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A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium
Bacterial mRNAs often harbor upstream open reading frames (uORFs) in the 5′ untranslated regions (UTRs). Translation of the uORF usually affects downstream gene expression at the levels of transcription and/or translation initiation. Unlike other uORFs mostly located in the 5′ UTR, we discovered an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092293/ https://www.ncbi.nlm.nih.gov/pubmed/33849981 http://dx.doi.org/10.1128/mBio.03376-20 |
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author | Choi, Eunna Han, Yoontak Park, Shinae Koo, Hyojeong Lee, Jung-Shin Lee, Eun-Jin |
author_facet | Choi, Eunna Han, Yoontak Park, Shinae Koo, Hyojeong Lee, Jung-Shin Lee, Eun-Jin |
author_sort | Choi, Eunna |
collection | PubMed |
description | Bacterial mRNAs often harbor upstream open reading frames (uORFs) in the 5′ untranslated regions (UTRs). Translation of the uORF usually affects downstream gene expression at the levels of transcription and/or translation initiation. Unlike other uORFs mostly located in the 5′ UTR, we discovered an 8-amino-acid ORF, designated mgtQ, in the intergenic region between the mgtC virulence gene and the mgtB Mg(2+) transporter gene in the Salmonella mgtCBRU operon. Translation of mgtQ promotes downstream mgtB Mg(2+) transporter expression at the level of translation by releasing the ribosome-binding sequence of the mgtB gene that is sequestered in a translation-inhibitory stem-loop structure. Interestingly, mgtQ Asp2 and Glu5 codons that induce ribosome destabilization are required for mgtQ-mediated mgtB translation. Moreover, the mgtQ Asp and Glu codons-mediated mgtB translation is counteracted by the ribosomal subunit L31 that stabilizes ribosome. Substitution of the Asp2 and Glu5 codons in mgtQ decreases MgtB Mg(2+) transporter production and thus attenuates Salmonella virulence in mice, likely by limiting Mg(2+) acquisition during infection. |
format | Online Article Text |
id | pubmed-8092293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80922932021-05-04 A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium Choi, Eunna Han, Yoontak Park, Shinae Koo, Hyojeong Lee, Jung-Shin Lee, Eun-Jin mBio Research Article Bacterial mRNAs often harbor upstream open reading frames (uORFs) in the 5′ untranslated regions (UTRs). Translation of the uORF usually affects downstream gene expression at the levels of transcription and/or translation initiation. Unlike other uORFs mostly located in the 5′ UTR, we discovered an 8-amino-acid ORF, designated mgtQ, in the intergenic region between the mgtC virulence gene and the mgtB Mg(2+) transporter gene in the Salmonella mgtCBRU operon. Translation of mgtQ promotes downstream mgtB Mg(2+) transporter expression at the level of translation by releasing the ribosome-binding sequence of the mgtB gene that is sequestered in a translation-inhibitory stem-loop structure. Interestingly, mgtQ Asp2 and Glu5 codons that induce ribosome destabilization are required for mgtQ-mediated mgtB translation. Moreover, the mgtQ Asp and Glu codons-mediated mgtB translation is counteracted by the ribosomal subunit L31 that stabilizes ribosome. Substitution of the Asp2 and Glu5 codons in mgtQ decreases MgtB Mg(2+) transporter production and thus attenuates Salmonella virulence in mice, likely by limiting Mg(2+) acquisition during infection. American Society for Microbiology 2021-04-13 /pmc/articles/PMC8092293/ /pubmed/33849981 http://dx.doi.org/10.1128/mBio.03376-20 Text en Copyright © 2021 Choi et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Choi, Eunna Han, Yoontak Park, Shinae Koo, Hyojeong Lee, Jung-Shin Lee, Eun-Jin A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title | A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title_full | A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title_fullStr | A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title_full_unstemmed | A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title_short | A Translation-Aborting Small Open Reading Frame in the Intergenic Region Promotes Translation of a Mg(2+) Transporter in Salmonella Typhimurium |
title_sort | translation-aborting small open reading frame in the intergenic region promotes translation of a mg(2+) transporter in salmonella typhimurium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092293/ https://www.ncbi.nlm.nih.gov/pubmed/33849981 http://dx.doi.org/10.1128/mBio.03376-20 |
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