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dc.contributor.authorKlungland, Aen
dc.contributor.authorFairbairn, Leslie Jen
dc.contributor.authorWatson, Amanda Jen
dc.contributor.authorMargison, Geoffrey Pen
dc.contributor.authorSeeberg, Een
dc.date.accessioned2010-08-02T16:16:26Z
dc.date.available2010-08-02T16:16:26Z
dc.date.issued1992-12
dc.identifier.citationExpression of the E.coli 3-methyladenine DNA glycosylase I gene in mammalian cells reduces the toxic and mutagenic effects of methylating agents. 1992, 11 (12):4439-44 EMBO J.en
dc.identifier.issn0261-4189
dc.identifier.pmid1425578
dc.identifier.urihttp://hdl.handle.net/10541/108857
dc.description.abstractIn order to investigate the importance of 3-methyladenine in cellular sensitivity to chemical methylating agents we have constructed retroviral vectors for the integration and expression of the Escherichia coli tag gene in mammalian cells. The tag gene encodes 3-methyladenine DNA glycosylase-1 which specifically removes 3-alkyladenines from DNA. The constructs were introduced into Chinese hamster V79 cells by liposome mediated transfection or into murine haemopoietic stem cells by cocultivation with a lipofected, virus-packaging cell line. In both cases, stable transfectants were selected for resistance to the antibiotic, G418, conferred by expression of the neo gene carried by the vector. Measurements of 3-methyladenine DNA glycosylase activity in cell extracts showed an up to 10-fold increase in cell lines with stably integrated tag gene sequences. These cell lines were significantly more resistant to the cytotoxic effects of methylmethanesulfonate and N-methyl-N-nitrosourea than their parent cell lines, indicating that 3-methyladenine repair is a limiting factor in cellular resistance to these methylating agents. Furthermore, the mutation frequency induced by methylmethanesulfonate was reduced to 50% of normal by expression of 3-methyladenine I activity in the Chinese hamster cells, indicating that m3A is not only a cytotoxic but also a premutagenic lesion in mammalian cells. It is concluded that an alkylation repair gene function of a type only thought to be present in bacteria can yield a hyperresistant phenotype when transferred to mammalian cells.
dc.language.isoenen
dc.subject.meshAlkylating Agents
dc.subject.meshAnimals
dc.subject.meshBase Sequence
dc.subject.meshCell Line
dc.subject.meshCell Survival
dc.subject.meshCricetinae
dc.subject.meshCricetulus
dc.subject.meshDNA Glycosylases
dc.subject.meshDNA Repair
dc.subject.meshDNA, Single-Stranded
dc.subject.meshDrug Resistance
dc.subject.meshEscherichia coli
dc.subject.meshGenes, Bacterial
dc.subject.meshMethyl Methanesulfonate
dc.subject.meshMethylation
dc.subject.meshMethylnitrosourea
dc.subject.meshMolecular Sequence Data
dc.subject.meshMutagens
dc.subject.meshN-Glycosyl Hydrolases
dc.subject.meshPlasmids
dc.subject.meshTransfection
dc.titleExpression of the E.coli 3-methyladenine DNA glycosylase I gene in mammalian cells reduces the toxic and mutagenic effects of methylating agents.en
dc.typeArticleen
dc.contributor.departmentBiotechnology Centre of Oslo, Blindern, Norway.en
dc.identifier.journalEMBO Journalen
html.description.abstractIn order to investigate the importance of 3-methyladenine in cellular sensitivity to chemical methylating agents we have constructed retroviral vectors for the integration and expression of the Escherichia coli tag gene in mammalian cells. The tag gene encodes 3-methyladenine DNA glycosylase-1 which specifically removes 3-alkyladenines from DNA. The constructs were introduced into Chinese hamster V79 cells by liposome mediated transfection or into murine haemopoietic stem cells by cocultivation with a lipofected, virus-packaging cell line. In both cases, stable transfectants were selected for resistance to the antibiotic, G418, conferred by expression of the neo gene carried by the vector. Measurements of 3-methyladenine DNA glycosylase activity in cell extracts showed an up to 10-fold increase in cell lines with stably integrated tag gene sequences. These cell lines were significantly more resistant to the cytotoxic effects of methylmethanesulfonate and N-methyl-N-nitrosourea than their parent cell lines, indicating that 3-methyladenine repair is a limiting factor in cellular resistance to these methylating agents. Furthermore, the mutation frequency induced by methylmethanesulfonate was reduced to 50% of normal by expression of 3-methyladenine I activity in the Chinese hamster cells, indicating that m3A is not only a cytotoxic but also a premutagenic lesion in mammalian cells. It is concluded that an alkylation repair gene function of a type only thought to be present in bacteria can yield a hyperresistant phenotype when transferred to mammalian cells.


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