Cargando…

Differential synthesis of novel small protein times Salmonella virulence program

Gene organization in operons enables concerted transcription of functionally related genes and efficient control of cellular processes. Typically, an operon is transcribed as a polycistronic mRNA that is translated into corresponding proteins. Here, we identify a bicistronic operon transcribed as tw...

Descripción completa

Detalles Bibliográficos
Autores principales: Salvail, Hubert, Choi, Jeongjoon, Groisman, Eduardo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896665/
https://www.ncbi.nlm.nih.gov/pubmed/35245279
http://dx.doi.org/10.1371/journal.pgen.1010074
_version_ 1784663209363374080
author Salvail, Hubert
Choi, Jeongjoon
Groisman, Eduardo A.
author_facet Salvail, Hubert
Choi, Jeongjoon
Groisman, Eduardo A.
author_sort Salvail, Hubert
collection PubMed
description Gene organization in operons enables concerted transcription of functionally related genes and efficient control of cellular processes. Typically, an operon is transcribed as a polycistronic mRNA that is translated into corresponding proteins. Here, we identify a bicistronic operon transcribed as two mRNAs, yet only one allows translation of both genes. We establish that the novel gene ugtS forms an operon with virulence gene ugtL, an activator of the master virulence regulatory system PhoP/PhoQ in Salmonella enterica serovar Typhimurium. Only the longer ugtSugtL mRNA carries the ugtS ribosome binding site and therefore allows ugtS translation. Inside macrophages, the ugtSugtL mRNA species allowing translation of both genes is produced hours before that allowing translation solely of ugtL. The small protein UgtS controls the kinetics of PhoP phosphorylation by antagonizing UgtL activity, preventing premature activation of a critical virulence program. Moreover, S. enterica serovars that infect cold-blooded animals lack ugtS. Our results establish how foreign gene control of ancestral regulators enables pathogens to time their virulence programs.
format Online
Article
Text
id pubmed-8896665
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-88966652022-03-05 Differential synthesis of novel small protein times Salmonella virulence program Salvail, Hubert Choi, Jeongjoon Groisman, Eduardo A. PLoS Genet Research Article Gene organization in operons enables concerted transcription of functionally related genes and efficient control of cellular processes. Typically, an operon is transcribed as a polycistronic mRNA that is translated into corresponding proteins. Here, we identify a bicistronic operon transcribed as two mRNAs, yet only one allows translation of both genes. We establish that the novel gene ugtS forms an operon with virulence gene ugtL, an activator of the master virulence regulatory system PhoP/PhoQ in Salmonella enterica serovar Typhimurium. Only the longer ugtSugtL mRNA carries the ugtS ribosome binding site and therefore allows ugtS translation. Inside macrophages, the ugtSugtL mRNA species allowing translation of both genes is produced hours before that allowing translation solely of ugtL. The small protein UgtS controls the kinetics of PhoP phosphorylation by antagonizing UgtL activity, preventing premature activation of a critical virulence program. Moreover, S. enterica serovars that infect cold-blooded animals lack ugtS. Our results establish how foreign gene control of ancestral regulators enables pathogens to time their virulence programs. Public Library of Science 2022-03-04 /pmc/articles/PMC8896665/ /pubmed/35245279 http://dx.doi.org/10.1371/journal.pgen.1010074 Text en © 2022 Salvail et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Salvail, Hubert
Choi, Jeongjoon
Groisman, Eduardo A.
Differential synthesis of novel small protein times Salmonella virulence program
title Differential synthesis of novel small protein times Salmonella virulence program
title_full Differential synthesis of novel small protein times Salmonella virulence program
title_fullStr Differential synthesis of novel small protein times Salmonella virulence program
title_full_unstemmed Differential synthesis of novel small protein times Salmonella virulence program
title_short Differential synthesis of novel small protein times Salmonella virulence program
title_sort differential synthesis of novel small protein times salmonella virulence program
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896665/
https://www.ncbi.nlm.nih.gov/pubmed/35245279
http://dx.doi.org/10.1371/journal.pgen.1010074
work_keys_str_mv AT salvailhubert differentialsynthesisofnovelsmallproteintimessalmonellavirulenceprogram
AT choijeongjoon differentialsynthesisofnovelsmallproteintimessalmonellavirulenceprogram
AT groismaneduardoa differentialsynthesisofnovelsmallproteintimessalmonellavirulenceprogram