Literature DB >> 10027977

Regulation of excision of the conjugative transposon Tn916.

D Marra1, J R Scott.   

Abstract

Excision from the donor DNA molecule is the first step in conjugative transposition of Tn916 and is followed by circularization of the transposon and its transfer to a new host. We have demonstrated that, in Gram-positive hosts, the Xis protein, as well as the site-specific recombinase Int, is required for the excision of Tn916. Using assays for closure of the excised covalently closed transposon and for repair of the donor DNA molecule, we found that neither protein alone is rate limiting for excision, but overexpression of Int and Xis together results in increased excision. After excision, the frequency of Tn916 circle formation was found to be the same as the frequency of repair of the donor DNA molecule. This suggests that a single reaction results in the closure of both molecules. We have also identified two transcripts that encode Int, one of which also encodes Xis and one of which does not, suggesting that there are steps in conjugative transposition of Tn916 that require Int without Xis.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10027977     DOI: 10.1046/j.1365-2958.1999.01201.x

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


  21 in total

1.  Specific binding of integrase to the origin of transfer (oriT) of the conjugative transposon Tn916.

Authors:  D Hinerfeld; G Churchward
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

2.  The frequency of conjugative transposition of Tn916 is not determined by the frequency of excision.

Authors:  D Marra; B Pethel; G G Churchward; J R Scott
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

3.  Transfer of TN916-like elements in microcosm dental plaques.

Authors:  A P Roberts; G Cheah; D Ready; J Pratten; M Wilson; P Mullany
Journal:  Antimicrob Agents Chemother       Date:  2001-10       Impact factor: 5.191

4.  Excision of the conjugative transposon Tn916 in Lactococcus lactis.

Authors:  D Marra; J G Smith; J R Scott
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

5.  Characterization of Tn916S, a Tn916-like element containing the tetracycline resistance determinant tet(S).

Authors:  Holli Lancaster; Adam P Roberts; Raman Bedi; Michael Wilson; Peter Mullany
Journal:  J Bacteriol       Date:  2004-07       Impact factor: 3.490

Review 6.  Integrative and conjugative elements: mosaic mobile genetic elements enabling dynamic lateral gene flow.

Authors:  Rachel A F Wozniak; Matthew K Waldor
Journal:  Nat Rev Microbiol       Date:  2010-07-05       Impact factor: 60.633

7.  The integrase of the conjugative transposon Tn916 directs strand- and sequence-specific cleavage of the origin of conjugal transfer, oriT, by the endonuclease Orf20.

Authors:  Jennifer M Rocco; Gordon Churchward
Journal:  J Bacteriol       Date:  2006-03       Impact factor: 3.490

8.  Characterization of the ends and target sites of the novel conjugative transposon Tn5397 from Clostridium difficile: excision and circularization is mediated by the large resolvase, TndX.

Authors:  H Wang; A P Roberts; D Lyras; J I Rood; M Wilks; P Mullany
Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

9.  Autonomous Replication of the Conjugative Transposon Tn916.

Authors:  Laurel D Wright; Alan D Grossman
Journal:  J Bacteriol       Date:  2016-11-18       Impact factor: 3.490

10.  Possible origins of CTnBST, a conjugative transposon found recently in a human colonic Bacteroides strain.

Authors:  David J Schlesinger; Nadja B Shoemaker; Abigail A Salyers
Journal:  Appl Environ Microbiol       Date:  2007-05-04       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.