Literature DB >> 10760133

The role of tandem IS dimers in IS911 transposition.

C Turlan1, B Ton-Hoang, M Chandler.   

Abstract

Using a combined in vivo and in vitro approach, we demonstrated that the transposition products generated by IS911 from a dimeric donor plasmid are different from those generated from a plasmid monomer. When carried by a monomeric plasmid donor, free IS911 transposon circles are generated by intra-IS recombination in which one IS end undergoes attack by the other. These represent transposition intermediates that undergo integration using the abutted left (IRL) and right (IRR) ends of the element, the active IRR-IRL junction, to generate simple insertions. In contrast, the two IS911 copies carried by a dimeric donor plasmid not only underwent intra-IS recombination to generate transposon circles but additionally participated in inter-IS recombination. This also creates an active IRR-IRL junction by generating a head-to-tail IS tandem dimer ([IS]2) in which one of the original plasmid backbone copies is eliminated in the formation of the junction. Both transposon circles and IS tandem dimers are generated from an intermediate in which two transposon ends are retained by a single strand joint to generate a figure 8 molecule. Inter-IS figure 8 molecules generated in vitro could be resolved into the [IS]2 form following introduction into a host strain by transformation. Resolution did not require IS911 transposase. The [IS]2 structure was stable in the absence of transposase but was highly unstable in its presence both in vivo and in vitro. Previous studies had demonstrated that the IRR-IRL junction promotes efficient intermolecular integration and intramolecular deletions both in vivo and in vitro. Integration of the [IS]2 derivative would result in a product that resembles a co-integrate structure. It is also shown here that the IRR-IRL junction of the [IS]2 form and derivative structures can specifically target one of the other ends in an intramolecular transposition reaction to generate transposon circles in vitro. These results not only demonstrate that IS911 (and presumably other members of the IS3 family) is capable of generating a range of transposition products, it also provides a mechanistic framework which explains the formation and activity of such structures previously observed for several other unrelated IS elements. This behaviour is probably characteristic of a large number of IS elements.

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Year:  2000        PMID: 10760133     DOI: 10.1046/j.1365-2958.2000.01800.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  10 in total

1.  Diversity of Tn4001 transposition products: the flanking IS256 elements can form tandem dimers and IS circles.

Authors:  M Prudhomme; C Turlan; J-P Claverys; M Chandler
Journal:  J Bacteriol       Date:  2002-01       Impact factor: 3.490

2.  Escherichia coli insertion sequence IS150: transposition via circular and linear intermediates.

Authors:  Markus Haas; Bodo Rak
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

3.  Site-specific recombination by the DDE family member mobile element IS30 transposase.

Authors:  János Kiss; Mónika Szabó; Ferenc Olasz
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-09       Impact factor: 11.205

4.  Transposase-dependent formation of circular IS256 derivatives in Staphylococcus epidermidis and Staphylococcus aureus.

Authors:  Isabel Loessner; Katja Dietrich; Dorothea Dittrich; Jörg Hacker; Wilma Ziebuhr
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

5.  A target specificity switch in IS911 transposition: the role of the OrfA protein.

Authors:  C Loot; C Turlan; P Rousseau; B Ton-Hoang; M Chandler
Journal:  EMBO J       Date:  2002-08-01       Impact factor: 11.598

6.  Requirement of IS911 replication before integration defines a new bacterial transposition pathway.

Authors:  G Duval-Valentin; B Marty-Cointin; M Chandler
Journal:  EMBO J       Date:  2004-09-09       Impact factor: 11.598

7.  Bias between the left and right inverted repeats during IS911 targeted insertion.

Authors:  P Rousseau; C Loot; C Turlan; S Nolivos; M Chandler
Journal:  J Bacteriol       Date:  2008-06-27       Impact factor: 3.490

8.  Analysis of IS1236-mediated gene amplification events in Acinetobacter baylyi ADP1.

Authors:  Laura E Cuff; Kathryn T Elliott; Sarah C Seaton; Maliha K Ishaq; Nicole S Laniohan; Anna C Karls; Ellen L Neidle
Journal:  J Bacteriol       Date:  2012-06-15       Impact factor: 3.490

9.  IS911 transpososome assembly as analysed by tethered particle motion.

Authors:  N Pouget; C Turlan; N Destainville; L Salomé; M Chandler
Journal:  Nucleic Acids Res       Date:  2006-08-21       Impact factor: 16.971

10.  The dynamic network of IS30 transposition pathways.

Authors:  Ferenc Olasz; Mónika Szabó; Alexandra Veress; Márton Bibó; János Kiss
Journal:  PLoS One       Date:  2022-07-28       Impact factor: 3.752

  10 in total

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