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Published on: July 19, 2021
Distinct localization patterns of two putative mitochondrial proteins in the microsporidian Encephalitozoon cuniculi
Bryony A P Williams1, Ann Cali, Peter M Takvorian
1Department of Botany, Canadian Institute for Advanced Research, University of British Columbia, Vancouver, Canada V6T 1Z4.
Abstract:
Microsporidia were once considered amitochondriate, but have now been found to retain relict mitochondria called mitosomes. These organelles have been identified by immunolocalization in Trachipleistophora hominis, whereas most data on function have been inferred from the presence of mitochondrial protein-encoding sequences in the genome of Encephalitozoon cuniculi. Here we describe the localization of two such enzymes in E. cuniculi cells. Immunofluorescent localization of ferredoxin involved in mitochondrial iron-sulfur cluster assembly reveals a punctate distribution as expected for mitochondria. In contrast, localization of mitochondrial glycerol-3-phosphate dehydrogenase suggests a cytoplasmic distribution in E. cuniculi and possible relocalization of this typically mitochondrial protein.
Insights
Microsporidia retain relict mitochondria called mitosomes. In Encephalitozoon cuniculi, ferredoxin localizes to mitosomes, but glycerol-3-phosphate dehydrogenase appears cytoplasmic, suggesting altered function.
Area of Science:
- Cell Biology
- Parasitology
- Mitochondrial Biology
Background:
- Microsporidia were historically considered to lack mitochondria.
- Current research identifies relict mitochondria, termed mitosomes, in Microsporidia.
- Functional data on mitosomes often relies on genomic information, particularly from Encephalitozoon cuniculi.
Purpose of the Study:
- To investigate the subcellular localization of specific mitochondrial enzymes in Encephalitozoon cuniculi.
- To determine the precise location of ferredoxin and glycerol-3-phosphate dehydrogenase within E. cuniculi cells.
- To infer potential functional adaptations of mitosomes based on enzyme localization.
Main Methods:
- Immunofluorescent localization was employed to visualize specific proteins within E. cuniculi.
- Antibodies against ferredoxin and glycerol-3-phosphate dehydrogenase were used for detection.
- Cellular distribution patterns were analyzed to infer organelle localization.
Main Results:
- Ferredoxin, an enzyme crucial for iron-sulfur cluster assembly, exhibited a punctate distribution, consistent with mitochondrial localization.
- Mitochondrial glycerol-3-phosphate dehydrogenase showed a predominantly cytoplasmic distribution, deviating from its typical mitochondrial location.
- These findings suggest potential functional divergence or relocalization of enzymes within E. cuniculi mitosomes.
Conclusions:
- The study confirms the presence and mitochondrial localization of ferredoxin in E. cuniculi mitosomes.
- The cytoplasmic localization of glycerol-3-phosphate dehydrogenase indicates a possible functional specialization or mislocalization in these parasites.
- Further research is needed to fully elucidate the functional repertoire of Microsporidia mitosomes.
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