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Genome-wide identification of Kanamycin B binding RNA in Escherichia coli
BACKGROUND: The aminoglycosides are established antibiotics that inhibit bacterial protein synthesis by binding to ribosomal RNA. Additional non-antibiotic aminoglycoside cellular functions have also been identified through aminoglycoside interactions with cellular RNAs. The full extent, however, of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018874/ https://www.ncbi.nlm.nih.gov/pubmed/36927548 http://dx.doi.org/10.1186/s12864-023-09234-3 |
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author | Chang, Yaowen Sun, Wenxia Murchie, Alastair I. H. Chen, Dongrong |
author_facet | Chang, Yaowen Sun, Wenxia Murchie, Alastair I. H. Chen, Dongrong |
author_sort | Chang, Yaowen |
collection | PubMed |
description | BACKGROUND: The aminoglycosides are established antibiotics that inhibit bacterial protein synthesis by binding to ribosomal RNA. Additional non-antibiotic aminoglycoside cellular functions have also been identified through aminoglycoside interactions with cellular RNAs. The full extent, however, of genome-wide aminoglycoside RNA interactions in Escherichia coli has not been determined. Here, we report genome-wide identification and verification of the aminoglycoside Kanamycin B binding to Escherichia coli RNAs. Immobilized Kanamycin B beads in pull-down assays were used for transcriptome-profiling analysis (RNA-seq). RESULTS: Over two hundred Kanamycin B binding RNAs were identified. Functional classification analysis of the RNA sequence related genes revealed a wide range of cellular functions. Small RNA fragments (ncRNA, tRNA and rRNA) or small mRNA was used to verify the binding with Kanamycin B in vitro. Kanamycin B and ibsC mRNA was analysed by chemical probing. CONCLUSIONS: The results will provide biochemical evidence and understanding of potential extra-antibiotic cellular functions of aminoglycosides in Escherichia coli. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09234-3. |
format | Online Article Text |
id | pubmed-10018874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100188742023-03-17 Genome-wide identification of Kanamycin B binding RNA in Escherichia coli Chang, Yaowen Sun, Wenxia Murchie, Alastair I. H. Chen, Dongrong BMC Genomics Research BACKGROUND: The aminoglycosides are established antibiotics that inhibit bacterial protein synthesis by binding to ribosomal RNA. Additional non-antibiotic aminoglycoside cellular functions have also been identified through aminoglycoside interactions with cellular RNAs. The full extent, however, of genome-wide aminoglycoside RNA interactions in Escherichia coli has not been determined. Here, we report genome-wide identification and verification of the aminoglycoside Kanamycin B binding to Escherichia coli RNAs. Immobilized Kanamycin B beads in pull-down assays were used for transcriptome-profiling analysis (RNA-seq). RESULTS: Over two hundred Kanamycin B binding RNAs were identified. Functional classification analysis of the RNA sequence related genes revealed a wide range of cellular functions. Small RNA fragments (ncRNA, tRNA and rRNA) or small mRNA was used to verify the binding with Kanamycin B in vitro. Kanamycin B and ibsC mRNA was analysed by chemical probing. CONCLUSIONS: The results will provide biochemical evidence and understanding of potential extra-antibiotic cellular functions of aminoglycosides in Escherichia coli. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09234-3. BioMed Central 2023-03-16 /pmc/articles/PMC10018874/ /pubmed/36927548 http://dx.doi.org/10.1186/s12864-023-09234-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chang, Yaowen Sun, Wenxia Murchie, Alastair I. H. Chen, Dongrong Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title | Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title_full | Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title_fullStr | Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title_full_unstemmed | Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title_short | Genome-wide identification of Kanamycin B binding RNA in Escherichia coli |
title_sort | genome-wide identification of kanamycin b binding rna in escherichia coli |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018874/ https://www.ncbi.nlm.nih.gov/pubmed/36927548 http://dx.doi.org/10.1186/s12864-023-09234-3 |
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