The The TOB/SAM complex composition in mitochondria of Dictyostelium discoideum during progression from unicellularity to multicellularity
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Updated: Jan 4, 2026

Author Spotlight: Unveiling Oxidative Phosphorylation System Dynamics and Mitochondrial Roles in Health and Disease
Published on: May 3, 2024
Monika Mazur1, Małgorzata Wojtkowska1, Marcin Skalski1
1Institute of Molecular Biology and Biotechnology, Department of Bioenergetics, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.
Abstract:
Despite its complex life cycle including unicellular and multicellular stages, the slime mold Dictyostelium discoideum, a well-known model in biomedical research, has not been used as a model organism in studies on mitochondrial import, including its significance in cellular processes. Moreover, data concerning mitochondrial protein import machinery in D. discoideum mitochondria is limited and nothing is known about the impact of that machinery on slime mold life cycle. Here, we focused on the TOB/SAM (topogenesis of the mitochondrial outer membrane β-barrel proteins/sorting and assembly machinery) complex. This complex is localized in the mitochondrial outer membrane and is indispensable for the formation of metabolite exchange and protein import pathways in the membrane, and substantially contributes to the regulation of mitochondrial morphology and distribution. Furthermore, the available data suggests that the TOB/SAM complex variants differ between mitochondria of multicellular and unicellular eukaryotes. Therefore, we decided to determine these variants of the TOB/SAM in mitochondria of D. discoideum progressing from single cells to early multicellular stages, when the cells stream together to form a multicellular organism. The results revealed two complex variants of the TOB/SAM complex of about 160 and 600 kDa molecular weight, present in mitochondria of D. discoideum cells at the studied stages. The discussed complex variants resemble the ones that have been already detected for the yeast Saccharomyces cerevisiae, fungus Neurospora crassa and human cells, and one of investigated variants differentiates unicellular and initial multicellular stages of the D. discoideum life cycle.
Insights
The slime mold Dictyostelium discoideum
Area of Science:
- Mitochondrial biology
- Cellular and molecular biology
- Biochemistry
Background:
- The slime mold Dictyostelium discoideum is a model organism in biomedical research.
- Mitochondrial protein import machinery in D. discoideum is understudied.
- The TOB/SAM complex is crucial for mitochondrial outer membrane protein assembly.
Purpose of the Study:
- To investigate the TOB/SAM complex variants in Dictyostelium discoideum mitochondria.
- To analyze changes in the TOB/SAM complex during the transition from unicellular to multicellular stages.
- To understand the role of the TOB/SAM complex in slime mold mitochondrial function.
Main Methods:
- Biochemical analysis of mitochondrial protein complexes.
- Size exclusion chromatography and Western blotting.
- Comparative analysis of TOB/SAM complex variants.
Main Results:
- Two TOB/SAM complex variants (160 kDa and 600 kDa) were identified in D. discoideum mitochondria.
- These variants are conserved across different eukaryotic organisms.
- One TOB/SAM variant distinguishes unicellular from early multicellular stages in D. discoideum.
Conclusions:
- Dictyostelium discoideum possesses conserved TOB/SAM complex variants.
- The TOB/SAM complex plays a role in regulating mitochondrial function during slime mold development.
- Further research can utilize D. discoideum to study mitochondrial protein import.
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