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Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization
The SGI1‐family elements that are specifically mobilized by the IncA‐ and IncC‐family plasmids are important vehicles of antibiotic resistance among enteric bacteria. Although SGI1 exploits many plasmid‐derived conjugation and regulatory functions, the basic mobilization module of the island is unre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299015/ https://www.ncbi.nlm.nih.gov/pubmed/34784078 http://dx.doi.org/10.1111/mmi.14846 |
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author | Nagy, István Szabó, Mónika Hegyi, Anna Kiss, János |
author_facet | Nagy, István Szabó, Mónika Hegyi, Anna Kiss, János |
author_sort | Nagy, István |
collection | PubMed |
description | The SGI1‐family elements that are specifically mobilized by the IncA‐ and IncC‐family plasmids are important vehicles of antibiotic resistance among enteric bacteria. Although SGI1 exploits many plasmid‐derived conjugation and regulatory functions, the basic mobilization module of the island is unrelated to that of IncC plasmids. This module contains the oriT and encodes the mobilization proteins MpsA and MpsB, which belong to the tyrosine recombinases and not to relaxases. Here we report an additional, essential transfer factor of SGI1. This is a small RNA deriving from the 3′‐end of a primary RNA that can also serve as mRNA of ORF S022. The functional domain of this sRNA named sgm‐sRNA is encoded between the mpsA gene and the oriT of SGI1. Terminator‐like sequence near the promoter of the primary transcript possibly has a regulatory function in controlling the amount of full‐length primary RNA, which is converted to the active sgm‐sRNA through consecutive maturation steps influenced by the 5′‐end of the primary RNA. The mobilization module of SGI1 seems unique due to its atypical relaxase and the newly identified sgm‐sRNA, which is required for the horizontal transfer of the island but appears to act differently from classical regulatory sRNAs. |
format | Online Article Text |
id | pubmed-9299015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92990152022-07-21 Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization Nagy, István Szabó, Mónika Hegyi, Anna Kiss, János Mol Microbiol Research Articles The SGI1‐family elements that are specifically mobilized by the IncA‐ and IncC‐family plasmids are important vehicles of antibiotic resistance among enteric bacteria. Although SGI1 exploits many plasmid‐derived conjugation and regulatory functions, the basic mobilization module of the island is unrelated to that of IncC plasmids. This module contains the oriT and encodes the mobilization proteins MpsA and MpsB, which belong to the tyrosine recombinases and not to relaxases. Here we report an additional, essential transfer factor of SGI1. This is a small RNA deriving from the 3′‐end of a primary RNA that can also serve as mRNA of ORF S022. The functional domain of this sRNA named sgm‐sRNA is encoded between the mpsA gene and the oriT of SGI1. Terminator‐like sequence near the promoter of the primary transcript possibly has a regulatory function in controlling the amount of full‐length primary RNA, which is converted to the active sgm‐sRNA through consecutive maturation steps influenced by the 5′‐end of the primary RNA. The mobilization module of SGI1 seems unique due to its atypical relaxase and the newly identified sgm‐sRNA, which is required for the horizontal transfer of the island but appears to act differently from classical regulatory sRNAs. John Wiley and Sons Inc. 2021-11-25 2021-12 /pmc/articles/PMC9299015/ /pubmed/34784078 http://dx.doi.org/10.1111/mmi.14846 Text en © 2021 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Nagy, István Szabó, Mónika Hegyi, Anna Kiss, János Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title |
Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title_full |
Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title_fullStr |
Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title_full_unstemmed |
Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title_short |
Salmonella Genomic Island 1 requires a self‐encoded small RNA for mobilization |
title_sort | salmonella genomic island 1 requires a self‐encoded small rna for mobilization |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299015/ https://www.ncbi.nlm.nih.gov/pubmed/34784078 http://dx.doi.org/10.1111/mmi.14846 |
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