Proceedings of the National Academy of Sciences · 1997 · 354 citations · 21 references
Life SciencesGeneticsMolecular BiologyDna RepairEnzymologyGene ExpressionBase Excision RepairDna DamageDna Double-strand Break RepairDna Repair In CarcinogenesisDna Strand BreaksDouble-strand Break Repair8-Oxo-7, 8-DihydroguanineBase Excision Repair CleavageCdna CloningCdna SynthesisDna Repair PathwaysMutagenic MechanismsMutator PhenotypesYeast Dna Repair
The major mutagenic base lesion in DNA caused by exposure to reactive oxygen species is 8-hydroxyguanine (8-oxo-7, 8-dihydroguanine). In bacteria and Saccharomyces cerevisiae, this damaged base is excised by a DNA glycosylase with an associated lyase activity for chain cleavage. We have cloned, sequenced, and expressed a human cDNA with partial sequence homology to the relevant yeast gene. The encoded 47-kDa human enzyme releases free 8-hydroxyguanine from oxidized DNA and introduces a chain break in a double-stranded oligonucleotide specifically at an 8-hydroxyguanine residue base paired with cytosine. Expression of the human protein in a DNA repair-deficient E. coli mutM mutY strain partly suppresses its spontaneous mutator phenotype. The gene encoding the human enzyme maps to chromosome 3p25. These results show that human cells have an enzyme that can initiate base excision repair at mutagenic DNA lesions caused by active oxygen.
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