Interaction of the Gifsy-1 Xis protein with the Gifsy-1 attP sequence

Asa Flanigan, Jeffrey F. Gardner

Research output: Contribution to journalArticlepeer-review

Abstract

The Gifsy-1 phage integrates site specifically into the Salmonella chromosome via an integrase-mediated site-specific recombination mechanism. Initial genetic analysis suggests that Gifsy-1 integrase-mediated excision of the Gifsy-1 phage is influenced by proteins encoded by both the Gifsy-1 and the Gifsy-2 phages. Our studies show that the Gifsy-1 Xis protein regulates the directionality of integrase-mediated excision of the Gifsy-1 phage. Electrophoretic mobility shift assays, DNase I footprinting, dimethyl sulfate (DMS) interference assays, and DMS protection assays were used to identify a 31-base-pair sequence in the attP region to which the Gifsy-1 protein binds. The results suggest that this recombination directionality factor binds in vitro to three imperfect direct repeats, spaced 10 base pairs apart, in a sequential and cooperative manner in the absence of other phage-encoded proteins. Our studies suggest that, while the Gifsy-1 Xis does not require additional factors for specific and high-affinity binding, it may form a microfilament on DNA similar to that described for the phage lambda Xis protein.

Original languageEnglish (US)
Pages (from-to)6303-6311
Number of pages9
JournalJournal of bacteriology
Volume189
Issue number17
DOIs
StatePublished - Sep 2007

ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology

Fingerprint

Dive into the research topics of 'Interaction of the Gifsy-1 Xis protein with the Gifsy-1 attP sequence'. Together they form a unique fingerprint.

Cite this