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Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes
L. Novák, Z. Zubáčová, A. Karnkowska, M. Kolisko, M. Hroudová, CW. Stairs, AG. Simpson, PJ. Keeling, AJ. Roger, I. Čepička, V. Hampl,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
NLK
BioMedCentral Open Access
od 2001
Directory of Open Access Journals
od 2001
Free Medical Journals
od 2001
PubMed Central
od 2001 do 2020
Europe PubMed Central
od 2001
ProQuest Central
od 2009-01-01 do 2020-01-31
Open Access Digital Library
od 2001-02-01
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2001-01-01
Medline Complete (EBSCOhost)
od 2001-01-01 do 2020-12-29
Health & Medicine (ProQuest)
od 2009-01-01 do 2020-01-31
ROAD: Directory of Open Access Scholarly Resources
od 2001 do 2021
- MeSH
- Archaea metabolismus MeSH
- arginin metabolismus MeSH
- Diplomonadida enzymologie MeSH
- Eukaryota klasifikace genetika metabolismus MeSH
- fylogeneze MeSH
- hydrolasy metabolismus MeSH
- metabolické sítě a dráhy * MeSH
- molekulární evoluce * MeSH
- Publikační typ
- časopisecké články MeSH
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.
Department of Biochemistry and Molecular Biology Dalhousie University Halifax Canada
Department of Biology Dalhousie University Halifax Canada
Department of Botany University of British Columbia Vancouver Canada
Department of Parasitology Charles University Faculty of Science Prague Czech Republic
Department of Zoology Charles University Faculty of Science Prague Czech Republic
Institute of Molecular Genetics Academy of Sciences of the Czech Republic Prague Czech Republic
Citace poskytuje Crossref.org
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- $a 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.
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