Abstract
We have cloned a Bacillus subtilis DNA fragment that could correct the defect in a constitutive O6-methylguanine-DNA alkyltransferase (Dat1). This fragment also corrected the hypersensitivity of the strain TKJ6951(ada-1 dat-1) to N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). In the fragment, the gene activity resides in a region of about 850 bp which contains an open reading frame capable of coding for a protein of 165 amino acid residues. The amino acid sequence of this protein exhibits striking similarity to those of E. coli O6-methylguanine-DNA alkyltransferases (Ogt and Ada proteins). We conclude that this is a structural gene for the Dat1 protein, which is distinct from inducible DNA alkyltransferases involved in the adaptive response. The dat-1 mutation was shown to be caused by a structural rearrangement affecting the coding region, and the 0.8 kb transcripts of this gene were detected in dat+ cells but not in dat mutant cells.
MeSH Terms
Bacillus subtilis/drug effects,enzymology,genetics
Base Sequence
Chloramphenicol Resistance/drug effects
Cloning, Molecular
Drug Resistance, Microbial/genetics
Escherichia coli/enzymology,genetics
Genes
Genes, Bacterial
Kinetics
Methylnitronitrosoguanidine/pharmacology
Methyltransferases/genetics,metabolism
Molecular Sequence Data
O(6)-Methylguanine-DNA Methyltransferase
Recombinant Proteins/metabolism
Sequence Homology, Nucleic Acid
Chemicals
Recombinant Proteins
Methylnitronitrosoguanidine
Methyltransferases
O(6)-Methylguanine-DNA Methyltransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Morohoshi F
Radiobiology Division, National Cancer Center Research Institute, Tokyo, Japan.
Hayashi K
Munakata N
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