Cargando…
Global analysis of mRNA stability in Mycobacterium tuberculosis
Mycobacterium tuberculosis (MTB) is a highly successful pathogen that infects over a billion people. As with most organisms, MTB adapts to stress by modifying its transcriptional profile. Remodeling of the transcriptome requires both altering the transcription rate and clearing away the existing mRN...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592478/ https://www.ncbi.nlm.nih.gov/pubmed/23125364 http://dx.doi.org/10.1093/nar/gks1019 |
_version_ | 1782262125515767808 |
---|---|
author | Rustad, Tige R. Minch, Kyle J. Brabant, William Winkler, Jessica K. Reiss, David J. Baliga, Nitin S. Sherman, David R. |
author_facet | Rustad, Tige R. Minch, Kyle J. Brabant, William Winkler, Jessica K. Reiss, David J. Baliga, Nitin S. Sherman, David R. |
author_sort | Rustad, Tige R. |
collection | PubMed |
description | Mycobacterium tuberculosis (MTB) is a highly successful pathogen that infects over a billion people. As with most organisms, MTB adapts to stress by modifying its transcriptional profile. Remodeling of the transcriptome requires both altering the transcription rate and clearing away the existing mRNA through degradation, a process that can be directly regulated in response to stress. To understand better how MTB adapts to the harsh environs of the human host, we performed a global survey of the decay rates of MTB mRNA transcripts. Decay rates were measured for 2139 of the ∼4000 MTB genes, which displayed an average half-life of 9.5 min. This is nearly twice the average mRNA half-life of other prokaryotic organisms where these measurements have been made. The transcriptome was further stabilized in response to lowered temperature and hypoxic stress. The generally stable transcriptome described here, and the additional stabilization in response to physiologically relevant stresses, has far-ranging implications for how this pathogen is able to adapt in its human host. |
format | Online Article Text |
id | pubmed-3592478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35924782013-03-08 Global analysis of mRNA stability in Mycobacterium tuberculosis Rustad, Tige R. Minch, Kyle J. Brabant, William Winkler, Jessica K. Reiss, David J. Baliga, Nitin S. Sherman, David R. Nucleic Acids Res RNA Mycobacterium tuberculosis (MTB) is a highly successful pathogen that infects over a billion people. As with most organisms, MTB adapts to stress by modifying its transcriptional profile. Remodeling of the transcriptome requires both altering the transcription rate and clearing away the existing mRNA through degradation, a process that can be directly regulated in response to stress. To understand better how MTB adapts to the harsh environs of the human host, we performed a global survey of the decay rates of MTB mRNA transcripts. Decay rates were measured for 2139 of the ∼4000 MTB genes, which displayed an average half-life of 9.5 min. This is nearly twice the average mRNA half-life of other prokaryotic organisms where these measurements have been made. The transcriptome was further stabilized in response to lowered temperature and hypoxic stress. The generally stable transcriptome described here, and the additional stabilization in response to physiologically relevant stresses, has far-ranging implications for how this pathogen is able to adapt in its human host. Oxford University Press 2013-01 2012-11-02 /pmc/articles/PMC3592478/ /pubmed/23125364 http://dx.doi.org/10.1093/nar/gks1019 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | RNA Rustad, Tige R. Minch, Kyle J. Brabant, William Winkler, Jessica K. Reiss, David J. Baliga, Nitin S. Sherman, David R. Global analysis of mRNA stability in Mycobacterium tuberculosis |
title | Global analysis of mRNA stability in Mycobacterium tuberculosis |
title_full | Global analysis of mRNA stability in Mycobacterium tuberculosis |
title_fullStr | Global analysis of mRNA stability in Mycobacterium tuberculosis |
title_full_unstemmed | Global analysis of mRNA stability in Mycobacterium tuberculosis |
title_short | Global analysis of mRNA stability in Mycobacterium tuberculosis |
title_sort | global analysis of mrna stability in mycobacterium tuberculosis |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592478/ https://www.ncbi.nlm.nih.gov/pubmed/23125364 http://dx.doi.org/10.1093/nar/gks1019 |
work_keys_str_mv | AT rustadtiger globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT minchkylej globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT brabantwilliam globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT winklerjessicak globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT reissdavidj globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT baliganitins globalanalysisofmrnastabilityinmycobacteriumtuberculosis AT shermandavidr globalanalysisofmrnastabilityinmycobacteriumtuberculosis |