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DNA Repair (Amst) ; 2(2): 159-73, 2003 Feb 03.
Article in English | MEDLINE | ID: mdl-12531387

ABSTRACT

We have investigated in detail the interactions between the Escherichia coli mutT, mutM, and mutY error-prevention systems. Jointly, these systems protect the cell against the effects of the oxidative stress product, 8-oxoguanine (8-oxoG), a base analog with ambiguous base-pairing properties, pairing with either A or C during DNA synthesis. mutT mutator strains display a specific increase in A.T-->C.G transversions, while mutM and mutY mutator strains show specific G.C-->T.A increases. To study in more detail the in vivo processing of the various mutational intermediates leading to A.T-->C.G and G.C-->T.A transversions, we analyzed defined A.T-->C.G and G.C-->T.A events in strains containing all possible combinations of these mutator alleles. We report three major findings. First, we do not find evidence that the mutT allele significantly increases G.C-->T.A transversions in either mut(+), mutM, mutY or mutMmutY backgrounds. We interpret this result to indicate that incorporation of 8-oxodGTP opposite template C may not be frequent relative to incorporation opposite template A. Second, we show that mutT-induced A.T-->C.G transversions are significantly reduced in strains carrying mutY and mutMmutY deficiencies suggesting that 8-oxoG, when present in DNA, preferentially mispairs with dATP. Third, the mutY and mutMmutY deficiencies also decrease A.T-->C.G transversions in the mutT(+) background, suggesting that, even in the presence of functional MutT protein, A.T-->C.G transversions may still result from 8-oxodGTP misincorporation.


Subject(s)
DNA Glycosylases , DNA Repair/physiology , Escherichia coli Proteins/metabolism , Escherichia coli/metabolism , N-Glycosyl Hydrolases/metabolism , Phosphoric Monoester Hydrolases/metabolism , DNA Repair/genetics , DNA-Formamidopyrimidine Glycosylase , Drug Resistance, Bacterial/genetics , Escherichia coli/genetics , Escherichia coli Proteins/genetics , Lac Operon/genetics , N-Glycosyl Hydrolases/genetics , Phosphoric Monoester Hydrolases/genetics , Pyrophosphatases
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