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Introducing the ArsR-Regulated Arsenic Stimulon

The microbial ars operon encodes the primary bacterial defense response to the environmental toxicant, arsenic. An important component of this operon is the arsR gene, which encodes ArsR, a member of the family of proteins categorized as DNA-binding transcriptional repressors. As currently documente...

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Autores principales: Rawle, Rachel, Saley, Tara C., Kang, Yoon-Suk, Wang, Qian, Walk, Seth, Bothner, Brian, McDermott, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7965956/
https://www.ncbi.nlm.nih.gov/pubmed/33746923
http://dx.doi.org/10.3389/fmicb.2021.630562
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author Rawle, Rachel
Saley, Tara C.
Kang, Yoon-Suk
Wang, Qian
Walk, Seth
Bothner, Brian
McDermott, Timothy R.
author_facet Rawle, Rachel
Saley, Tara C.
Kang, Yoon-Suk
Wang, Qian
Walk, Seth
Bothner, Brian
McDermott, Timothy R.
author_sort Rawle, Rachel
collection PubMed
description The microbial ars operon encodes the primary bacterial defense response to the environmental toxicant, arsenic. An important component of this operon is the arsR gene, which encodes ArsR, a member of the family of proteins categorized as DNA-binding transcriptional repressors. As currently documented, ArsR regulates its own expression as well as other genes in the same ars operon. This study examined the roles of four ArsR proteins in the well-developed model Gram-negative bacterium Agrobacterium tumefaciens 5A. RNASeq was used to compare and characterize gene expression profiles in ± arsenite-treated cells of the wild-type strain and in four different arsR mutants. We report that ArsR-controlled transcription regulation is truly global, extending well beyond the current ars operon model, and includes both repression as well as apparent activation effects. Many cellular functions are significantly influenced, including arsenic resistance, phosphate acquisition/metabolism, sugar transport, chemotaxis, copper tolerance, iron homeostasis, and many others. While there is evidence of some regulatory overlap, each ArsR exhibits its own regulatory profile. Furthermore, evidence of a regulatory hierarchy was observed; i.e. ArsR1 represses arsR4, ArsR4 activates arsR2, and ArsR2 represses arsR3. Additionally and unexpectedly, aioB (arsenite oxidase small subunit) expression was shown to be under partial positive control by ArsR2 and ArsR4. Summarizing, this study demonstrates the regulatory portfolio of arsenite-activated ArsR proteins and includes essentially all major cellular functions. The broad bandwidth of arsenic effects on microbial metabolism assists in explaining and understanding the full impact of arsenic in natural ecosystems, including the mammalian gut.
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spelling pubmed-79659562021-03-18 Introducing the ArsR-Regulated Arsenic Stimulon Rawle, Rachel Saley, Tara C. Kang, Yoon-Suk Wang, Qian Walk, Seth Bothner, Brian McDermott, Timothy R. Front Microbiol Microbiology The microbial ars operon encodes the primary bacterial defense response to the environmental toxicant, arsenic. An important component of this operon is the arsR gene, which encodes ArsR, a member of the family of proteins categorized as DNA-binding transcriptional repressors. As currently documented, ArsR regulates its own expression as well as other genes in the same ars operon. This study examined the roles of four ArsR proteins in the well-developed model Gram-negative bacterium Agrobacterium tumefaciens 5A. RNASeq was used to compare and characterize gene expression profiles in ± arsenite-treated cells of the wild-type strain and in four different arsR mutants. We report that ArsR-controlled transcription regulation is truly global, extending well beyond the current ars operon model, and includes both repression as well as apparent activation effects. Many cellular functions are significantly influenced, including arsenic resistance, phosphate acquisition/metabolism, sugar transport, chemotaxis, copper tolerance, iron homeostasis, and many others. While there is evidence of some regulatory overlap, each ArsR exhibits its own regulatory profile. Furthermore, evidence of a regulatory hierarchy was observed; i.e. ArsR1 represses arsR4, ArsR4 activates arsR2, and ArsR2 represses arsR3. Additionally and unexpectedly, aioB (arsenite oxidase small subunit) expression was shown to be under partial positive control by ArsR2 and ArsR4. Summarizing, this study demonstrates the regulatory portfolio of arsenite-activated ArsR proteins and includes essentially all major cellular functions. The broad bandwidth of arsenic effects on microbial metabolism assists in explaining and understanding the full impact of arsenic in natural ecosystems, including the mammalian gut. Frontiers Media S.A. 2021-03-03 /pmc/articles/PMC7965956/ /pubmed/33746923 http://dx.doi.org/10.3389/fmicb.2021.630562 Text en Copyright © 2021 Rawle, Saley, Kang, Wang, Walk, Bothner and McDermott. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Rawle, Rachel
Saley, Tara C.
Kang, Yoon-Suk
Wang, Qian
Walk, Seth
Bothner, Brian
McDermott, Timothy R.
Introducing the ArsR-Regulated Arsenic Stimulon
title Introducing the ArsR-Regulated Arsenic Stimulon
title_full Introducing the ArsR-Regulated Arsenic Stimulon
title_fullStr Introducing the ArsR-Regulated Arsenic Stimulon
title_full_unstemmed Introducing the ArsR-Regulated Arsenic Stimulon
title_short Introducing the ArsR-Regulated Arsenic Stimulon
title_sort introducing the arsr-regulated arsenic stimulon
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7965956/
https://www.ncbi.nlm.nih.gov/pubmed/33746923
http://dx.doi.org/10.3389/fmicb.2021.630562
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