Crosstalk between cellular compartments protects against proteotoxicity and extends lifespan

In cells living under optimal conditions, protein folding defects are usually prevented by the action of chaperones. Here, we investigate the cell-wide consequences of loss of chaperone function in cytosol, mitochondria or the endoplasmic reticulum (ER) in budding yeast. We find that the decline in...

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Bibliographic Details
Published in:Scientific reports 2016-06, Vol.6 (1), p.28751-28751, Article 28751
Main Authors: Perić, Matea, Bou Dib, Peter, Dennerlein, Sven, Musa, Marina, Rudan, Marina, Lovrić, Anita, Nikolić, Andrea, Šarić, Ana, Sobočanec, Sandra, Mačak, Željka, Raimundo, Nuno, Kriško, Anita
Format: Article
Language:English
Subjects:
Endoplasmic reticulum
Homeostasis
Metabolism
Mitochondria
Protein folding
Respiration
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Summary:In cells living under optimal conditions, protein folding defects are usually prevented by the action of chaperones. Here, we investigate the cell-wide consequences of loss of chaperone function in cytosol, mitochondria or the endoplasmic reticulum (ER) in budding yeast. We find that the decline in chaperone activity in each compartment results in loss of respiration, demonstrating the dependence of mitochondrial activity on cell-wide proteostasis. Furthermore, each chaperone deficiency triggers a response, presumably via the communication among the folding environments of distinct cellular compartments, termed here the cross-organelle stress response (CORE). The proposed CORE pathway encompasses activation of protein conformational maintenance machineries, antioxidant enzymes, and metabolic changes simultaneously in the cytosol, mitochondria, and the ER. CORE induction extends replicative and chronological lifespan in budding yeast, highlighting its protective role against moderate proteotoxicity and its consequences such as the decline in respiration. Our findings accentuate that organelles do not function in isolation, but are integrated in a functional crosstalk, while also highlighting the importance of organelle communication in aging and age-related diseases.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep28751