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Updated: Jun 27, 2026

Measurement of Protein Import Capacity of Skeletal Muscle Mitochondria
Published on: January 7, 2022
Evidence of a reduced and modified mitochondrial protein import apparatus in microsporidian mitosomes
Ross F Waller1, Carole Jabbour, Nickie C Chan
1School of Botany, University of Melbourne, Victoria, Australia. r.waller@unimelb.edu.au
Abstract:
Microsporidia are a group of highly adapted obligate intracellular parasites that are now recognized as close relatives of fungi. Their adaptation to parasitism has resulted in broad and severe reduction at (i) a genomic level by extensive gene loss, gene compaction, and gene shortening; (ii) a biochemical level with the loss of much basic metabolism; and (iii) a cellular level, resulting in lost or cryptic organelles. Consistent with this trend, the mitochondrion is severely reduced, lacking ATP synthesis and other typical functions and apparently containing only a fraction of the proteins of canonical mitochondria. We have investigated the mitochondrial protein import apparatus of this reduced organelle in the microsporidian Encephalitozoon cuniculi and find evidence of reduced and modified machinery. Notably, a putative outer membrane receptor, Tom70, is reduced in length but maintains a conserved structure chiefly consisting of tetratricopeptide repeats. When expressed in Saccharomyces cerevisiae, EcTom70 inserts with the correct topology into the outer membrane of mitochondria but is unable to complement the growth defects of Tom70-deficient yeast. We have scanned genomic data using hidden Markov models for other homologues of import machinery proteins and find evidence of severe reduction of this system.
Insights
Microsporidia have highly reduced mitochondria with a simplified protein import system. Researchers found a shortened Tom70 protein in Encephalitozoon cuniculi, indicating significant evolutionary adaptation.
Area of Science:
- Mycology
- Parasitology
- Cell Biology
Background:
- Microsporidia are obligate intracellular parasites closely related to fungi.
- Parasitism has driven extreme genomic, biochemical, and cellular reductions in microsporidia.
- Mitochondria in microsporidia are severely reduced, lacking typical functions like ATP synthesis.
Purpose of the Study:
- To investigate the mitochondrial protein import apparatus in the microsporidian Encephalitozoon cuniculi.
- To characterize the function of a reduced outer membrane receptor, Tom70, in microsporidian mitochondria.
Main Methods:
- Genomic data analysis using hidden Markov models to identify import machinery proteins.
- Expression of the Encephalitozoon cuniculi Tom70 (EcTom70) in Saccharomyces cerevisiae.
- Analysis of EcTom70 topology and function in yeast mitochondria.
Main Results:
- Evidence of a reduced and modified mitochondrial protein import machinery in Encephalitozoon cuniculi.
- A putative outer membrane receptor, Tom70, is shortened but retains conserved structural features (tetratricopeptide repeats).
- EcTom70 correctly inserts into yeast mitochondria but cannot rescue growth defects in Tom70-deficient yeast, suggesting functional limitations.
Conclusions:
- The mitochondrial protein import system in microsporidia is significantly reduced and modified, consistent with their parasitic lifestyle.
- The functional capacity of microsporidian mitochondria, including protein import, is severely compromised.
- Further genomic scanning revealed a broader reduction in the mitochondrial import machinery system.
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