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The small RNA RssR regulates myo-inositol degradation by Salmonella enterica
Small noncoding RNAs (sRNAs) with putative regulatory functions in gene expression have been identified in the enteropathogen Salmonella enterica serovar Typhimurium (S. Typhimurium). Two sRNAs are encoded by the genomic island GEI4417/4436 responsible for myo-inositol (MI) degradation, suggesting a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288124/ https://www.ncbi.nlm.nih.gov/pubmed/30531898 http://dx.doi.org/10.1038/s41598-018-35784-8 |
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author | Kröger, Carsten Rothhardt, Johannes E. Brokatzky, Dominik Felsl, Angela Kary, Stefani C. Heermann, Ralf Fuchs, Thilo M. |
author_facet | Kröger, Carsten Rothhardt, Johannes E. Brokatzky, Dominik Felsl, Angela Kary, Stefani C. Heermann, Ralf Fuchs, Thilo M. |
author_sort | Kröger, Carsten |
collection | PubMed |
description | Small noncoding RNAs (sRNAs) with putative regulatory functions in gene expression have been identified in the enteropathogen Salmonella enterica serovar Typhimurium (S. Typhimurium). Two sRNAs are encoded by the genomic island GEI4417/4436 responsible for myo-inositol (MI) degradation, suggesting a role in the regulation of this metabolic pathway. We show that a lack of the sRNA STnc2160, termed RssR, results in a severe growth defect in minimal medium (MM) with MI. In contrast, the second sRNA STnc1740 was induced in the presence of glucose, and its overexpression slightly attenuated growth in the presence of MI. Constitutive expression of RssR led to an increased stability of the reiD mRNA, which encodes an activator of iol genes involved in MI utilization, via interaction with its 5′-UTR. SsrB, a response regulator contributing to the virulence properties of salmonellae, activated rssR transcription by binding the sRNA promoter. In addition, the absence of the RNA chaperone Hfq resulted in strongly decreased levels of RssR, attenuated S. Typhimurium growth with MI, and reduced expression of several iol genes required for MI degradation. Considered together, the extrinsic RssR allows fine regulation of cellular ReiD levels and thus of MI degradation by acting on the reiD mRNA stability. |
format | Online Article Text |
id | pubmed-6288124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62881242018-12-19 The small RNA RssR regulates myo-inositol degradation by Salmonella enterica Kröger, Carsten Rothhardt, Johannes E. Brokatzky, Dominik Felsl, Angela Kary, Stefani C. Heermann, Ralf Fuchs, Thilo M. Sci Rep Article Small noncoding RNAs (sRNAs) with putative regulatory functions in gene expression have been identified in the enteropathogen Salmonella enterica serovar Typhimurium (S. Typhimurium). Two sRNAs are encoded by the genomic island GEI4417/4436 responsible for myo-inositol (MI) degradation, suggesting a role in the regulation of this metabolic pathway. We show that a lack of the sRNA STnc2160, termed RssR, results in a severe growth defect in minimal medium (MM) with MI. In contrast, the second sRNA STnc1740 was induced in the presence of glucose, and its overexpression slightly attenuated growth in the presence of MI. Constitutive expression of RssR led to an increased stability of the reiD mRNA, which encodes an activator of iol genes involved in MI utilization, via interaction with its 5′-UTR. SsrB, a response regulator contributing to the virulence properties of salmonellae, activated rssR transcription by binding the sRNA promoter. In addition, the absence of the RNA chaperone Hfq resulted in strongly decreased levels of RssR, attenuated S. Typhimurium growth with MI, and reduced expression of several iol genes required for MI degradation. Considered together, the extrinsic RssR allows fine regulation of cellular ReiD levels and thus of MI degradation by acting on the reiD mRNA stability. Nature Publishing Group UK 2018-12-10 /pmc/articles/PMC6288124/ /pubmed/30531898 http://dx.doi.org/10.1038/s41598-018-35784-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kröger, Carsten Rothhardt, Johannes E. Brokatzky, Dominik Felsl, Angela Kary, Stefani C. Heermann, Ralf Fuchs, Thilo M. The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title | The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title_full | The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title_fullStr | The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title_full_unstemmed | The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title_short | The small RNA RssR regulates myo-inositol degradation by Salmonella enterica |
title_sort | small rna rssr regulates myo-inositol degradation by salmonella enterica |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288124/ https://www.ncbi.nlm.nih.gov/pubmed/30531898 http://dx.doi.org/10.1038/s41598-018-35784-8 |
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