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PMID: 1986273 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Roles of two types of O6-methylguanine-DNA methyltransferases in DNA repair.

Mutation research ·Vol. 254 ·No. 1 ·1991-01-00 ·Pages 37-44

Takano K, Nakamura T, Sekiguchi M

Abstract

Escherichia coli possesses 2 types of O6-methylguanine-DNA methyltransferases, one inducible and the other constitutive. These enzymes are coded by the ada and the ogt genes, respectively. Using a synthetic ogt-specific probe, we mapped ogt at 29.4 min, near the 5'-flanking region of the nirR gene, on the E. coli chromosome. To elucidate the roles of the 2 types of methyltransferases in DNA repair, we constructed mutant strains which lack either one or both of the genes. In either the ada+ or the ada- background, the ogt mutation had no effect on cell survival after N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) treatment. On the other hand, ada- ogt- cells were more prone to mutation as compared to the ada- ogt+ cells exposed to MNNG. The frequency of spontaneous mutation of cells defective in either one or both of the genes was the same, however, the introduction of the ogt+ plasmid into the cells produced a 2-3-fold decrease in the frequency of spontaneous mutation. O6-Methylguanine-DNA methyltransferases appear to eliminate premutagenic DNA lesions not only from cells exposed to alkylating agents but also from those grown in the absence of the agents.

Related Genes
MeSH Terms
Base Sequence Blotting, Southern Chromosome Mapping Chromosomes, Bacterial Cloning, Molecular DNA Repair Escherichia coli/enzymology,genetics,growth & development Genes, Bacterial Methylnitronitrosoguanidine/pharmacology Methyltransferases/metabolism Molecular Sequence Data Mutation O(6)-Methylguanine-DNA Methyltransferase Oligonucleotide Probes Plasmids Restriction Mapping
Chemicals
Oligonucleotide Probes Methylnitronitrosoguanidine Methyltransferases O(6)-Methylguanine-DNA Methyltransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Takano K
Department of Biochemistry, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Nakamura T
Sekiguchi M
Article Info
Journal
Mutation research
Abbr.
Mutat Res
ISSN
0027-5107
Published
1991-01-00
Pages
37-44
Language
English
Region
Netherlands
NLM ID
0400763
Subset
IM
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