Stimulation of precise excision and recombination by conjugal proficient F′ plasmids

Michael Syvanen, John D. Hopkins, Thomas J. Griffin IV, Tsan Yang Liang, Karin Ippen-Ihler, Richard Kolodner

Research output: Contribution to journalArticle

19 Scopus citations

Abstract

Large F plasmids such as F′128 stimulate precise excision of the transposons Tn 5 and Tn 10 in E. coli K12. This stimulation occurs when the transposons are either on the F′128 plasmid or the bacterial chromosome. Stimulation of precise excision is dependent upon conjugal transfer proficient F′ plasmids. Tra- mutations which are defective in conjugal transfer negate this F′128 plasmid stimulation effect. F′128 traS mutations, which are surface exclusion defective and thus permit matings between male cells, thereby increasing conjugal transfer, increase the F plasmid stimulation effect. When the F′ plasmid is present in a cell with the small plasmid, pRS31, carrying the traS to traZ region of F, stimulation of precise excision is no longer observed. This complementation-like activity by pRS31 is abolished by a Tn 5 insertion in the traS gene. Data are presented supporting the notion that F′ plasmid stimulation of precise excision occurs in the recipient during conjugal transfer. F′128 traS also stimulates recA-dependent recombination between DNA sequences on the small, nontransferrable plasmid pRDK41, DNA sequences that are unrelated to those of the F plasmid. The F′ plasmid stimulation of precise excision of Tn 5 is not seen with F+ but only with certain F's with large insertions of chromosomal DNA.

Original languageEnglish (US)
Pages (from-to)1-7
Number of pages7
JournalMGG Molecular & General Genetics
Volume203
Issue number1
DOIs
StatePublished - Apr 1986
Externally publishedYes

Keywords

  • Precise excision
  • recA
  • Surface exclusion
  • tra mutants
  • Transposon

ASJC Scopus subject areas

  • Genetics

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