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''' | '''Sledziewska-Gójska, E and Janion, C''' (1989) Alternative pathways of methyl methanesulfonate-induced mutagenesis in Escherichia coli. ''Mol. Gen. Genet.'' '''216''':126-31 | ||
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!align=left |Abstract | !align=left |Abstract | ||
Latest revision as of 04:44, 15 September 2013
| Citation |
Sledziewska-Gójska, E and Janion, C (1989) Alternative pathways of methyl methanesulfonate-induced mutagenesis in Escherichia coli. Mol. Gen. Genet. 216:126-31 |
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| Abstract |
Methyl methanesulfonate (MMS) induced mutagenesis is known to be largely dependent on functional umuCD and recA genes. By phenotypic analysis of Arg+ (argE3, ochre) revertants according to their reversion of the mutations his-4 (ochre) and thr-1 (amber), we attempted to deduce the specificity and/or sites of MMS-induced mutations. It is shown that: (1) MMS-induced, umuC-dependent Arg+ revertants (which prevail in bacteria proficient in mismatch repair) result from a different mutational pathway from umuC-independent ones. UmuC-dependent Arg+ revertants belong to class 2 (Arg+His+Thr-), and umuC-independent ones to class 1 (Arg+His-Thr-). (2) The mismatch repair system very efficiently prevents mutations induced by MMS. We found that in the mutS strain, deficient in mismatch repair, class 1 Arg+ revertants are the most numerous, whereas class 2 Arg+ revertants occur at similar levels in MMS-treated mutS and mutS+ strains. Therefore the mismatch repair system very efficiently prevents formation of umuC-independent Arg+ revertants, but exerts negligible or no effect on umuC-dependent Arg+ revertants. (iii) Both mutS umuC and mutS recA strains, are highly mutable by MMS. |
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| Keywords |
Arginine/metabolism; Bacterial Proteins/genetics; DNA Repair; Escherichia coli/drug effects; Escherichia coli/genetics; Escherichia coli/metabolism; Genes, Bacterial; Methyl Methanesulfonate/pharmacology; Mutagens; Mutation; Rec A Recombinases/genetics |
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