Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8456279 | Mutation Research/Genetic Toxicology and Environmental Mutagenesis | 2016 | 8 Pages |
Abstract
DNA double strand breaks induced by AOH due to poisoning of topoisomerase IIα were completely repaired in less than 2 h. Under cell-free conditions, inhibition of topoisomerase IIα could also be measured for ATX II and STTX III at low concentrations, but the perylene quinones were catalytic inhibitors rather than topoisomerase poisons and did not induce DSBs. DNA strand breaks induced by ATX II and STTX III were more persistent and not completely repaired within 24 h. A dependence of the repair rate on the NER status could only be demonstrated for STTX III, resulting in an accumulation of DNA damage in NER-deficient cells. Together with the finding that the DNA glycosylase formamidopyrimidine-DNA glycosylase (Fpg), but not T4 endonuclease V, is able to generate additional DNA strand breaks measurable by the alkaline unwinding assay, we conclude that the genotoxicity of the perylene quinones with an epoxide group is probably caused by the formation of DNA adducts which may be converted to Fpg sensitive sites.
Keywords
FPGDNA single strand breakATX IISSBHprtDSBFCSAMEAOHDMEMPBSapurinic/apyrimidinicDMSONERDulbecco’s modified Eagle mediumalternariolnucleotide excision repairDimethyl sulfoxidefetal calf serumDNA double strand breakFormamidopyrimidine-DNA glycosylasePhosphate buffered salinehypoxanthine guanine phosphoribosyl transferaseplating efficiency
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Authors
Stefanie C. Fleck, Friederike Sauter, Erika Pfeiffer, Manfred Metzler, Andrea Hartwig, Beate Köberle,