Cargando…

A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium

Bacterial sRNAs play an important role in regulating many cellular processes including metabolism, outer membrane homeostasis and virulence. Although sRNAs were initially found in intergenic regions, there is emerging evidence that protein coding regions of the genome are a rich reservoir of sRNAs....

Descripción completa

Detalles Bibliográficos
Autores principales: Ellis, Michael J., Trussler, Ryan S., Charles, Onella, Haniford, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435999/
https://www.ncbi.nlm.nih.gov/pubmed/28335027
http://dx.doi.org/10.1093/nar/gkx094
_version_ 1783237325306724352
author Ellis, Michael J.
Trussler, Ryan S.
Charles, Onella
Haniford, David B.
author_facet Ellis, Michael J.
Trussler, Ryan S.
Charles, Onella
Haniford, David B.
author_sort Ellis, Michael J.
collection PubMed
description Bacterial sRNAs play an important role in regulating many cellular processes including metabolism, outer membrane homeostasis and virulence. Although sRNAs were initially found in intergenic regions, there is emerging evidence that protein coding regions of the genome are a rich reservoir of sRNAs. Here we report that the 5΄UTR of IS200 transposase mRNA (tnpA) is processed to produce regulatory RNAs that affect expression of over 70 genes in Salmonella Typhimurium. We provide evidence that the tnpA derived sRNA base-pairs with invF mRNA to repress expression. As InvF is a transcriptional activator of SPI-1 encoded and other effector proteins, tnpA indirectly represses these genes. We show that deletion of IS200 elements in S. Typhimurium increases invasion in vitro and reduces growth rate, while over-expression of tnpA suppresses invasion. Our work indicates that tnpA acts as an sRNA ‘sponge’ that sets a threshold for activation of Salmonella pathogenicity island (SPI)-1 effector proteins and identifies a new class of ‘passenger gene’ for bacterial transposons, providing the first example of a bacterial transposon producing a regulatory RNA that controls host gene expression.
format Online
Article
Text
id pubmed-5435999
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-54359992017-05-22 A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium Ellis, Michael J. Trussler, Ryan S. Charles, Onella Haniford, David B. Nucleic Acids Res RNA Bacterial sRNAs play an important role in regulating many cellular processes including metabolism, outer membrane homeostasis and virulence. Although sRNAs were initially found in intergenic regions, there is emerging evidence that protein coding regions of the genome are a rich reservoir of sRNAs. Here we report that the 5΄UTR of IS200 transposase mRNA (tnpA) is processed to produce regulatory RNAs that affect expression of over 70 genes in Salmonella Typhimurium. We provide evidence that the tnpA derived sRNA base-pairs with invF mRNA to repress expression. As InvF is a transcriptional activator of SPI-1 encoded and other effector proteins, tnpA indirectly represses these genes. We show that deletion of IS200 elements in S. Typhimurium increases invasion in vitro and reduces growth rate, while over-expression of tnpA suppresses invasion. Our work indicates that tnpA acts as an sRNA ‘sponge’ that sets a threshold for activation of Salmonella pathogenicity island (SPI)-1 effector proteins and identifies a new class of ‘passenger gene’ for bacterial transposons, providing the first example of a bacterial transposon producing a regulatory RNA that controls host gene expression. Oxford University Press 2017-05-19 2017-02-21 /pmc/articles/PMC5435999/ /pubmed/28335027 http://dx.doi.org/10.1093/nar/gkx094 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle RNA
Ellis, Michael J.
Trussler, Ryan S.
Charles, Onella
Haniford, David B.
A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title_full A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title_fullStr A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title_full_unstemmed A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title_short A transposon-derived small RNA regulates gene expression in Salmonella Typhimurium
title_sort transposon-derived small rna regulates gene expression in salmonella typhimurium
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435999/
https://www.ncbi.nlm.nih.gov/pubmed/28335027
http://dx.doi.org/10.1093/nar/gkx094
work_keys_str_mv AT ellismichaelj atransposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT trusslerryans atransposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT charlesonella atransposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT haniforddavidb atransposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT ellismichaelj transposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT trusslerryans transposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT charlesonella transposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium
AT haniforddavidb transposonderivedsmallrnaregulatesgeneexpressioninsalmonellatyphimurium