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Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila

Natural transformation is the process by which bacteria can actively take up and integrate exogenous DNA thereby providing a source of genetic diversity. Under specific growth conditions the coordinated expression of several genes – a situation referred to as “competence” – allows bacteria to assemb...

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Autores principales: Juan, Pierre-Alexandre, Attaiech, Laetitia, Charpentier, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630621/
https://www.ncbi.nlm.nih.gov/pubmed/26526572
http://dx.doi.org/10.1038/srep16033
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author Juan, Pierre-Alexandre
Attaiech, Laetitia
Charpentier, Xavier
author_facet Juan, Pierre-Alexandre
Attaiech, Laetitia
Charpentier, Xavier
author_sort Juan, Pierre-Alexandre
collection PubMed
description Natural transformation is the process by which bacteria can actively take up and integrate exogenous DNA thereby providing a source of genetic diversity. Under specific growth conditions the coordinated expression of several genes – a situation referred to as “competence” – allows bacteria to assemble a highly processive and dedicated system that can import high molecular weight DNA. Within the cell these large imported DNA molecules are protected from degradation and brought to the chromosome for recombination. Here, we report elevated expression of mreB during competence in the Gram-negative pathogen Legionella pneumophila. Interestingly a similar observation had previously been reported in the distantly-related Gram-positive organism Bacillus subtilis. MreB is often viewed as the bacterial actin homolog contributing to bacterial morphogenesis by coordinating peptidoglycan-synthesising complexes. In addition MreB is increasingly found to be involved in a growing number of processes including chromosome segregation and motor-driven motility. Using genetic and pharmacological approaches, we examined the possible role of MreB during natural transformation in L. pneumophila. Our data show that natural transformation does not require MreB dynamics and exclude a direct role of MreB filaments in the transport of foreign DNA and its recombination in the chromosome.
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spelling pubmed-46306212015-11-05 Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila Juan, Pierre-Alexandre Attaiech, Laetitia Charpentier, Xavier Sci Rep Article Natural transformation is the process by which bacteria can actively take up and integrate exogenous DNA thereby providing a source of genetic diversity. Under specific growth conditions the coordinated expression of several genes – a situation referred to as “competence” – allows bacteria to assemble a highly processive and dedicated system that can import high molecular weight DNA. Within the cell these large imported DNA molecules are protected from degradation and brought to the chromosome for recombination. Here, we report elevated expression of mreB during competence in the Gram-negative pathogen Legionella pneumophila. Interestingly a similar observation had previously been reported in the distantly-related Gram-positive organism Bacillus subtilis. MreB is often viewed as the bacterial actin homolog contributing to bacterial morphogenesis by coordinating peptidoglycan-synthesising complexes. In addition MreB is increasingly found to be involved in a growing number of processes including chromosome segregation and motor-driven motility. Using genetic and pharmacological approaches, we examined the possible role of MreB during natural transformation in L. pneumophila. Our data show that natural transformation does not require MreB dynamics and exclude a direct role of MreB filaments in the transport of foreign DNA and its recombination in the chromosome. Nature Publishing Group 2015-11-03 /pmc/articles/PMC4630621/ /pubmed/26526572 http://dx.doi.org/10.1038/srep16033 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Juan, Pierre-Alexandre
Attaiech, Laetitia
Charpentier, Xavier
Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title_full Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title_fullStr Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title_full_unstemmed Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title_short Natural transformation occurs independently of the essential actin-like MreB cytoskeleton in Legionella pneumophila
title_sort natural transformation occurs independently of the essential actin-like mreb cytoskeleton in legionella pneumophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630621/
https://www.ncbi.nlm.nih.gov/pubmed/26526572
http://dx.doi.org/10.1038/srep16033
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