RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact

The regulation of RNA decay is now widely recognized as having a central role in bacterial adaption to environmental stress. Here we present an overview on the diversity of ribonucleases (RNases) and their impact at the posttranscriptional level in the human pathogen Staphylococcus aureus. RNases in...

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Main Authors: Bonnin, Rémy A., Bouloc, Philippe
Format: Online
Language:English
Published: Hindawi Publishing Corporation 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419217/
id pubmed-4419217
recordtype oai_dc
spelling pubmed-44192172015-05-14 RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact Bonnin, Rémy A. Bouloc, Philippe Review Article The regulation of RNA decay is now widely recognized as having a central role in bacterial adaption to environmental stress. Here we present an overview on the diversity of ribonucleases (RNases) and their impact at the posttranscriptional level in the human pathogen Staphylococcus aureus. RNases in prokaryotes have been mainly studied in the two model organisms Escherichia coli and Bacillus subtilis. Based on identified RNases in these two models, putative orthologs have been identified in S. aureus. The main staphylococcal RNases involved in the processing and degradation of the bulk RNA are (i) endonucleases RNase III and RNase Y and (ii) exonucleases RNase J1/J2 and PNPase, having 5′ to 3′ and 3′ to 5′ activities, respectively. The diversity and potential roles of each RNase and of Hfq and RppH are discussed in the context of recent studies, some of which are based on next-generation sequencing technology. Hindawi Publishing Corporation 2015 2015-04-21 /pmc/articles/PMC4419217/ /pubmed/25977913 http://dx.doi.org/10.1155/2015/395753 Text en Copyright © 2015 R. A. Bonnin and P. Bouloc. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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 Bonnin, Rémy A.
Bouloc, Philippe
spellingShingle Bonnin, Rémy A.
Bouloc, Philippe
RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
author_facet Bonnin, Rémy A.
Bouloc, Philippe
author_sort Bonnin, Rémy A.
title RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
title_short RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
title_full RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
title_fullStr RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
title_full_unstemmed RNA Degradation in Staphylococcus aureus: Diversity of Ribonucleases and Their Impact
title_sort rna degradation in staphylococcus aureus: diversity of ribonucleases and their impact
description The regulation of RNA decay is now widely recognized as having a central role in bacterial adaption to environmental stress. Here we present an overview on the diversity of ribonucleases (RNases) and their impact at the posttranscriptional level in the human pathogen Staphylococcus aureus. RNases in prokaryotes have been mainly studied in the two model organisms Escherichia coli and Bacillus subtilis. Based on identified RNases in these two models, putative orthologs have been identified in S. aureus. The main staphylococcal RNases involved in the processing and degradation of the bulk RNA are (i) endonucleases RNase III and RNase Y and (ii) exonucleases RNase J1/J2 and PNPase, having 5′ to 3′ and 3′ to 5′ activities, respectively. The diversity and potential roles of each RNase and of Hfq and RppH are discussed in the context of recent studies, some of which are based on next-generation sequencing technology.
publisher Hindawi Publishing Corporation
publishDate 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419217/
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