Abstract
A strain of Escherichia coli K-12 that overproduces dam methylase 50-fold was found to be hypermutable, and mutations which resulted in loss of excess methylase activity restored mutation frequencies to wild-type levels. These results are consistent with involvement of this deoxyribonucleic acid methylase in mismatch correction.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Cloning, Molecular
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DNA (Cytosine-5-)-Methyltransferases / metabolism*
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DNA Repair
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DNA, Bacterial / metabolism
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Escherichia coli / enzymology
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Escherichia coli / genetics*
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Methyltransferases / metabolism*
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Mutation*
Substances
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DNA, Bacterial
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Methyltransferases
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DNA (Cytosine-5-)-Methyltransferases