Cargando…
A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron
Bacteria of the genus Bacteroides are common members of the human intestinal microbiota and important degraders of polysaccharides in the gut. Among them, the species Bacteroides thetaiotaomicron has emerged as the model organism for functional microbiota research. Here, we use differential RNA sequ...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366714/ https://www.ncbi.nlm.nih.gov/pubmed/32678091 http://dx.doi.org/10.1038/s41467-020-17348-5 |
_version_ | 1783560278603988992 |
---|---|
author | Ryan, Daniel Jenniches, Laura Reichardt, Sarah Barquist, Lars Westermann, Alexander J. |
author_facet | Ryan, Daniel Jenniches, Laura Reichardt, Sarah Barquist, Lars Westermann, Alexander J. |
author_sort | Ryan, Daniel |
collection | PubMed |
description | Bacteria of the genus Bacteroides are common members of the human intestinal microbiota and important degraders of polysaccharides in the gut. Among them, the species Bacteroides thetaiotaomicron has emerged as the model organism for functional microbiota research. Here, we use differential RNA sequencing (dRNA-seq) to generate a single-nucleotide resolution transcriptome map of B. thetaiotaomicron grown under defined laboratory conditions. An online browser, called ‘Theta-Base’ (www.helmholtz-hiri.de/en/datasets/bacteroides), is launched to interrogate the obtained gene expression data and annotations of ~4500 transcription start sites, untranslated regions, operon structures, and 269 noncoding RNA elements. Among the latter is GibS, a conserved, 145 nt-long small RNA that is highly expressed in the presence of N-acetyl-D-glucosamine as sole carbon source. We use computational predictions and experimental data to determine the secondary structure of GibS and identify its target genes. Our results indicate that sensing of N-acetyl-D-glucosamine induces GibS expression, which in turn modifies the transcript levels of metabolic enzymes. |
format | Online Article Text |
id | pubmed-7366714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73667142020-07-21 A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron Ryan, Daniel Jenniches, Laura Reichardt, Sarah Barquist, Lars Westermann, Alexander J. Nat Commun Article Bacteria of the genus Bacteroides are common members of the human intestinal microbiota and important degraders of polysaccharides in the gut. Among them, the species Bacteroides thetaiotaomicron has emerged as the model organism for functional microbiota research. Here, we use differential RNA sequencing (dRNA-seq) to generate a single-nucleotide resolution transcriptome map of B. thetaiotaomicron grown under defined laboratory conditions. An online browser, called ‘Theta-Base’ (www.helmholtz-hiri.de/en/datasets/bacteroides), is launched to interrogate the obtained gene expression data and annotations of ~4500 transcription start sites, untranslated regions, operon structures, and 269 noncoding RNA elements. Among the latter is GibS, a conserved, 145 nt-long small RNA that is highly expressed in the presence of N-acetyl-D-glucosamine as sole carbon source. We use computational predictions and experimental data to determine the secondary structure of GibS and identify its target genes. Our results indicate that sensing of N-acetyl-D-glucosamine induces GibS expression, which in turn modifies the transcript levels of metabolic enzymes. Nature Publishing Group UK 2020-07-16 /pmc/articles/PMC7366714/ /pubmed/32678091 http://dx.doi.org/10.1038/s41467-020-17348-5 Text en © The Author(s) 2020 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 Ryan, Daniel Jenniches, Laura Reichardt, Sarah Barquist, Lars Westermann, Alexander J. A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title | A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title_full | A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title_fullStr | A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title_full_unstemmed | A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title_short | A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron |
title_sort | high-resolution transcriptome map identifies small rna regulation of metabolism in the gut microbe bacteroides thetaiotaomicron |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366714/ https://www.ncbi.nlm.nih.gov/pubmed/32678091 http://dx.doi.org/10.1038/s41467-020-17348-5 |
work_keys_str_mv | AT ryandaniel ahighresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT jennicheslaura ahighresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT reichardtsarah ahighresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT barquistlars ahighresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT westermannalexanderj ahighresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT ryandaniel highresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT jennicheslaura highresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT reichardtsarah highresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT barquistlars highresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron AT westermannalexanderj highresolutiontranscriptomemapidentifiessmallrnaregulationofmetabolisminthegutmicrobebacteroidesthetaiotaomicron |