Cargando…

Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes

BACKGROUND: Multiple prokaryotic lineages use the arginine deiminase (ADI) pathway for anaerobic energy production by arginine degradation. The distribution of this pathway among eukaryotes has been thought to be very limited, with only two specialized groups living in low oxygen environments (Parab...

Descripción completa

Detalles Bibliográficos
Autores principales: Novák, Lukáš, Zubáčová, Zuzana, Karnkowska, Anna, Kolisko, Martin, Hroudová, Miluše, Stairs, Courtney W., Simpson, Alastair G. B., Keeling, Patrick J., Roger, Andrew J., Čepička, Ivan, Hampl, Vladimír
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052871/
https://www.ncbi.nlm.nih.gov/pubmed/27716026
http://dx.doi.org/10.1186/s12862-016-0771-4
_version_ 1782458304969048064
author Novák, Lukáš
Zubáčová, Zuzana
Karnkowska, Anna
Kolisko, Martin
Hroudová, Miluše
Stairs, Courtney W.
Simpson, Alastair G. B.
Keeling, Patrick J.
Roger, Andrew J.
Čepička, Ivan
Hampl, Vladimír
author_facet Novák, Lukáš
Zubáčová, Zuzana
Karnkowska, Anna
Kolisko, Martin
Hroudová, Miluše
Stairs, Courtney W.
Simpson, Alastair G. B.
Keeling, Patrick J.
Roger, Andrew J.
Čepička, Ivan
Hampl, Vladimír
author_sort Novák, Lukáš
collection PubMed
description BACKGROUND: Multiple prokaryotic lineages use the arginine deiminase (ADI) pathway for anaerobic energy production by arginine degradation. The distribution of this pathway among eukaryotes has been thought to be very limited, with only two specialized groups living in low oxygen environments (Parabasalia and Diplomonadida) known to possess the complete set of all three enzymes. We have performed an extensive survey of available sequence data in order to map the distribution of these enzymes among eukaryotes and to reconstruct their phylogenies. RESULTS: We have found genes for the complete pathway in almost all examined representatives of Metamonada, the anaerobic protist group that includes parabasalids and diplomonads. Phylogenetic analyses indicate the presence of the complete pathway in the last common ancestor of metamonads and heterologous transformation experiments suggest its cytosolic localization in the metamonad ancestor. Outside Metamonada, the complete pathway occurs rarely, nevertheless, it was found in representatives of most major eukaryotic clades. CONCLUSIONS: Phylogenetic relationships of complete pathways are consistent with the presence of the Archaea-derived ADI pathway in the last common ancestor of all eukaryotes, although other evolutionary scenarios remain possible. The presence of the incomplete set of enzymes is relatively common among eukaryotes and it may be related to the fact that these enzymes are involved in other cellular processes, such as the ornithine-urea cycle. Single protein phylogenies suggest that the evolutionary history of all three enzymes has been shaped by frequent gene losses and horizontal transfers, which may sometimes be connected with their diverse roles in cellular metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0771-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5052871
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-50528712016-10-06 Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes Novák, Lukáš Zubáčová, Zuzana Karnkowska, Anna Kolisko, Martin Hroudová, Miluše Stairs, Courtney W. Simpson, Alastair G. B. Keeling, Patrick J. Roger, Andrew J. Čepička, Ivan Hampl, Vladimír BMC Evol Biol Research Article BACKGROUND: Multiple prokaryotic lineages use the arginine deiminase (ADI) pathway for anaerobic energy production by arginine degradation. The distribution of this pathway among eukaryotes has been thought to be very limited, with only two specialized groups living in low oxygen environments (Parabasalia and Diplomonadida) known to possess the complete set of all three enzymes. We have performed an extensive survey of available sequence data in order to map the distribution of these enzymes among eukaryotes and to reconstruct their phylogenies. RESULTS: We have found genes for the complete pathway in almost all examined representatives of Metamonada, the anaerobic protist group that includes parabasalids and diplomonads. Phylogenetic analyses indicate the presence of the complete pathway in the last common ancestor of metamonads and heterologous transformation experiments suggest its cytosolic localization in the metamonad ancestor. Outside Metamonada, the complete pathway occurs rarely, nevertheless, it was found in representatives of most major eukaryotic clades. CONCLUSIONS: Phylogenetic relationships of complete pathways are consistent with the presence of the Archaea-derived ADI pathway in the last common ancestor of all eukaryotes, although other evolutionary scenarios remain possible. The presence of the incomplete set of enzymes is relatively common among eukaryotes and it may be related to the fact that these enzymes are involved in other cellular processes, such as the ornithine-urea cycle. Single protein phylogenies suggest that the evolutionary history of all three enzymes has been shaped by frequent gene losses and horizontal transfers, which may sometimes be connected with their diverse roles in cellular metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0771-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-06 /pmc/articles/PMC5052871/ /pubmed/27716026 http://dx.doi.org/10.1186/s12862-016-0771-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Novák, Lukáš
Zubáčová, Zuzana
Karnkowska, Anna
Kolisko, Martin
Hroudová, Miluše
Stairs, Courtney W.
Simpson, Alastair G. B.
Keeling, Patrick J.
Roger, Andrew J.
Čepička, Ivan
Hampl, Vladimír
Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title_full Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title_fullStr Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title_full_unstemmed Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title_short Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
title_sort arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052871/
https://www.ncbi.nlm.nih.gov/pubmed/27716026
http://dx.doi.org/10.1186/s12862-016-0771-4
work_keys_str_mv AT novaklukas argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT zubacovazuzana argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT karnkowskaanna argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT koliskomartin argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT hroudovamiluse argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT stairscourtneyw argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT simpsonalastairgb argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT keelingpatrickj argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT rogerandrewj argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT cepickaivan argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes
AT hamplvladimir argininedeiminasepathwayenzymesevolutionaryhistoryinmetamonadsandothereukaryotes