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Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors
Competence for genetic transformation in Streptococcus pneumoniae develops in response to accumulation of a secreted peptide pheromone and was one of the initial examples of bacterial quorum sensing. Activation of this signaling system induces not only expression of the proteins required for transfo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175624/ https://www.ncbi.nlm.nih.gov/pubmed/21933920 http://dx.doi.org/10.1128/mBio.00071-11 |
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author | Stevens, Kathleen E. Chang, Diana Zwack, Erin E. Sebert, Michael E. |
author_facet | Stevens, Kathleen E. Chang, Diana Zwack, Erin E. Sebert, Michael E. |
author_sort | Stevens, Kathleen E. |
collection | PubMed |
description | Competence for genetic transformation in Streptococcus pneumoniae develops in response to accumulation of a secreted peptide pheromone and was one of the initial examples of bacterial quorum sensing. Activation of this signaling system induces not only expression of the proteins required for transformation but also the production of cellular chaperones and proteases. We have shown here that activity of this pathway is sensitively responsive to changes in the accuracy of protein synthesis that are triggered by either mutations in ribosomal proteins or exposure to antibiotics. Increasing the error rate during ribosomal decoding promoted competence, while reducing the error rate below the baseline level repressed the development of both spontaneous and antibiotic-induced competence. This pattern of regulation was promoted by the bacterial HtrA serine protease. Analysis of strains with the htrA (S234A) catalytic site mutation showed that the proteolytic activity of HtrA selectively repressed competence when translational fidelity was high but not when accuracy was low. These findings redefine the pneumococcal competence pathway as a response to errors during protein synthesis. This response has the capacity to address the immediate challenge of misfolded proteins through production of chaperones and proteases and may also be able to address, through genetic exchange, upstream coding errors that cause intrinsic protein folding defects. The competence pathway may thereby represent a strategy for dealing with lesions that impair proper protein coding and for maintaining the coding integrity of the genome. |
format | Online Article Text |
id | pubmed-3175624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-31756242011-09-20 Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors Stevens, Kathleen E. Chang, Diana Zwack, Erin E. Sebert, Michael E. mBio Research Article Competence for genetic transformation in Streptococcus pneumoniae develops in response to accumulation of a secreted peptide pheromone and was one of the initial examples of bacterial quorum sensing. Activation of this signaling system induces not only expression of the proteins required for transformation but also the production of cellular chaperones and proteases. We have shown here that activity of this pathway is sensitively responsive to changes in the accuracy of protein synthesis that are triggered by either mutations in ribosomal proteins or exposure to antibiotics. Increasing the error rate during ribosomal decoding promoted competence, while reducing the error rate below the baseline level repressed the development of both spontaneous and antibiotic-induced competence. This pattern of regulation was promoted by the bacterial HtrA serine protease. Analysis of strains with the htrA (S234A) catalytic site mutation showed that the proteolytic activity of HtrA selectively repressed competence when translational fidelity was high but not when accuracy was low. These findings redefine the pneumococcal competence pathway as a response to errors during protein synthesis. This response has the capacity to address the immediate challenge of misfolded proteins through production of chaperones and proteases and may also be able to address, through genetic exchange, upstream coding errors that cause intrinsic protein folding defects. The competence pathway may thereby represent a strategy for dealing with lesions that impair proper protein coding and for maintaining the coding integrity of the genome. American Society of Microbiology 2011-09-20 /pmc/articles/PMC3175624/ /pubmed/21933920 http://dx.doi.org/10.1128/mBio.00071-11 Text en Copyright © 2011 Stevens et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Stevens, Kathleen E. Chang, Diana Zwack, Erin E. Sebert, Michael E. Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title | Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title_full | Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title_fullStr | Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title_full_unstemmed | Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title_short | Competence in Streptococcus pneumoniae Is Regulated by the Rate of Ribosomal Decoding Errors |
title_sort | competence in streptococcus pneumoniae is regulated by the rate of ribosomal decoding errors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175624/ https://www.ncbi.nlm.nih.gov/pubmed/21933920 http://dx.doi.org/10.1128/mBio.00071-11 |
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