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A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance

We have previously generated four replicate populations of ionizing radiation (IR)-resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS am...

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Autores principales: Bruckbauer, Steven T., Trimarco, Joseph D., Henry, Camille, Wood, Elizabeth A., Battista, John R., Cox, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343905/
https://www.ncbi.nlm.nih.gov/pubmed/30673695
http://dx.doi.org/10.1371/journal.pone.0199482
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author Bruckbauer, Steven T.
Trimarco, Joseph D.
Henry, Camille
Wood, Elizabeth A.
Battista, John R.
Cox, Michael M.
author_facet Bruckbauer, Steven T.
Trimarco, Joseph D.
Henry, Camille
Wood, Elizabeth A.
Battista, John R.
Cox, Michael M.
author_sort Bruckbauer, Steven T.
collection PubMed
description We have previously generated four replicate populations of ionizing radiation (IR)-resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS amelioration, and cell wall metabolism were prominent. Three mutations involved in DNA repair explained the IR resistance phenotype in one population, and similar DNA repair mutations were prominent in two others. The remaining population, IR-3-20, had no mutations in the key DNA repair proteins, suggesting that it had taken a different evolutionary path to IR resistance. Here, we present evidence that a variant of the anaerobic metabolism transcription factor FNR, unique to and isolated from population IR-3-20, plays a role in IR resistance. The F186I allele of FNR exhibits a diminished ability to activate transcription from FNR-activatable promoters, and furthermore reduces levels of intracellular ROS. The FNR F186I variant is apparently capable of enhancing resistance to IR under chronic irradiation conditions, but does not increase cell survival when exposed to acute irradiation. Our results underline the importance of dose rate on cell survival of IR exposure.
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spelling pubmed-63439052019-02-02 A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance Bruckbauer, Steven T. Trimarco, Joseph D. Henry, Camille Wood, Elizabeth A. Battista, John R. Cox, Michael M. PLoS One Research Article We have previously generated four replicate populations of ionizing radiation (IR)-resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS amelioration, and cell wall metabolism were prominent. Three mutations involved in DNA repair explained the IR resistance phenotype in one population, and similar DNA repair mutations were prominent in two others. The remaining population, IR-3-20, had no mutations in the key DNA repair proteins, suggesting that it had taken a different evolutionary path to IR resistance. Here, we present evidence that a variant of the anaerobic metabolism transcription factor FNR, unique to and isolated from population IR-3-20, plays a role in IR resistance. The F186I allele of FNR exhibits a diminished ability to activate transcription from FNR-activatable promoters, and furthermore reduces levels of intracellular ROS. The FNR F186I variant is apparently capable of enhancing resistance to IR under chronic irradiation conditions, but does not increase cell survival when exposed to acute irradiation. Our results underline the importance of dose rate on cell survival of IR exposure. Public Library of Science 2019-01-23 /pmc/articles/PMC6343905/ /pubmed/30673695 http://dx.doi.org/10.1371/journal.pone.0199482 Text en © 2019 Bruckbauer et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bruckbauer, Steven T.
Trimarco, Joseph D.
Henry, Camille
Wood, Elizabeth A.
Battista, John R.
Cox, Michael M.
A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title_full A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title_fullStr A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title_full_unstemmed A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title_short A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance
title_sort variant of the escherichia coli anaerobic transcription factor fnr exhibiting diminished promoter activation function enhances ionizing radiation resistance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343905/
https://www.ncbi.nlm.nih.gov/pubmed/30673695
http://dx.doi.org/10.1371/journal.pone.0199482
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