Gerbod D., Noël, C., Edgcomb,
V.P., Vaòáèová, S., Wintjens, R., Tachezy, J., Sogin, M.L., Viscogliosi, E. 2001.
Phylogenetic relationships of fumarase genes from trichomonad species. Molecular
Biology and Evolution 18:1574-1584
Keywords
Parabasala, trichomonads, fumarase, gene expression, protein evolution, molecular
phylogeny SUBUNIT RIBOSOMAL-RNA, ESCHERICHIA-COLI, GLYCERALDEHYDE-3-PHOSPHATE
DEHYDROGENASE, MOLECULAR CHARACTERIZATION, PROTIST TRICHOMONAS, TREE TOPOLOGIES,
PROTEIN IMPORT, ACTIVE-SITE, VAGINALIS, EVOLUTION
Abstract:
Class II fumarase sequences were obtained by polymerase chain reaction from five
trichomonad species. All residues known to be highly conserved in this enzyme
were present. Nuclear run-on assays showed that one of the two genes identified
in Tritrichomonas foetus was expressed, whereas no fumarase transcripts were detected
in the a related species Trichomonas vaginalis. These findings corroborate previous
biochemical data. Fumarase genes were also expressed in Monocercomonas sp. and
Tetratrichomonas gallinarum but not in Pentatrichomonas hominis, Trichomonas gallinae,
Trichomonas tenax, and Trichomitus batrachorum under the culture conditions used.
Molecular trees inferred by likelihood methods reveal that trichomonad sequences
have no affinity to described class II fumarase genes from other eukaryotes. The
absence of functional mitochondria in protists such as trichomonads suggests that
they diverged from other eukaryotes prior to the alpha-proteobacterial symbiosis
that led to mitochondria. Furthermore, they are basal to other eukaryotes in rRNA
analyses. However, support for the early-branching status of trichomonads and
other amitochondriate protists based on phylogenetic analyses of multiple data
sets has been equivocal. Although the presence of hydrogenosomes suggests that
trichomonads once had mitochondria, their class II iron-independent fumarase sequences
differ markedly from those of other mitochondriate eukaryotes. All of the class
II fumarase genes described from other eukaryotes are of apparent alpha-proteobacterial
origin and hence a marker of mitochondrial evolution. In contrast, the class II
fumarase from trichomonads emerges among other eubacterial homologs. This is intriguing
evidence for an independent acquisition of these genes in trichomonads apart from
the mitochondrial endosymbiosis event that gave rise to the form present in other
eukaryotes. The ancestral trichomonad class II fumarase may represent a prokaryotic
form that was replaced in other eukaryotes after the divergence of trichomonads
with the movement of endosymbiont genes into the nucleus. Alternatively, it may
have been acquired via a separate endosymbiotic event or lateral gene transfer.
ISSN 0737-4038
IF 5,298
USA