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Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions
Tight coordination between transcription and translation has long been recognized as the hallmark of gene expression in bacteria. In Escherichia coli cells, disruption of the transcription-translation coordination leads to the loss of transcription processivity via triggering Rho-mediated premature...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586808/ https://www.ncbi.nlm.nih.gov/pubmed/34805793 http://dx.doi.org/10.1016/j.isci.2021.103333 |
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author | Zhu, Manlu Mu, Haoyan Han, Fei Wang, Qian Dai, Xiongfeng |
author_facet | Zhu, Manlu Mu, Haoyan Han, Fei Wang, Qian Dai, Xiongfeng |
author_sort | Zhu, Manlu |
collection | PubMed |
description | Tight coordination between transcription and translation has long been recognized as the hallmark of gene expression in bacteria. In Escherichia coli cells, disruption of the transcription-translation coordination leads to the loss of transcription processivity via triggering Rho-mediated premature transcription termination. Here we quantitatively characterize the transcription and translation kinetics in Gram-positive model bacterium Bacillus subtilis. We found that the speed of transcription elongation is much faster than that of translation elongation in B. subtilis under various growth conditions. Moreover, a Rho-independent loss of transcription processivity occurs constitutively in several genes/operons but is not subject to translational control. When the transcription elongation is decelerated under poor nutrients, low temperature, or nucleotide depletion, the loss of transcription processivity is strongly enhanced, suggesting that its degree is modulated by the speed of transcription elongation. Our study reveals distinct design principles of gene expression in E. coli and B. subtilis. |
format | Online Article Text |
id | pubmed-8586808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85868082021-11-19 Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions Zhu, Manlu Mu, Haoyan Han, Fei Wang, Qian Dai, Xiongfeng iScience Article Tight coordination between transcription and translation has long been recognized as the hallmark of gene expression in bacteria. In Escherichia coli cells, disruption of the transcription-translation coordination leads to the loss of transcription processivity via triggering Rho-mediated premature transcription termination. Here we quantitatively characterize the transcription and translation kinetics in Gram-positive model bacterium Bacillus subtilis. We found that the speed of transcription elongation is much faster than that of translation elongation in B. subtilis under various growth conditions. Moreover, a Rho-independent loss of transcription processivity occurs constitutively in several genes/operons but is not subject to translational control. When the transcription elongation is decelerated under poor nutrients, low temperature, or nucleotide depletion, the loss of transcription processivity is strongly enhanced, suggesting that its degree is modulated by the speed of transcription elongation. Our study reveals distinct design principles of gene expression in E. coli and B. subtilis. Elsevier 2021-10-23 /pmc/articles/PMC8586808/ /pubmed/34805793 http://dx.doi.org/10.1016/j.isci.2021.103333 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Zhu, Manlu Mu, Haoyan Han, Fei Wang, Qian Dai, Xiongfeng Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title | Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title_full | Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title_fullStr | Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title_full_unstemmed | Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title_short | Quantitative analysis of asynchronous transcription-translation and transcription processivity in Bacillus subtilis under various growth conditions |
title_sort | quantitative analysis of asynchronous transcription-translation and transcription processivity in bacillus subtilis under various growth conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586808/ https://www.ncbi.nlm.nih.gov/pubmed/34805793 http://dx.doi.org/10.1016/j.isci.2021.103333 |
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