TnpI recombinase: identification of sites within Tn5401 required for TnpI binding and site-specific recombination

Author:

Baum J A1

Affiliation:

1. Ecogen Inc., Langhorne, Pennsylvania 19047-3023, USA.

Abstract

The Bacillus thuringiensis class II transposon Tn5401 encodes a recombinase protein, TnpI, that mediates the resolution of cointegrate molecules generated as intermediates during Tn5401 transposition by the TnpA transposase. This recombination event requires a specific target site, or internal resolution site, at which TnpI binds and catalyzes the exchange of DNA strands. Gel mobility shift assays and DNase I footprinting analyses were used to localize the TnpI binding region to the sequence extending from nucleotides 637 to 747 of Tn5401. Deletions within this region blocked TnpI-mediated recombination in vivo. The 12-bp sequence ATGTCC RCTAAY, present in four copies within the TnpI binding region, is proposed to be the recognition sequence for TnpI binding. TnpI also binds to a single copy of this sequence located within the 53-bp terminal inverted repeats of Tn5401. The unique juxtaposition of recombinase and transposase binding sites at the terminal inverted repeats of Tn5401 suggests that TnpI regulates the binding and/or catalytic activity of TnpA transposase.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference23 articles.

1. Studies on the properties of P1 site-specific recombination: evidence for topologically unlinked products following recombination;Abremski K.;Cell,1983

2. The integrase family of site-specific recombinases: regional similarities and global diversity;Argos P.;EMBO J.,1986

3. Tn5401, a new class II transposable element from Bacillus thuringiensis;Baum J. A.;J. Bacteriol.,1994

4. Baum J. A. Unpublished data.

5. Expression of qa-1F activator protein: identification of upstream binding sites in the qa gene cluster and localization of the DNA-binding domain;Baum J. A.;Mol. Cell. Biol.,1987

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