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Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation
Motility regulation plays a key role in prokaryotic responses to environmental stimuli. Here, we used a motility screen and selection to isolate hypermotile Haloferax volcanii mutants from a transposon insertion library. Whole genome sequencing revealed that hypermotile mutants were predominantly af...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824242/ https://www.ncbi.nlm.nih.gov/pubmed/33396553 http://dx.doi.org/10.3390/genes12010058 |
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author | Collins, Michiyah Afolayan, Simisola Igiraneza, Aime B. Schiller, Heather Krespan, Elise Beiting, Daniel P. Dyall-Smith, Mike Pfeiffer, Friedhelm Pohlschroder, Mechthild |
author_facet | Collins, Michiyah Afolayan, Simisola Igiraneza, Aime B. Schiller, Heather Krespan, Elise Beiting, Daniel P. Dyall-Smith, Mike Pfeiffer, Friedhelm Pohlschroder, Mechthild |
author_sort | Collins, Michiyah |
collection | PubMed |
description | Motility regulation plays a key role in prokaryotic responses to environmental stimuli. Here, we used a motility screen and selection to isolate hypermotile Haloferax volcanii mutants from a transposon insertion library. Whole genome sequencing revealed that hypermotile mutants were predominantly affected in two genes that encode HVO_1357 and HVO_2248. Alterations of these genes comprised not only transposon insertions but also secondary genome alterations. HVO_1357 contains a domain that was previously identified in the regulation of bacteriorhodopsin transcription, as well as other domains frequently found in two-component regulatory systems. The genes adjacent to hvo_1357 encode a sensor box histidine kinase and a response regulator, key players of a two-component regulatory system. None of the homologues of HVO_2248 have been characterized, nor does it contain any of the assigned InterPro domains. However, in a significant number of Haloferax species, the adjacent gene codes for a chemotaxis receptor/transducer. Our results provide a foundation for characterizing the root causes underlying Hfx. volcanii hypermotility. |
format | Online Article Text |
id | pubmed-7824242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78242422021-01-24 Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation Collins, Michiyah Afolayan, Simisola Igiraneza, Aime B. Schiller, Heather Krespan, Elise Beiting, Daniel P. Dyall-Smith, Mike Pfeiffer, Friedhelm Pohlschroder, Mechthild Genes (Basel) Article Motility regulation plays a key role in prokaryotic responses to environmental stimuli. Here, we used a motility screen and selection to isolate hypermotile Haloferax volcanii mutants from a transposon insertion library. Whole genome sequencing revealed that hypermotile mutants were predominantly affected in two genes that encode HVO_1357 and HVO_2248. Alterations of these genes comprised not only transposon insertions but also secondary genome alterations. HVO_1357 contains a domain that was previously identified in the regulation of bacteriorhodopsin transcription, as well as other domains frequently found in two-component regulatory systems. The genes adjacent to hvo_1357 encode a sensor box histidine kinase and a response regulator, key players of a two-component regulatory system. None of the homologues of HVO_2248 have been characterized, nor does it contain any of the assigned InterPro domains. However, in a significant number of Haloferax species, the adjacent gene codes for a chemotaxis receptor/transducer. Our results provide a foundation for characterizing the root causes underlying Hfx. volcanii hypermotility. MDPI 2020-12-31 /pmc/articles/PMC7824242/ /pubmed/33396553 http://dx.doi.org/10.3390/genes12010058 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Collins, Michiyah Afolayan, Simisola Igiraneza, Aime B. Schiller, Heather Krespan, Elise Beiting, Daniel P. Dyall-Smith, Mike Pfeiffer, Friedhelm Pohlschroder, Mechthild Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title | Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title_full | Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title_fullStr | Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title_full_unstemmed | Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title_short | Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in Haloferax volcanii, Suggesting Roles in Motility Regulation |
title_sort | mutations affecting hvo_1357 or hvo_2248 cause hypermotility in haloferax volcanii, suggesting roles in motility regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824242/ https://www.ncbi.nlm.nih.gov/pubmed/33396553 http://dx.doi.org/10.3390/genes12010058 |
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