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Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP

We here report the phylogenetic position of barthelonids, small anaerobic flagellates previously examined using light microscopy alone. Barthelona spp. were isolated from geographically distinct regions and we established five laboratory strains. Transcriptomic data generated from one Barthelona str...

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Autores principales: Yazaki, Euki, Kume, Keitaro, Shiratori, Takashi, Eglit, Yana, Tanifuji, Goro, Harada, Ryo, Simpson, Alastair G. B., Ishida, Ken-ichiro, Hashimoto, Tetsuo, Inagaki, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542792/
https://www.ncbi.nlm.nih.gov/pubmed/32873198
http://dx.doi.org/10.1098/rspb.2020.1538
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author Yazaki, Euki
Kume, Keitaro
Shiratori, Takashi
Eglit, Yana
Tanifuji, Goro
Harada, Ryo
Simpson, Alastair G. B.
Ishida, Ken-ichiro
Hashimoto, Tetsuo
Inagaki, Yuji
author_facet Yazaki, Euki
Kume, Keitaro
Shiratori, Takashi
Eglit, Yana
Tanifuji, Goro
Harada, Ryo
Simpson, Alastair G. B.
Ishida, Ken-ichiro
Hashimoto, Tetsuo
Inagaki, Yuji
author_sort Yazaki, Euki
collection PubMed
description We here report the phylogenetic position of barthelonids, small anaerobic flagellates previously examined using light microscopy alone. Barthelona spp. were isolated from geographically distinct regions and we established five laboratory strains. Transcriptomic data generated from one Barthelona strain (PAP020) were used for large-scale, multi-gene phylogenetic (phylogenomic) analyses. Our analyses robustly placed strain PAP020 at the base of the Fornicata clade, indicating that barthelonids represent a deep-branching metamonad clade. Considering the anaerobic/microaerophilic nature of barthelonids and preliminary electron microscopy observations on strain PAP020, we suspected that barthelonids possess functionally and structurally reduced mitochondria (i.e. mitochondrion-related organelles or MROs). The metabolic pathways localized in the MRO of strain PAP020 were predicted based on its transcriptomic data and compared with those in the MROs of fornicates. We here propose that strain PAP020 is incapable of generating ATP in the MRO, as no mitochondrial/MRO enzymes involved in substrate-level phosphorylation were detected. Instead, we detected a putative cytosolic ATP-generating enzyme (acetyl-CoA synthetase), suggesting that strain PAP020 depends on ATP generated in the cytosol. We propose two separate losses of substrate-level phosphorylation from the MRO in the clade containing barthelonids and (other) fornicates.
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spelling pubmed-75427922020-10-11 Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP Yazaki, Euki Kume, Keitaro Shiratori, Takashi Eglit, Yana Tanifuji, Goro Harada, Ryo Simpson, Alastair G. B. Ishida, Ken-ichiro Hashimoto, Tetsuo Inagaki, Yuji Proc Biol Sci Evolution We here report the phylogenetic position of barthelonids, small anaerobic flagellates previously examined using light microscopy alone. Barthelona spp. were isolated from geographically distinct regions and we established five laboratory strains. Transcriptomic data generated from one Barthelona strain (PAP020) were used for large-scale, multi-gene phylogenetic (phylogenomic) analyses. Our analyses robustly placed strain PAP020 at the base of the Fornicata clade, indicating that barthelonids represent a deep-branching metamonad clade. Considering the anaerobic/microaerophilic nature of barthelonids and preliminary electron microscopy observations on strain PAP020, we suspected that barthelonids possess functionally and structurally reduced mitochondria (i.e. mitochondrion-related organelles or MROs). The metabolic pathways localized in the MRO of strain PAP020 were predicted based on its transcriptomic data and compared with those in the MROs of fornicates. We here propose that strain PAP020 is incapable of generating ATP in the MRO, as no mitochondrial/MRO enzymes involved in substrate-level phosphorylation were detected. Instead, we detected a putative cytosolic ATP-generating enzyme (acetyl-CoA synthetase), suggesting that strain PAP020 depends on ATP generated in the cytosol. We propose two separate losses of substrate-level phosphorylation from the MRO in the clade containing barthelonids and (other) fornicates. The Royal Society 2020-09-09 2020-09-02 /pmc/articles/PMC7542792/ /pubmed/32873198 http://dx.doi.org/10.1098/rspb.2020.1538 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Yazaki, Euki
Kume, Keitaro
Shiratori, Takashi
Eglit, Yana
Tanifuji, Goro
Harada, Ryo
Simpson, Alastair G. B.
Ishida, Ken-ichiro
Hashimoto, Tetsuo
Inagaki, Yuji
Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title_full Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title_fullStr Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title_full_unstemmed Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title_short Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP
title_sort barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no atp
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542792/
https://www.ncbi.nlm.nih.gov/pubmed/32873198
http://dx.doi.org/10.1098/rspb.2020.1538
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