Abstract
Escherichia coli has several overlapping DNA repair pathways which act in concert to eliminate the DNA damage caused by a diverse array of physical and chemical agents. The ABC excinuclease which is encoded by the uvrA, uvrB, and uvrC genes mediates both the incision and excision steps of nucleotide excision repair. Traditionally, this repair pathway has been assumed to be active against DNA adducts that cause major helical distortions. To determine the level of helical deformity required for recognition and repair by ABC excinuclease, we have evaluated the substrate specificity of this enzyme by using DNA damaged by N-methyl-N'-nitro-N-nitrosoguanidine. ABC excinuclease incised methylated DNA in vitro in a dose-dependent manner in a reaction that was ATP dependent and specific for the fully reconstituted enzyme. In vivo studies with various alkylation repair-deficient mutants indicated that the excinuclease participated in the repair of DNA damage induced by N-methyl-N'-nitro-N-nitrosoguanidine.
MeSH Terms
DNA Damage
DNA Repair
Dose-Response Relationship, Drug
Endodeoxyribonucleases/metabolism
Escherichia coli/drug effects,enzymology,genetics
Escherichia coli Proteins
Genotype
Kinetics
Methylnitronitrosoguanidine/pharmacology
Mutation
Species Specificity
Chemicals
Escherichia coli Proteins
Methylnitronitrosoguanidine
Endodeoxyribonucleases
endodeoxyribonuclease uvrABC
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Van Houten B
Sancar A
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