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Fe-S Cluster Assembly in Oxymonads and Related Protists
Vojtech Vacek1, Lukáš V F Novák1, Sebastian C Treitli1
1Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Vestec, Czech Republic.
Molecular Biology and Evolution
|September 6, 2018
Summary
The SUF iron-sulfur (Fe-S) cluster pathway replaced the mitochondrial ISC pathway in oxymonads, enabling the loss of mitochondria. This evolutionary switch predates their common ancestor and involves fused SufDSU proteins.
Area of Science:
- Evolutionary biology
- Microbiology
- Biochemistry
Background:
- Monocercomonoides exilis, an oxymonad, is the first known eukaryote lacking mitochondria.
- Mitochondrial loss may have been facilitated by acquiring the prokaryotic SUF iron-sulfur (Fe-S) cluster assembly pathway, rendering the mitochondrial ISC pathway obsolete.
Purpose of the Study:
- To investigate the presence and distribution of Fe-S cluster biosynthesis pathways in oxymonads and related Preaxostyla species.
- To understand the evolutionary history and potential prokaryotic donors of the SUF pathway in these organisms.
Main Methods:
- Genomic and transcriptomic data analysis of six oxymonad species and relatives.
- Phylogenetic analyses to identify Fe-S cluster biosynthesis enzymes (ISC and SUF pathways).
- Examination of gene fusions, specifically SufDSU.
Main Results:
- No studied oxymonad or Preaxostyla species possesses the mitochondrial ISC pathway.
- All examined species contain the SUF pathway, indicating its acquisition preceded their last common ancestor.
- SufDSU proteins are fused in oxymonads and Paratrimastix pyriformis, suggesting specific prokaryotic donors like Firmicutes or Thermotogae.
- The downstream CIA pathway remains unaffected, implying the SUF pathway efficiently supports cytosolic and nuclear Fe-S protein maturation.
Conclusions:
- The transition from the ISC to the SUF Fe-S cluster assembly pathway is a conserved feature in Preaxostyla, preceding the loss of mitochondria in some lineages.
- The SUF pathway, potentially acquired from specific bacterial groups, successfully replaced the mitochondrial pathway without disrupting downstream processes.
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