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Updated: Apr 19, 2026

Measurement of Protein Import Capacity of Skeletal Muscle Mitochondria
Published on: January 7, 2022
OM14 is a mitochondrial receptor for cytosolic ribosomes that supports co-translational import into mitochondria
Chen Lesnik1, Yifat Cohen2, Avigail Atir-Lande1
1Department of Biology, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
Abstract:
It is well established that import of proteins into mitochondria can occur after their complete synthesis by cytosolic ribosomes. Recently, an additional model was revived, proposing that some proteins are imported co-translationally. This model entails association of ribosomes with the mitochondrial outer membrane, shown to be mediated through the ribosome-associated chaperone nascent chain-associated complex (NAC). However, the mitochondrial receptor of this complex is unknown. Here, we identify the Saccharomyces cerevisiae outer membrane protein OM14 as a receptor for NAC. OM14Δ mitochondria have significantly lower amounts of associated NAC and ribosomes, and ribosomes from NAC[Δ] cells have reduced levels of associated OM14. Importantly, mitochondrial import assays reveal a significant decrease in import efficiency into OM14Δ mitochondria, and OM14-dependent import necessitates NAC. Our results identify OM14 as the first mitochondrial receptor for ribosome-associated NAC and reveal its importance for import. These results provide a strong support for an additional, co-translational mode of import into mitochondria.
Insights
Researchers identified OM14 as the mitochondrial receptor for the nascent chain-associated complex (NAC), supporting co-translational protein import into mitochondria. This discovery highlights OM14's crucial role in mitochondrial protein targeting.
Area of Science:
- Mitochondrial biology
- Molecular cell biology
- Protein import mechanisms
Background:
- Mitochondrial protein import is essential for cellular function.
- Traditionally, proteins are imported post-translationally after cytosolic synthesis.
- A co-translational import model, involving ribosome association with mitochondria, has been proposed but lacked key receptor identification.
Purpose of the Study:
- To identify the mitochondrial receptor for the ribosome-associated chaperone, nascent chain-associated complex (NAC).
- To investigate the role of this receptor in co-translational mitochondrial protein import.
Main Methods:
- Genetic deletion analysis of the Saccharomyces cerevisiae outer membrane protein OM14.
- Biochemical assays to quantify NAC and ribosome association with mitochondria.
- Mitochondrial import assays to measure protein import efficiency.
Main Results:
- Mitochondria lacking OM14 (OM14Δ) showed reduced association of NAC and ribosomes.
- Ribosomes from NAC-deficient cells exhibited decreased OM14 association.
- Import assays demonstrated significantly reduced protein import into OM14Δ mitochondria.
- OM14-dependent import was shown to require NAC.
Conclusions:
- OM14 is identified as the first mitochondrial outer membrane receptor for ribosome-associated NAC.
- OM14 plays a critical role in facilitating co-translational protein import into mitochondria.
- These findings provide strong support for the co-translational import model into mitochondria.
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