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Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis

Under hypoxic conditions, some organisms use an electron transport chain consisting of only complex I and II (CII) to generate the proton gradient essential for ATP production. In these cases, CII functions as a fumarate reductase that accepts electrons from a low electron potential quinol, rhodoqui...

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Autores principales: Stairs, Courtney W, Eme, Laura, Muñoz-Gómez, Sergio A, Cohen, Alejandro, Dellaire, Graham, Shepherd, Jennifer N, Fawcett, James P, Roger, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953543/
https://www.ncbi.nlm.nih.gov/pubmed/29697049
http://dx.doi.org/10.7554/eLife.34292
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author Stairs, Courtney W
Eme, Laura
Muñoz-Gómez, Sergio A
Cohen, Alejandro
Dellaire, Graham
Shepherd, Jennifer N
Fawcett, James P
Roger, Andrew J
author_facet Stairs, Courtney W
Eme, Laura
Muñoz-Gómez, Sergio A
Cohen, Alejandro
Dellaire, Graham
Shepherd, Jennifer N
Fawcett, James P
Roger, Andrew J
author_sort Stairs, Courtney W
collection PubMed
description Under hypoxic conditions, some organisms use an electron transport chain consisting of only complex I and II (CII) to generate the proton gradient essential for ATP production. In these cases, CII functions as a fumarate reductase that accepts electrons from a low electron potential quinol, rhodoquinol (RQ). To clarify the origins of RQ-mediated fumarate reduction in eukaryotes, we investigated the origin and function of rquA, a gene encoding an RQ biosynthetic enzyme. RquA is very patchily distributed across eukaryotes and bacteria adapted to hypoxia. Phylogenetic analyses suggest lateral gene transfer (LGT) of rquA from bacteria to eukaryotes occurred at least twice and the gene was transferred multiple times amongst protists. We demonstrate that RquA functions in the mitochondrion-related organelles of the anaerobic protist Pygsuia and is correlated with the presence of RQ. These analyses reveal the role of gene transfer in the evolutionary remodeling of mitochondria in adaptation to hypoxia.
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spelling pubmed-59535432018-05-16 Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis Stairs, Courtney W Eme, Laura Muñoz-Gómez, Sergio A Cohen, Alejandro Dellaire, Graham Shepherd, Jennifer N Fawcett, James P Roger, Andrew J eLife Evolutionary Biology Under hypoxic conditions, some organisms use an electron transport chain consisting of only complex I and II (CII) to generate the proton gradient essential for ATP production. In these cases, CII functions as a fumarate reductase that accepts electrons from a low electron potential quinol, rhodoquinol (RQ). To clarify the origins of RQ-mediated fumarate reduction in eukaryotes, we investigated the origin and function of rquA, a gene encoding an RQ biosynthetic enzyme. RquA is very patchily distributed across eukaryotes and bacteria adapted to hypoxia. Phylogenetic analyses suggest lateral gene transfer (LGT) of rquA from bacteria to eukaryotes occurred at least twice and the gene was transferred multiple times amongst protists. We demonstrate that RquA functions in the mitochondrion-related organelles of the anaerobic protist Pygsuia and is correlated with the presence of RQ. These analyses reveal the role of gene transfer in the evolutionary remodeling of mitochondria in adaptation to hypoxia. eLife Sciences Publications, Ltd 2018-04-26 /pmc/articles/PMC5953543/ /pubmed/29697049 http://dx.doi.org/10.7554/eLife.34292 Text en © 2018, Stairs et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Stairs, Courtney W
Eme, Laura
Muñoz-Gómez, Sergio A
Cohen, Alejandro
Dellaire, Graham
Shepherd, Jennifer N
Fawcett, James P
Roger, Andrew J
Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title_full Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title_fullStr Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title_full_unstemmed Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title_short Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
title_sort microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953543/
https://www.ncbi.nlm.nih.gov/pubmed/29697049
http://dx.doi.org/10.7554/eLife.34292
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