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Chlamydial contribution to anaerobic metabolism during eukaryotic evolution

The origin of eukaryotes is a major open question in evolutionary biology. Multiple hypotheses posit that eukaryotes likely evolved from a syntrophic relationship between an archaeon and an alphaproteobacterium based on H(2) exchange. However, there are no strong indications that modern eukaryotic H...

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Autores principales: Stairs, Courtney W., Dharamshi, Jennah E., Tamarit, Daniel, Eme, Laura, Jørgensen, Steffen L., Spang, Anja, Ettema, Thijs J. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449678/
https://www.ncbi.nlm.nih.gov/pubmed/32923644
http://dx.doi.org/10.1126/sciadv.abb7258
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author Stairs, Courtney W.
Dharamshi, Jennah E.
Tamarit, Daniel
Eme, Laura
Jørgensen, Steffen L.
Spang, Anja
Ettema, Thijs J. G.
author_facet Stairs, Courtney W.
Dharamshi, Jennah E.
Tamarit, Daniel
Eme, Laura
Jørgensen, Steffen L.
Spang, Anja
Ettema, Thijs J. G.
author_sort Stairs, Courtney W.
collection PubMed
description The origin of eukaryotes is a major open question in evolutionary biology. Multiple hypotheses posit that eukaryotes likely evolved from a syntrophic relationship between an archaeon and an alphaproteobacterium based on H(2) exchange. However, there are no strong indications that modern eukaryotic H(2) metabolism originated from archaea or alphaproteobacteria. Here, we present evidence for the origin of H(2) metabolism genes in eukaryotes from an ancestor of the Anoxychlamydiales—a group of anaerobic chlamydiae, newly described here, from marine sediments. Among Chlamydiae, these bacteria uniquely encode genes for H(2) metabolism and other anaerobiosis-associated pathways. Phylogenetic analyses of several components of H(2) metabolism reveal that Anoxychlamydiales homologs are the closest relatives to eukaryotic sequences. We propose that an ancestor of the Anoxychlamydiales contributed these key genes during the evolution of eukaryotes, supporting a mosaic evolutionary origin of eukaryotic metabolism.
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spelling pubmed-74496782020-09-11 Chlamydial contribution to anaerobic metabolism during eukaryotic evolution Stairs, Courtney W. Dharamshi, Jennah E. Tamarit, Daniel Eme, Laura Jørgensen, Steffen L. Spang, Anja Ettema, Thijs J. G. Sci Adv Research Articles The origin of eukaryotes is a major open question in evolutionary biology. Multiple hypotheses posit that eukaryotes likely evolved from a syntrophic relationship between an archaeon and an alphaproteobacterium based on H(2) exchange. However, there are no strong indications that modern eukaryotic H(2) metabolism originated from archaea or alphaproteobacteria. Here, we present evidence for the origin of H(2) metabolism genes in eukaryotes from an ancestor of the Anoxychlamydiales—a group of anaerobic chlamydiae, newly described here, from marine sediments. Among Chlamydiae, these bacteria uniquely encode genes for H(2) metabolism and other anaerobiosis-associated pathways. Phylogenetic analyses of several components of H(2) metabolism reveal that Anoxychlamydiales homologs are the closest relatives to eukaryotic sequences. We propose that an ancestor of the Anoxychlamydiales contributed these key genes during the evolution of eukaryotes, supporting a mosaic evolutionary origin of eukaryotic metabolism. American Association for the Advancement of Science 2020-08-26 /pmc/articles/PMC7449678/ /pubmed/32923644 http://dx.doi.org/10.1126/sciadv.abb7258 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Stairs, Courtney W.
Dharamshi, Jennah E.
Tamarit, Daniel
Eme, Laura
Jørgensen, Steffen L.
Spang, Anja
Ettema, Thijs J. G.
Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title_full Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title_fullStr Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title_full_unstemmed Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title_short Chlamydial contribution to anaerobic metabolism during eukaryotic evolution
title_sort chlamydial contribution to anaerobic metabolism during eukaryotic evolution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449678/
https://www.ncbi.nlm.nih.gov/pubmed/32923644
http://dx.doi.org/10.1126/sciadv.abb7258
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