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S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum
The ubiGmccBA operon of Clostridium acetobutylicum is involved in methionine to cysteine conversion. We showed that its expression is controlled by a complex regulatory system combining several RNA-based mechanisms. Two functional convergent promoters associated with transcriptional antitermination...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566862/ https://www.ncbi.nlm.nih.gov/pubmed/18812398 http://dx.doi.org/10.1093/nar/gkn601 |
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author | André, Gaëlle Even, Sergine Putzer, Harald Burguière, Pierre Croux, Christian Danchin, Antoine Martin-Verstraete, Isabelle Soutourina, Olga |
author_facet | André, Gaëlle Even, Sergine Putzer, Harald Burguière, Pierre Croux, Christian Danchin, Antoine Martin-Verstraete, Isabelle Soutourina, Olga |
author_sort | André, Gaëlle |
collection | PubMed |
description | The ubiGmccBA operon of Clostridium acetobutylicum is involved in methionine to cysteine conversion. We showed that its expression is controlled by a complex regulatory system combining several RNA-based mechanisms. Two functional convergent promoters associated with transcriptional antitermination systems, a cysteine-specific T-box and an S-box riboswitch, are located upstream of and downstream from the ubiG operon, respectively. Several antisense RNAs were synthesized from the downstream S-box-dependent promoter, resulting in modulation of the level of ubiG transcript and of MccB activity. In contrast, the upstream T-box system did not appear to play a major role in regulation, leaving antisense transcription as the major regulatory mechanism for the ubiG operon. The abundance of sense and antisense transcripts was inversely correlated with the sulfur source availability. Deletion of the downstream promoter region completely abolished the sulfur-dependent control of the ubiG operon, and the expression of antisense transcripts in trans did not restore the regulation of the operon. Our data revealed important insights into the molecular mechanism of cis-antisense-mediated regulation, a control system only rarely observed in prokaryotes. We proposed a regulatory model in which the antisense RNA controlled the expression of the ubiG operon in cis via transcriptional interference at the ubiG locus. |
format | Text |
id | pubmed-2566862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25668622008-10-17 S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum André, Gaëlle Even, Sergine Putzer, Harald Burguière, Pierre Croux, Christian Danchin, Antoine Martin-Verstraete, Isabelle Soutourina, Olga Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The ubiGmccBA operon of Clostridium acetobutylicum is involved in methionine to cysteine conversion. We showed that its expression is controlled by a complex regulatory system combining several RNA-based mechanisms. Two functional convergent promoters associated with transcriptional antitermination systems, a cysteine-specific T-box and an S-box riboswitch, are located upstream of and downstream from the ubiG operon, respectively. Several antisense RNAs were synthesized from the downstream S-box-dependent promoter, resulting in modulation of the level of ubiG transcript and of MccB activity. In contrast, the upstream T-box system did not appear to play a major role in regulation, leaving antisense transcription as the major regulatory mechanism for the ubiG operon. The abundance of sense and antisense transcripts was inversely correlated with the sulfur source availability. Deletion of the downstream promoter region completely abolished the sulfur-dependent control of the ubiG operon, and the expression of antisense transcripts in trans did not restore the regulation of the operon. Our data revealed important insights into the molecular mechanism of cis-antisense-mediated regulation, a control system only rarely observed in prokaryotes. We proposed a regulatory model in which the antisense RNA controlled the expression of the ubiG operon in cis via transcriptional interference at the ubiG locus. Oxford University Press 2008-10 2008-09-23 /pmc/articles/PMC2566862/ /pubmed/18812398 http://dx.doi.org/10.1093/nar/gkn601 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics André, Gaëlle Even, Sergine Putzer, Harald Burguière, Pierre Croux, Christian Danchin, Antoine Martin-Verstraete, Isabelle Soutourina, Olga S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title | S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title_full | S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title_fullStr | S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title_full_unstemmed | S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title_short | S-box and T-box riboswitches and antisense RNA control a sulfur metabolic operon of Clostridium acetobutylicum |
title_sort | s-box and t-box riboswitches and antisense rna control a sulfur metabolic operon of clostridium acetobutylicum |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566862/ https://www.ncbi.nlm.nih.gov/pubmed/18812398 http://dx.doi.org/10.1093/nar/gkn601 |
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