with a HeLa extract. 2-OH-dATP induced mutations in a dose-dependent manner and elicited substitution and deletion mutations. Of the substitutions, a G.C-->A.T transition including a tandem (CC-->TT) mutation was mainly observed. This result agrees with our previous observation that mammalian DNA polymerase alpha misincorporates the oxidized nucleotide opposite C, but is in contrast to the finding that 2-OH-dATP elicits G.C-->T.A transversions in Escherichia coli. This type of mutation was also elicited, but to a lesser extent. Interestingly, the mutagenicity of 2-OH-dATP was enhanced in the presence of 2-hydroxydeoxyadenosine 5'-diphosphate, an inhibitor of the MTH1 protein, suggesting that this protein functions in the hydrolysis of 2-OH-dATP in the replication reaction mixture, and probably in living cells. These results indicate that 2-OH-dATP is mutagenic and that its mutagenicity is suppressed by the MTH1 protein in mammalian cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / analogs & derivatives
  • Adenosine Triphosphate / pharmacology*
  • Base Sequence
  • Cell Extracts
  • DNA Replication / drug effects*
  • DNA Replication / genetics
  • Genes, Suppressor
  • HeLa Cells
  • Humans
  • Models, Genetic
  • Molecular Sequence Data
  • Mutagenesis / drug effects
  • Mutagens / pharmacology*
  • Point Mutation / drug effects
  • RNA, Transfer / genetics
  • Sequence Analysis, DNA
  • Sequence Deletion

Substances

  • Cell Extracts
  • Mutagens
  • supF tRNA
  • Adenosine Triphosphate
  • RNA, Transfer