Abstract
Some of the molecular aspects of methyl-directed mismatch repair in E. coli have been characterized. These include: mismatch recognition by mutS protein in which different mispairs are bound with different affinities; the direct involvement of d(GATC) sites; and strand scission by mutH protein at d(GATC) sequences with strand selection based on methylation of the DNA at those sites. In addition, communication over a distance between a mismatch and d(GATC) sites has been implicated. Analysis of mismatch correction in a defined system (Lahue et al., unpublished) should provide a direct means to further molecular aspects of this process.
MeSH terms
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Adenine / analogs & derivatives*
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Adenine / physiology
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Bacterial Proteins / physiology
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Base Composition*
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DNA Ligases / physiology
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DNA Repair*
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DNA, Bacterial / genetics
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DNA, Bacterial / metabolism*
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DNA-Binding Proteins / physiology
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Endodeoxyribonucleases / physiology
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Escherichia coli / genetics
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Escherichia coli / metabolism*
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Methylation
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Methyltransferases / physiology
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Site-Specific DNA-Methyltransferase (Adenine-Specific)
Substances
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Bacterial Proteins
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DNA, Bacterial
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DNA-Binding Proteins
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Methyltransferases
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Site-Specific DNA-Methyltransferase (Adenine-Specific)
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Endodeoxyribonucleases
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DNA Ligases
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Adenine
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6-methyladenine