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Nucleic Acids Res. 2005 Sep 20;33(16):5094-105. Print 2005.

8-oxoguanine incorporation into DNA repeats in vitro and mismatch recognition by MutSalpha.

Author information

1
Cancer Research UK London Research Institute, Clare Hall Laboratories South Mimms, Herts, EN6 3LD, UK.

Erratum in

  • Nucleic Acids Res. 2005;33(18):6081.

Abstract

DNA 8-oxoguanine (8-oxoG) causes transversions and is also implicated in frameshifts. We previously identified the dNTP pool as a likely source of mutagenic DNA 8-oxoG and demonstrated that DNA mismatch repair prevented oxidation-related frameshifts in mononucleotide repeats. Here, we show that both Klenow fragment and DNA polymerase alpha can utilize 8-oxodGTP and incorporate the oxidized purine into model frameshift targets. Both polymerases incorporated 8-oxodGMP opposite C and A in repetitive DNA sequences and efficiently extended a terminal 8-oxoG. The human MutSalpha mismatch repair factor recognized DNA 8-oxoG efficiently in some contexts that resembled frameshift intermediates in the same C or A repeats. DNA 8-oxoG in other slipped/mispaired structures in the same repeats adopted configurations that prevented recognition by MutSalpha and by the OGG1 DNA glycosylase thereby rendering it invisible to DNA repair. These findings are consistent with a contribution of oxidative DNA damage to frameshifts. They also suggest how mismatch repair might reduce the burden of DNA 8-oxoG and prevent frameshift formation.

PMID:
16174844
PMCID:
PMC1233161
DOI:
10.1093/nar/gki813
[Indexed for MEDLINE]
Free PMC Article

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