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Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery

Conjugation is a major mechanism of horizontal gene transfer promoting the spread of antibiotic resistance among human pathogens. It involves establishing a junction between a donor and a recipient cell via an extracellular appendage known as the mating pilus. In bacteria, the conjugation machinery...

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Autores principales: Beltran, Leticia C., Cvirkaite-Krupovic, Virginija, Miller, Jessalyn, Wang, Fengbin, Kreutzberger, Mark A. B., Patkowski, Jonasz B., Costa, Tiago R. D., Schouten, Stefan, Levental, Ilya, Conticello, Vincent P., Egelman, Edward H., Krupovic, Mart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905601/
https://www.ncbi.nlm.nih.gov/pubmed/36750723
http://dx.doi.org/10.1038/s41467-023-36349-8
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author Beltran, Leticia C.
Cvirkaite-Krupovic, Virginija
Miller, Jessalyn
Wang, Fengbin
Kreutzberger, Mark A. B.
Patkowski, Jonasz B.
Costa, Tiago R. D.
Schouten, Stefan
Levental, Ilya
Conticello, Vincent P.
Egelman, Edward H.
Krupovic, Mart
author_facet Beltran, Leticia C.
Cvirkaite-Krupovic, Virginija
Miller, Jessalyn
Wang, Fengbin
Kreutzberger, Mark A. B.
Patkowski, Jonasz B.
Costa, Tiago R. D.
Schouten, Stefan
Levental, Ilya
Conticello, Vincent P.
Egelman, Edward H.
Krupovic, Mart
author_sort Beltran, Leticia C.
collection PubMed
description Conjugation is a major mechanism of horizontal gene transfer promoting the spread of antibiotic resistance among human pathogens. It involves establishing a junction between a donor and a recipient cell via an extracellular appendage known as the mating pilus. In bacteria, the conjugation machinery is encoded by plasmids or transposons and typically mediates the transfer of cognate mobile genetic elements. Much less is known about conjugation in archaea. Here, we determine atomic structures by cryo-electron microscopy of three conjugative pili, two from hyperthermophilic archaea (Aeropyrum pernix and Pyrobaculum calidifontis) and one encoded by the Ti plasmid of the bacterium Agrobacterium tumefaciens, and show that the archaeal pili are homologous to bacterial mating pili. However, the archaeal conjugation machinery, known as Ced, has been ‘domesticated’, that is, the genes for the conjugation machinery are encoded on the chromosome rather than on mobile genetic elements, and mediates the transfer of cellular DNA.
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spelling pubmed-99056012023-02-08 Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery Beltran, Leticia C. Cvirkaite-Krupovic, Virginija Miller, Jessalyn Wang, Fengbin Kreutzberger, Mark A. B. Patkowski, Jonasz B. Costa, Tiago R. D. Schouten, Stefan Levental, Ilya Conticello, Vincent P. Egelman, Edward H. Krupovic, Mart Nat Commun Article Conjugation is a major mechanism of horizontal gene transfer promoting the spread of antibiotic resistance among human pathogens. It involves establishing a junction between a donor and a recipient cell via an extracellular appendage known as the mating pilus. In bacteria, the conjugation machinery is encoded by plasmids or transposons and typically mediates the transfer of cognate mobile genetic elements. Much less is known about conjugation in archaea. Here, we determine atomic structures by cryo-electron microscopy of three conjugative pili, two from hyperthermophilic archaea (Aeropyrum pernix and Pyrobaculum calidifontis) and one encoded by the Ti plasmid of the bacterium Agrobacterium tumefaciens, and show that the archaeal pili are homologous to bacterial mating pili. However, the archaeal conjugation machinery, known as Ced, has been ‘domesticated’, that is, the genes for the conjugation machinery are encoded on the chromosome rather than on mobile genetic elements, and mediates the transfer of cellular DNA. Nature Publishing Group UK 2023-02-07 /pmc/articles/PMC9905601/ /pubmed/36750723 http://dx.doi.org/10.1038/s41467-023-36349-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Beltran, Leticia C.
Cvirkaite-Krupovic, Virginija
Miller, Jessalyn
Wang, Fengbin
Kreutzberger, Mark A. B.
Patkowski, Jonasz B.
Costa, Tiago R. D.
Schouten, Stefan
Levental, Ilya
Conticello, Vincent P.
Egelman, Edward H.
Krupovic, Mart
Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title_full Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title_fullStr Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title_full_unstemmed Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title_short Archaeal DNA-import apparatus is homologous to bacterial conjugation machinery
title_sort archaeal dna-import apparatus is homologous to bacterial conjugation machinery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905601/
https://www.ncbi.nlm.nih.gov/pubmed/36750723
http://dx.doi.org/10.1038/s41467-023-36349-8
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