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Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis

The expression of rRNA is one of the most energetically demanding cellular processes and, as such, it must be stringently controlled. Here, we report that DNA topology, i.e., the level of DNA supercoiling, plays a role in the regulation of Bacillus subtilis σ(A)-dependent rRNA promoters in a growth...

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Autores principales: Sudzinová, Petra, Kambová, Milada, Ramaniuk, Olga, Benda, Martin, Šanderová, Hana, Krásný, Libor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824091/
https://www.ncbi.nlm.nih.gov/pubmed/33401387
http://dx.doi.org/10.3390/microorganisms9010087
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author Sudzinová, Petra
Kambová, Milada
Ramaniuk, Olga
Benda, Martin
Šanderová, Hana
Krásný, Libor
author_facet Sudzinová, Petra
Kambová, Milada
Ramaniuk, Olga
Benda, Martin
Šanderová, Hana
Krásný, Libor
author_sort Sudzinová, Petra
collection PubMed
description The expression of rRNA is one of the most energetically demanding cellular processes and, as such, it must be stringently controlled. Here, we report that DNA topology, i.e., the level of DNA supercoiling, plays a role in the regulation of Bacillus subtilis σ(A)-dependent rRNA promoters in a growth phase-dependent manner. The more negative DNA supercoiling in exponential phase stimulates transcription from rRNA promoters, and DNA relaxation in stationary phase contributes to cessation of their activity. Novobiocin treatment of B. subtilis cells relaxes DNA and decreases rRNA promoter activity despite an increase in the GTP level, a known positive regulator of B. subtilis rRNA promoters. Comparative analyses of steps during transcription initiation then reveal differences between rRNA promoters and a control promoter, Pveg, whose activity is less affected by changes in supercoiling. Additional data then show that DNA relaxation decreases transcription also from promoters dependent on alternative sigma factors σ(B), σ(D), σ(E), σ(F), and σ(H) with the exception of σ(N) where the trend is the opposite. To summarize, this study identifies DNA topology as a factor important (i) for the expression of rRNA in B. subtilis in response to nutrient availability in the environment, and (ii) for transcription activities of B. subtilis RNAP holoenzymes containing alternative sigma factors.
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spelling pubmed-78240912021-01-24 Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis Sudzinová, Petra Kambová, Milada Ramaniuk, Olga Benda, Martin Šanderová, Hana Krásný, Libor Microorganisms Article The expression of rRNA is one of the most energetically demanding cellular processes and, as such, it must be stringently controlled. Here, we report that DNA topology, i.e., the level of DNA supercoiling, plays a role in the regulation of Bacillus subtilis σ(A)-dependent rRNA promoters in a growth phase-dependent manner. The more negative DNA supercoiling in exponential phase stimulates transcription from rRNA promoters, and DNA relaxation in stationary phase contributes to cessation of their activity. Novobiocin treatment of B. subtilis cells relaxes DNA and decreases rRNA promoter activity despite an increase in the GTP level, a known positive regulator of B. subtilis rRNA promoters. Comparative analyses of steps during transcription initiation then reveal differences between rRNA promoters and a control promoter, Pveg, whose activity is less affected by changes in supercoiling. Additional data then show that DNA relaxation decreases transcription also from promoters dependent on alternative sigma factors σ(B), σ(D), σ(E), σ(F), and σ(H) with the exception of σ(N) where the trend is the opposite. To summarize, this study identifies DNA topology as a factor important (i) for the expression of rRNA in B. subtilis in response to nutrient availability in the environment, and (ii) for transcription activities of B. subtilis RNAP holoenzymes containing alternative sigma factors. MDPI 2021-01-01 /pmc/articles/PMC7824091/ /pubmed/33401387 http://dx.doi.org/10.3390/microorganisms9010087 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sudzinová, Petra
Kambová, Milada
Ramaniuk, Olga
Benda, Martin
Šanderová, Hana
Krásný, Libor
Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title_full Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title_fullStr Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title_full_unstemmed Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title_short Effects of DNA Topology on Transcription from rRNA Promoters in Bacillus subtilis
title_sort effects of dna topology on transcription from rrna promoters in bacillus subtilis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824091/
https://www.ncbi.nlm.nih.gov/pubmed/33401387
http://dx.doi.org/10.3390/microorganisms9010087
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