Journal of the American Chemical Society · 2013 · 34 citations · 16 references
Life SciencesBiochemistryMolecular BiologyEnzymologyNucleic Acid BiochemistryNucleic Acid ChemistryBase StackingDna Polymerase FunctionError-prone MutagenesisOligonucleotide ChemistryPolymerase Chain ReactionReplication FidelityBase Pair GeometryBase Pair MismatchesCatalytic EfficiencyDna Polymerase ChemistryDna Polymerase FidelityDna Polymerase SelectivityError-prone Polymerase Chain ReactionPrimer Extension
The influence of base pair size and shape on the fidelity of DNA polymerase-mediated extension past lesion-containing mispairs was examined. Primer extension analysis was performed with synthetic nucleosides paired opposite the pro-mutagenic DNA lesion O(6)-benzylguanine (O(6)-BnG). These data indicate that the error-prone DNA polymerase IV (Dpo4) inefficiently extended past the larger Peri:O(6)-BnG base pair, and in contrast, error-free extension was observed for the smaller BIM:O(6)-BnG base pair. Steady-state kinetic analysis revealed that Dpo4 catalytic efficiency was strongly influenced by the primer:template base pair. Compared to the C:G pair, a 1.9- and 79,000-fold reduction in Dpo4 efficiency was observed for terminal C:O(6)-BnG and BIM:G base pairs respectively. These results demonstrate the impact of geometrical size and shape on polymerase-mediated mispair extension.
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