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...
Autores principales: | , , |
---|---|
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 |