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Temporal landscape of mitochondrial proteostasis governed by the UPRmt

Breakdown of mitochondrial proteostasis activates quality control pathways including the mitochondrial unfolded protein response (UPRmt) and PINK1/Parkin mitophagy. However, beyond the up-regulation of chaperones and proteases, we have a limited understanding of how the UPRmt remodels and restores damaged mitochondrial proteomes. Here, we have developed a functional proteomics framework, termed MitoPQ (Mitochondrial Proteostasis Quantification), to dissect the UPRmt's role in maintaining proteostasis during stress. We find essential roles for the UPRmt in both protecting and repairing proteostasis, with oxidative phosphorylation metabolism being a central target of the UPRmt. Transcriptome analyses together with MitoPQ reveal that UPRmt transcription factors drive independent signaling arms that act in concert to maintain proteostasis. Unidirectional interplay between the UPRmt and PINK1/Parkin mitophagy was found to promote oxidative phosphorylation recovery when the UPRmt failed. Collectively, this study defines the network of proteostasis mediated by the UPRmt and highlights the value of functional proteomics in decoding stressed proteomes.

 

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This passage dives deep into the realm of mitochondrial biology and proteostasis, focusing on the mechanisms involved in maintaining and repairing damaged mitochondrial proteins during stress. Here's a breakdown:

1. **Mitochondrial Proteostasis and Stress Response:** Mitochondria, crucial for cellular energy production, face stress and damage. To counteract this, cells activate pathways like the mitochondrial unfolded protein response (UPRmt) and PINK1/Parkin-mediated mitophagy.

2. **Limitations in Understanding UPRmt:** While we know that UPRmt triggers the upregulation of chaperones and proteases to tackle stress, understanding its precise remodeling and restoration of damaged mitochondrial proteins is limited.

3. **Development of MitoPQ:** The authors introduce a new method, MitoPQ (Mitochondrial Proteostasis Quantification), a functional proteomics framework. This tool aims to dissect and quantify UPRmt's role in maintaining proteostasis during stress.

4. **UPRmt's Role in Proteostasis:** The study reveals that UPRmt plays a significant role in both protecting and repairing mitochondrial proteostasis. It specifically targets oxidative phosphorylation metabolism, a central component of mitochondrial function.

5. **Transcriptome Analysis and UPRmt:** By analyzing gene expression patterns (transcriptome analyses) alongside MitoPQ, the study identifies that UPRmt-driven transcription factors orchestrate independent signaling pathways that work together to maintain proteostasis.

6. **UPRmt and PINK1/Parkin Mitophagy:** The interaction between UPRmt and PINK1/Parkin-mediated mitophagy is highlighted. This interaction fosters oxidative phosphorylation recovery when UPRmt functions inadequately.

7. **Concluding Insights:** The study defines the network of proteostasis controlled by UPRmt and emphasizes the importance of functional proteomics in understanding stressed proteomes.

Overall, this research offers a comprehensive view of how UPRmt intervenes in managing mitochondrial proteostasis during stress, shedding light on the intricate pathways and mechanisms involved.

Related Products

Cat.No. Product Name Information
E1252 MitoPQ MitoPQ (MitoParaquat), a mitochondria-targeted redox cycler, enables the selective generation of superoxide within mitochondria and is a useful tool to investigate the many roles of mitochondrial superoxide in pathology and redox signaling in cells and in vivo.

Related Targets

Mitochondrial Metabolism