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Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli
The regulatory function of many bacterial small RNAs (sRNAs) requires the binding of the RNA chaperone Hfq to the 3′ portion of the sRNA intrinsic terminator, and therefore sRNA signaling might be regulated by modulating its terminator. Here, using a multicopy screen developed with the terminator of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9765468/ https://www.ncbi.nlm.nih.gov/pubmed/36226957 http://dx.doi.org/10.1128/mbio.02371-22 |
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author | Morita, Teppei Majdalani, Nadim Miura, Masahiro C. Inose, Rerina Oshima, Taku Tomita, Masaru Kanai, Akio Gottesman, Susan |
author_facet | Morita, Teppei Majdalani, Nadim Miura, Masahiro C. Inose, Rerina Oshima, Taku Tomita, Masaru Kanai, Akio Gottesman, Susan |
author_sort | Morita, Teppei |
collection | PubMed |
description | The regulatory function of many bacterial small RNAs (sRNAs) requires the binding of the RNA chaperone Hfq to the 3′ portion of the sRNA intrinsic terminator, and therefore sRNA signaling might be regulated by modulating its terminator. Here, using a multicopy screen developed with the terminator of sRNA SgrS, we identified an sRNA gene (cyaR) and three protein-coding genes (cspD, ygjH, and rof) that attenuate SgrS termination in Escherichia coli. Analyses of CyaR and YgjH, a putative tRNA binding protein, suggested that the CyaR activity was indirect and the effect of YgjH was moderate. Overproduction of the protein attenuators CspD and Rof resulted in more frequent readthrough at terminators of SgrS and two other sRNAs, and regulation by SgrS of target mRNAs was reduced. The effect of Rof, a known inhibitor of Rho, was mimicked by bicyclomycin or by a rho mutant, suggesting an unexpected role for Rho in sRNA termination. CspD, a member of the cold shock protein family, bound both terminated and readthrough transcripts, stabilizing them and attenuating termination. By RNA sequencing analysis of the CspD overexpression strain, we found global effects of CspD on gene expression across some termination sites. We further demonstrated effects of endogenous CspD under slow growth conditions where cspD is highly expressed. These findings provided evidence of changes in the efficiency of intrinsic termination, confirming this as an additional layer of the regulation of sRNA signaling. |
format | Online Article Text |
id | pubmed-9765468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-97654682022-12-21 Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli Morita, Teppei Majdalani, Nadim Miura, Masahiro C. Inose, Rerina Oshima, Taku Tomita, Masaru Kanai, Akio Gottesman, Susan mBio Research Article The regulatory function of many bacterial small RNAs (sRNAs) requires the binding of the RNA chaperone Hfq to the 3′ portion of the sRNA intrinsic terminator, and therefore sRNA signaling might be regulated by modulating its terminator. Here, using a multicopy screen developed with the terminator of sRNA SgrS, we identified an sRNA gene (cyaR) and three protein-coding genes (cspD, ygjH, and rof) that attenuate SgrS termination in Escherichia coli. Analyses of CyaR and YgjH, a putative tRNA binding protein, suggested that the CyaR activity was indirect and the effect of YgjH was moderate. Overproduction of the protein attenuators CspD and Rof resulted in more frequent readthrough at terminators of SgrS and two other sRNAs, and regulation by SgrS of target mRNAs was reduced. The effect of Rof, a known inhibitor of Rho, was mimicked by bicyclomycin or by a rho mutant, suggesting an unexpected role for Rho in sRNA termination. CspD, a member of the cold shock protein family, bound both terminated and readthrough transcripts, stabilizing them and attenuating termination. By RNA sequencing analysis of the CspD overexpression strain, we found global effects of CspD on gene expression across some termination sites. We further demonstrated effects of endogenous CspD under slow growth conditions where cspD is highly expressed. These findings provided evidence of changes in the efficiency of intrinsic termination, confirming this as an additional layer of the regulation of sRNA signaling. American Society for Microbiology 2022-10-13 /pmc/articles/PMC9765468/ /pubmed/36226957 http://dx.doi.org/10.1128/mbio.02371-22 Text en Copyright © 2022 Morita 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 Morita, Teppei Majdalani, Nadim Miura, Masahiro C. Inose, Rerina Oshima, Taku Tomita, Masaru Kanai, Akio Gottesman, Susan Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title | Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title_full | Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title_fullStr | Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title_full_unstemmed | Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title_short | Identification of Attenuators of Transcriptional Termination: Implications for RNA Regulation in Escherichia coli |
title_sort | identification of attenuators of transcriptional termination: implications for rna regulation in escherichia coli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9765468/ https://www.ncbi.nlm.nih.gov/pubmed/36226957 http://dx.doi.org/10.1128/mbio.02371-22 |
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