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Activation by NarL at the Escherichia coli ogt promoter
The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which control...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419079/ https://www.ncbi.nlm.nih.gov/pubmed/32662815 http://dx.doi.org/10.1042/BCJ20200408 |
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author | Ruanto, Patcharawarin Chismon, David L. Hothersall, Joanne Godfrey, Rita E. Lee, David J. Busby, Stephen J. W. Browning, Douglas F. |
author_facet | Ruanto, Patcharawarin Chismon, David L. Hothersall, Joanne Godfrey, Rita E. Lee, David J. Busby, Stephen J. W. Browning, Douglas F. |
author_sort | Ruanto, Patcharawarin |
collection | PubMed |
description | The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which controls the expression of an O(6)-alkylguanine-DNA-alkyltransferase, is dependent on NarL binding to two DNA targets centred at positions −44.5 and −77.5 upstream from the transcript start. Here, we describe ogt promoter derivatives that can be activated solely by NarL binding either at position −44.5 or position −77.5. We show that NarL can also activate the ogt promoter when located at position −67.5. We present data to argue that NarL-dependent activation of transcript initiation at the ogt promoter results from a direct interaction between NarL and a determinant in the C-terminal domain of the RNA polymerase α subunit. Footprinting experiments show that, at the −44.5 promoter, NarL and the C-terminal domain of the RNA polymerase α subunit bind to opposite faces of promoter DNA, suggesting an unusual mechanism of transcription activation. Our work suggests new organisations for activator-dependent transcription at promoters and future applications for biotechnology. |
format | Online Article Text |
id | pubmed-7419079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74190792020-08-19 Activation by NarL at the Escherichia coli ogt promoter Ruanto, Patcharawarin Chismon, David L. Hothersall, Joanne Godfrey, Rita E. Lee, David J. Busby, Stephen J. W. Browning, Douglas F. Biochem J Gene Expression & Regulation The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which controls the expression of an O(6)-alkylguanine-DNA-alkyltransferase, is dependent on NarL binding to two DNA targets centred at positions −44.5 and −77.5 upstream from the transcript start. Here, we describe ogt promoter derivatives that can be activated solely by NarL binding either at position −44.5 or position −77.5. We show that NarL can also activate the ogt promoter when located at position −67.5. We present data to argue that NarL-dependent activation of transcript initiation at the ogt promoter results from a direct interaction between NarL and a determinant in the C-terminal domain of the RNA polymerase α subunit. Footprinting experiments show that, at the −44.5 promoter, NarL and the C-terminal domain of the RNA polymerase α subunit bind to opposite faces of promoter DNA, suggesting an unusual mechanism of transcription activation. Our work suggests new organisations for activator-dependent transcription at promoters and future applications for biotechnology. Portland Press Ltd. 2020-08-14 2020-08-07 /pmc/articles/PMC7419079/ /pubmed/32662815 http://dx.doi.org/10.1042/BCJ20200408 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Birmingham in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC. |
spellingShingle | Gene Expression & Regulation Ruanto, Patcharawarin Chismon, David L. Hothersall, Joanne Godfrey, Rita E. Lee, David J. Busby, Stephen J. W. Browning, Douglas F. Activation by NarL at the Escherichia coli ogt promoter |
title | Activation by NarL at the Escherichia coli ogt promoter |
title_full | Activation by NarL at the Escherichia coli ogt promoter |
title_fullStr | Activation by NarL at the Escherichia coli ogt promoter |
title_full_unstemmed | Activation by NarL at the Escherichia coli ogt promoter |
title_short | Activation by NarL at the Escherichia coli ogt promoter |
title_sort | activation by narl at the escherichia coli ogt promoter |
topic | Gene Expression & Regulation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419079/ https://www.ncbi.nlm.nih.gov/pubmed/32662815 http://dx.doi.org/10.1042/BCJ20200408 |
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