Type I restriction enzyme with RecA protein promotes illegitimate recombination

Plasmid. 2003 Nov;50(3):202-12. doi: 10.1016/j.plasmid.2003.07.001.

Abstract

Illegitimate (non-homologous) recombination requires little or no sequence homology between recombining DNAs and has been regarded as being a process distinct from homologous recombination, which requires a long stretch of homology between recombining DNAs. However, we have found a type of illegitimate recombination that requires an interaction between long homologous DNA sequences. It was detected when a plasmid that carried 2-kb-long inverted repeats was subjected to type I (EcoKI) restriction in vivo within a special mutant strain of Escherichia coli. In the present work, we analyzed genetic requirements for this type of illegitimate recombination in well-defined genetic backgrounds. Our analysis demonstrated dependence on RecA function and on the presence of two EcoKI sites on the substrate DNA. These results are in harmony with a model in which EcoKI restriction enzyme attacks an intermediate of homologous recombination to divert it to illegitimate recombination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Restriction Enzymes / genetics
  • DNA Restriction Enzymes / metabolism*
  • Deoxyribonucleases, Type I Site-Specific / genetics
  • Deoxyribonucleases, Type I Site-Specific / metabolism
  • Escherichia coli / genetics
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Models, Genetic
  • Molecular Sequence Data
  • Plasmids / genetics
  • Rec A Recombinases / genetics
  • Rec A Recombinases / metabolism*
  • Recombination, Genetic*
  • Repetitive Sequences, Nucleic Acid
  • Sequence Homology, Nucleic Acid

Substances

  • Escherichia coli Proteins
  • Rec A Recombinases
  • DNA Restriction Enzymes
  • endodeoxyribonuclease EcoKI
  • Deoxyribonucleases, Type I Site-Specific