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...

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Main Authors: Rustad, Tige R., Minch, Kyle J., Brabant, William, Winkler, Jessica K., Reiss, David J., Baliga, Nitin S., Sherman, David R.
Format: Online
Language:English
Published: Oxford University Press 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592478/
id pubmed-3592478
recordtype oai_dc
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. 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.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Rustad, Tige R.
Minch, Kyle J.
Brabant, William
Winkler, Jessica K.
Reiss, David J.
Baliga, Nitin S.
Sherman, David R.
spellingShingle 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
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.
title Global analysis of mRNA stability in Mycobacterium tuberculosis
title_short 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_sort global analysis of mrna stability in mycobacterium tuberculosis
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.
publisher Oxford University Press
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592478/
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