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Toxin MqsR cleaves single‐stranded mRNA with various 5' ends

Toxin/antitoxin (TA) systems are the means by which bacterial cells become persistent; that is, those cells that are tolerant to multiple environmental stresses such as antibiotics by becoming metabolically dormant. These persister cells are responsible for recalcitrant infections. Once toxins are a...

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Autores principales: Chowdhury, Nityananda, Kwan, Brian W., McGibbon, Louise C., Babitzke, Paul, Wood, Thomas K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905990/
https://www.ncbi.nlm.nih.gov/pubmed/26846703
http://dx.doi.org/10.1002/mbo3.335
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author Chowdhury, Nityananda
Kwan, Brian W.
McGibbon, Louise C.
Babitzke, Paul
Wood, Thomas K.
author_facet Chowdhury, Nityananda
Kwan, Brian W.
McGibbon, Louise C.
Babitzke, Paul
Wood, Thomas K.
author_sort Chowdhury, Nityananda
collection PubMed
description Toxin/antitoxin (TA) systems are the means by which bacterial cells become persistent; that is, those cells that are tolerant to multiple environmental stresses such as antibiotics by becoming metabolically dormant. These persister cells are responsible for recalcitrant infections. Once toxins are activated by the inactivation of antitoxins (e.g., stress‐triggered Lon degradation of the antitoxin), many toxins reduce metabolism by inhibiting translation (e.g., cleaving mRNA, reducing ATP). The MqsR/MqsA TA system of Escherichia coli cleaves mRNA to help the cell withstand oxidative and bile acid stress. Here, we investigated the role of secondary structure and 5′ mRNA processing on MqsR degradation of mRNA and found that MqsR cleaves only single‐stranded RNA at 5′‐GCU sites and that MqsR is equally active against RNA with 5′‐triphosphate, 5′‐monophosphate, and 5′‐hydroxyl groups.
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spelling pubmed-49059902016-06-15 Toxin MqsR cleaves single‐stranded mRNA with various 5' ends Chowdhury, Nityananda Kwan, Brian W. McGibbon, Louise C. Babitzke, Paul Wood, Thomas K. Microbiologyopen Original Research Toxin/antitoxin (TA) systems are the means by which bacterial cells become persistent; that is, those cells that are tolerant to multiple environmental stresses such as antibiotics by becoming metabolically dormant. These persister cells are responsible for recalcitrant infections. Once toxins are activated by the inactivation of antitoxins (e.g., stress‐triggered Lon degradation of the antitoxin), many toxins reduce metabolism by inhibiting translation (e.g., cleaving mRNA, reducing ATP). The MqsR/MqsA TA system of Escherichia coli cleaves mRNA to help the cell withstand oxidative and bile acid stress. Here, we investigated the role of secondary structure and 5′ mRNA processing on MqsR degradation of mRNA and found that MqsR cleaves only single‐stranded RNA at 5′‐GCU sites and that MqsR is equally active against RNA with 5′‐triphosphate, 5′‐monophosphate, and 5′‐hydroxyl groups. John Wiley and Sons Inc. 2016-02-05 /pmc/articles/PMC4905990/ /pubmed/26846703 http://dx.doi.org/10.1002/mbo3.335 Text en © 2016 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Chowdhury, Nityananda
Kwan, Brian W.
McGibbon, Louise C.
Babitzke, Paul
Wood, Thomas K.
Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title_full Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title_fullStr Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title_full_unstemmed Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title_short Toxin MqsR cleaves single‐stranded mRNA with various 5' ends
title_sort toxin mqsr cleaves single‐stranded mrna with various 5' ends
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905990/
https://www.ncbi.nlm.nih.gov/pubmed/26846703
http://dx.doi.org/10.1002/mbo3.335
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