Integration specificity of an artificial kanamycin transposon constructed by the in vitro insertion of an internal Tn5 fragment into IS2

Mol Gen Genet. 1981;183(1):45-50. doi: 10.1007/BF00270136.

Abstract

IS2 has been marked genetically by the in vitro insertion into its HindIII site of a 3.3 Kb HindIII fragment of Tn5 conferring resistance to kanamycin. The transposition of the IS2::Km, thus obtained, to lambda has been found and insertion sites were characterised. Each of ten independent IS2::Km insertions were found at the same site at 61.2% of the lambda map, always in the same orientation (orientation II relative to the xis gene). The integration sites of IS2::Km in five of the kanamycin-transducing phages were determined by DNA sequence analysis, and were found to be identical at the nucleotide level. Further transposition of IS2::Km from lambda to the bacterial chromosome was demonstrated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriophage lambda / genetics
  • Base Sequence
  • DNA Transposable Elements*
  • DNA, Bacterial / analysis
  • DNA, Viral / analysis
  • Drug Resistance, Microbial
  • Electrophoresis, Agar Gel
  • Escherichia coli / genetics*
  • Genes*
  • Genetic Markers*
  • Kanamycin / pharmacology*
  • Recombination, Genetic*

Substances

  • DNA Transposable Elements
  • DNA, Bacterial
  • DNA, Viral
  • Genetic Markers
  • Kanamycin