Methyl-directed DNA mismatch repair in Escherichia coli

Mutat Res. 1988 Mar;198(1):37-43. doi: 10.1016/0027-5107(88)90037-1.

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 Analysis of mismatch correction in a defined system (Lahue et al., unpublished) should provide a direct means to further molecular aspects of this process.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

  • Adenine / analogs & derivatives*
  • Adenine / physiology
  • Bacterial Proteins / physiology
  • Base Composition*
  • DNA Ligases / physiology
  • DNA Repair*
  • DNA, Bacterial / genetics
  • DNA, Bacterial / metabolism*
  • DNA-Binding Proteins / physiology
  • Endodeoxyribonucleases / physiology
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Methylation
  • Methyltransferases / physiology
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • DNA-Binding Proteins
  • Methyltransferases
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)
  • Endodeoxyribonucleases
  • DNA Ligases
  • Adenine
  • 6-methyladenine