Regulation of the capacity for O6-methylguanine removal from DNA in human lymphoblastoid cells studied by cell hybridization.

Author:

Ayres K,Sklar R,Larson K,Lindgren V,Strauss B

Abstract

Hybrids were made between a ouabain-resistant, thioguanine-resistant human lymphoma line able to remove O6-methylguanine from its DNA (Mex+) and human lymphoblastoid lines deficient in this capability (Mex-). The formation of hybrids was confirmed by chromosomal analysis. Hybrid cells had an O6-methylguanine removal capacity per mole of guanine about one third to one half that of the Mex+ parents, i.e., about the same per cell. Cell hybrids removed the same amount of the alkylation adduct 3-methyladenine as did their parents per mole of guanine, i.e., about twice as much per cell. Although the cell hybrids had intermediate resistance to the cytotoxic action of N-methyl-N'-nitro-N-nitrosoguanidine used to induce O6-methylguanine and 3-methyladenine, there is evidence that the ability to remove O6-methylguanine and resistance to the cytotoxic effect of N-methyl-N'-nitro-N-nitrosoguanidine are dissociable characteristics.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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1. Reversal of Alkylation Damage in DNA;DNA Repair and Mutagenesis;2014-04-30

2. Regulation of Repair of Alkylation Damage in Mammalian Genomes;Progress in Nucleic Acid Research and Molecular Biology;1993

3. The control of O6-methylguanine-DNA methyltransferase (MGMT) activity in mammalian cells: A pre-molecular view;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1990-11

4. Isolation and structural characterization of a cDNA clone encoding the human DNA repair protein for O6-alkylguanine.;Proceedings of the National Academy of Sciences;1990-01-01

5. N-methyl-N-nitrosourea-lnduced mutations in a shuttle plasmid replicated in human cells;Molecular Carcinogenesis;1990

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