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Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters
Regulation of tetralin biodegradation operons is one of the examples of unconventional LysR-type mediated transcriptional regulation. ThnR activates transcription from two divergent and closely located promoters P(B) and P(C). Although ThnR activates each promoter independently, transcription from e...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834489/ https://www.ncbi.nlm.nih.gov/pubmed/27087658 http://dx.doi.org/10.1038/srep24538 |
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author | Rivas-Marín, Elena Floriano, Belén Santero, Eduardo |
author_facet | Rivas-Marín, Elena Floriano, Belén Santero, Eduardo |
author_sort | Rivas-Marín, Elena |
collection | PubMed |
description | Regulation of tetralin biodegradation operons is one of the examples of unconventional LysR-type mediated transcriptional regulation. ThnR activates transcription from two divergent and closely located promoters P(B) and P(C). Although ThnR activates each promoter independently, transcription from each one increases when both promoters are together. Mutational analysis of the intergenic region shows that cooperative transcription is achieved through formation of a ThnR complex when bound to its respective sites at each promoter, via formation of a DNA loop. Mutations also defined ThnR contact sites that are important for independent transcriptional activation at each promoter. A mutation at the P(B) promoter region, which abolishes its independent transcription, does not affect at all P(B) transcription in the presence of the divergent promoter P(C), thus indicating that the complex formed via DNA loop can compensate for the deficiencies in the correct protein-DNA interaction at one of the promoters. Combination of mutations in both promoters identifies a region at P(C) that is not important for its independent transcription but it is essential for cooperative transcription from both promoters. This work provides new insights into the diversity and complexity of activation mechanisms used by the most abundant type of bacterial transcriptional regulators. |
format | Online Article Text |
id | pubmed-4834489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48344892016-04-27 Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters Rivas-Marín, Elena Floriano, Belén Santero, Eduardo Sci Rep Article Regulation of tetralin biodegradation operons is one of the examples of unconventional LysR-type mediated transcriptional regulation. ThnR activates transcription from two divergent and closely located promoters P(B) and P(C). Although ThnR activates each promoter independently, transcription from each one increases when both promoters are together. Mutational analysis of the intergenic region shows that cooperative transcription is achieved through formation of a ThnR complex when bound to its respective sites at each promoter, via formation of a DNA loop. Mutations also defined ThnR contact sites that are important for independent transcriptional activation at each promoter. A mutation at the P(B) promoter region, which abolishes its independent transcription, does not affect at all P(B) transcription in the presence of the divergent promoter P(C), thus indicating that the complex formed via DNA loop can compensate for the deficiencies in the correct protein-DNA interaction at one of the promoters. Combination of mutations in both promoters identifies a region at P(C) that is not important for its independent transcription but it is essential for cooperative transcription from both promoters. This work provides new insights into the diversity and complexity of activation mechanisms used by the most abundant type of bacterial transcriptional regulators. Nature Publishing Group 2016-04-18 /pmc/articles/PMC4834489/ /pubmed/27087658 http://dx.doi.org/10.1038/srep24538 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Rivas-Marín, Elena Floriano, Belén Santero, Eduardo Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title | Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title_full | Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title_fullStr | Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title_full_unstemmed | Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title_short | Genetic dissection of independent and cooperative transcriptional activation by the LysR-type activator ThnR at close divergent promoters |
title_sort | genetic dissection of independent and cooperative transcriptional activation by the lysr-type activator thnr at close divergent promoters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834489/ https://www.ncbi.nlm.nih.gov/pubmed/27087658 http://dx.doi.org/10.1038/srep24538 |
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