Literature DB >> 8407835

Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element.

N B Shoemaker1, G R Wang, A M Stevens, A A Salyers.   

Abstract

The Bacteroides species harbor a family of conjugative transposons called tetracycline resistance elements (Tcr elements) that transfer themselves from the chromosome of a donor to the chromosome of a recipient, mobilize coresident plasmids, and also mediate the excision and circularization of members of a family of 10- to 12-kbp insertion elements which share a small region of DNA homology and are called NBUs (for nonreplicating Bacteroides units). The NBUs are sometimes cotransferred with Tcr elements, and it was postulated previously that the excised circular forms of the NBUs were plasmidlike forms and were transferred like plasmids and then integrated into the recipient chromosome. We used chimeric plasmids containing one of the NBUs, NBU1, and a Bacteroides-Escherichia coli shuttle vector to show that this hypothesis is probably correct. NBU1 contained a region that allowed mobilization by both the Tcr elements and IncP plasmids, and we used these conjugal elements to allow us to estimate the frequencies of excision, mobilization, and integration of NBU1 in Bacteroides hosts to be approximately 10(-2), 10(-5) to 10(-4), and 10(-2), respectively. Although functions on the Tcr elements were required for the excision-circularization and mobilization of NBU1, no Tcr element functions were required for integration into the recipient chromosome. Analysis of the DNA sequences at the integration region of the circular form of NBU1, the primary insertion site in the Bacteroides thetaiotaomicron 5482 chromosome, and the resultant NBU1-chromosome junctions showed that NBU1 appeared to integrate into the primary insertion site by recombining within an identical 14-bp sequence present on both NBU1 and the target, thus leaving a copy of the 14-bp sequence at both junctions. The apparent integration mechanism and the target selection of NBU1 were different from those of both XBU4422, the only member of the conjugal Tcr elements for which these sequences are known, and Tn4399, a mobilizable Bacteroides transposon. The NBUs appear to be a distinct type of mobilizable insertion element.

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Year:  1993        PMID: 8407835      PMCID: PMC206769          DOI: 10.1128/jb.175.20.6578-6587.1993

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  13 in total

1.  PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT.

Authors:  H SAITO; K I MIURA
Journal:  Biochim Biophys Acta       Date:  1963-08-20

2.  Insertion and excision of Bacteroides conjugative chromosomal elements.

Authors:  L A Bedzyk; N B Shoemaker; K E Young; A A Salyers
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

3.  A complementation analysis of the restriction and modification of DNA in Escherichia coli.

Authors:  H W Boyer; D Roulland-Dussoix
Journal:  J Mol Biol       Date:  1969-05-14       Impact factor: 5.469

4.  Mobilization of Bacteroides plasmids by Bacteroides conjugal elements.

Authors:  P J Valentine; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1988-03       Impact factor: 3.490

5.  Facilitated transfer of IncP beta R751 derivatives from the chromosome of Bacteroides uniformis to Escherichia coli recipients by a conjugative Bacteroides tetracycline resistance element.

Authors:  N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1987-07       Impact factor: 3.490

6.  A cryptic 65-kilobase-pair transposonlike element isolated from Bacteroides uniformis has homology with Bacteroides conjugal tetracycline resistance elements.

Authors:  N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1990-04       Impact factor: 3.490

7.  The region of a Bacteroides conjugal chromosomal tetracycline resistance element which is responsible for production of plasmidlike forms from unlinked chromosomal DNA might also be involved in transfer of the element.

Authors:  A M Stevens; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1990-08       Impact factor: 3.490

8.  Tn4399, a conjugal mobilizing transposon of Bacteroides fragilis.

Authors:  D W Hecht; M H Malamy
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

9.  Regions in Bacteroides plasmids pBFTM10 and pB8-51 that allow Escherichia coli-Bacteroides shuttle vectors to be mobilized by IncP plasmids and by a conjugative Bacteroides tetracycline resistance element.

Authors:  N B Shoemaker; C Getty; E P Guthrie; A A Salyers
Journal:  J Bacteriol       Date:  1986-06       Impact factor: 3.490

10.  Tetracycline-dependent appearance of plasmidlike forms in Bacteroides uniformis 0061 mediated by conjugal Bacteroides tetracycline resistance elements.

Authors:  N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

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  32 in total

1.  Characterization of the 13-kilobase ermF region of the Bacteroides conjugative transposon CTnDOT.

Authors:  G Whittle; B D Hund; N B Shoemaker; A A Salyers
Journal:  Appl Environ Microbiol       Date:  2001-08       Impact factor: 4.792

2.  Production of two proteins encoded by the Bacteroides mobilizable transposon NBU1 correlates with time-dependent accumulation of the excised NBu1 circular form.

Authors:  J Wang; G R Wang; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  2001-11       Impact factor: 3.490

3.  Characterization of genes involved in modulation of conjugal transfer of the Bacteroides conjugative transposon CTnDOT.

Authors:  Gabrielle Whittle; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2002-07       Impact factor: 3.490

4.  A bacteroides conjugative transposon, CTnERL, can transfer a portion of itself by conjugation without excising from the chromosome.

Authors:  Gabrielle Whittle; Nathan Hamburger; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

5.  NBU1, a mobilizable site-specific integrated element from Bacteroides spp., can integrate nonspecifically in Escherichia coli.

Authors:  N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

6.  The Bacteroides mobilizable insertion element, NBU1, integrates into the 3' end of a Leu-tRNA gene and has an integrase that is a member of the lambda integrase family.

Authors:  N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

7.  An unexpected effect of tetracycline concentration: growth phase-associated excision of the Bacteroides mobilizable transposon NBU1.

Authors:  Bo Song; Gui-Rong Wang; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2008-10-24       Impact factor: 3.490

8.  Characterization of a new type of Bacteroides conjugative transposon, Tcr Emr 7853.

Authors:  M P Nikolich; N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

9.  Interactions of NBU1 IntN1 and Orf2x proteins with attachment site DNA.

Authors:  Margaret M Wood; Lara Rajeev; Jeffrey F Gardner
Journal:  J Bacteriol       Date:  2013-10-04       Impact factor: 3.490

10.  Identification of a new ribosomal protection type of tetracycline resistance gene, tet(36), from swine manure pits.

Authors:  Gabrielle Whittle; Terence R Whitehead; Nathan Hamburger; Nadja B Shoemaker; Michael A Cotta; Abigail A Salyers
Journal:  Appl Environ Microbiol       Date:  2003-07       Impact factor: 4.792

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