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Delineation of the integrase-attachment and origin-of-transfer regions of the symbiosis island ICEMlSymR7A.
Verdonk, Callum J; Sullivan, John T; Williman, Kate M; Nicholson, Leila; Bastholm, Tahlia R; Hynes, Michael F; Ronson, Clive W; Bond, Charles S; Ramsay, Joshua P.
Afiliação
  • Verdonk CJ; School of Molecular Sciences, University of Western Australia, Perth, WA, Australia; School of Pharmacy and Biomedical Sciences and Curtin Health Innovation Research Institute, Curtin University, Perth, WA, Australia.
  • Sullivan JT; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
  • Williman KM; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
  • Nicholson L; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
  • Bastholm TR; School of Pharmacy and Biomedical Sciences and Curtin Health Innovation Research Institute, Curtin University, Perth, WA, Australia.
  • Hynes MF; Department of Biological Sciences, University of Calgary, Calgary, Canada.
  • Ronson CW; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
  • Bond CS; School of Molecular Sciences, University of Western Australia, Perth, WA, Australia.
  • Ramsay JP; School of Pharmacy and Biomedical Sciences and Curtin Health Innovation Research Institute, Curtin University, Perth, WA, Australia. Electronic address: josh.ramsay@curtin.edu.au.
Plasmid ; 104: 102416, 2019 07.
Article em En | MEDLINE | ID: mdl-31078551
ABSTRACT
Integrative and conjugative elements (ICEs) are chromosomally-integrated mobile genetic elements that excise from their host chromosome and transfer to other bacteria via conjugation. ICEMlSymR7A is the prototypical member of a large family of "symbiosis ICEs" which confer upon their hosts the ability to form a nitrogen-fixing symbiosis with a variety of legume species. Mesorhizobial symbiosis ICEs carry a common core of mobilisation genes required for integration, excision and conjugative transfer. IntS of ICEMlSymR7A enables recombination between the ICEMlSymR7A attachment site attP and the 3' end of the phe-tRNA gene. Here we identified putative IntS attP arm (P) sites within the attP region and demonstrated that the outermost P1 and P5 sites demarcated the minimal region for efficient IntS-mediated integration. We also identified the ICEMlSymR7A origin-of-transfer (oriT) site directly upstream of the relaxase-gene rlxS. The ICEMlSymR7A conjugation system mobilised a plasmid carrying the cloned oriT to Escherichia coli in an rlxS-dependent manner. Surprisingly, an in-frame, markerless deletion mutation in the ICEMlSymR7A recombination directionality factor (excisionase) gene rdfS, but not a mutation in intS, abolished mobilisation, suggesting the rdfS deletion tentatively has downstream effects on conjugation or its regulation. In summary, this work defines two critical cis-acting regions required for excision and transfer of ICEMlSymR7A and related ICEs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de DNA Transponíveis / Origem de Replicação / Conjugação Genética / Integrases / Ilhas Genômicas Tipo de estudo: Prognostic_studies Idioma: En Revista: Plasmid Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de DNA Transponíveis / Origem de Replicação / Conjugação Genética / Integrases / Ilhas Genômicas Tipo de estudo: Prognostic_studies Idioma: En Revista: Plasmid Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália