https://wiki.oroboros.at/index.php?title=Fessler_2020_Nature&feed=atom&action=historyFessler 2020 Nature - Revision history2024-03-29T13:17:10ZRevision history for this page on the wikiMediaWiki 1.36.1https://wiki.oroboros.at/index.php?title=Fessler_2020_Nature&diff=219627&oldid=prevKomlodi Timea at 07:07, 16 August 20212021-08-16T07:07:07Z<p></p>
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</table>Komlodi Timeahttps://wiki.oroboros.at/index.php?title=Fessler_2020_Nature&diff=216240&oldid=prevKomlodi Timea at 10:48, 15 March 20212021-03-15T10:48:11Z<p></p>
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</table>Komlodi Timeahttps://wiki.oroboros.at/index.php?title=Fessler_2020_Nature&diff=216224&oldid=prevKomlodi Timea: Created page with "{{Publication |title=Fessler E, Eckl EM, Schmitt S, Mancilla IA, Meyer-Bender MF, Hanf M, Philippou-Massier J, Krebs S, Zischka H, Jae LT (2020) A pathway coordinated by DELE1..."2021-03-15T09:47:09Z<p>Created page with "{{Publication |title=Fessler E, Eckl EM, Schmitt S, Mancilla IA, Meyer-Bender MF, Hanf M, Philippou-Massier J, Krebs S, Zischka H, Jae LT (2020) A pathway coordinated by DELE1..."</p>
<p><b>New page</b></p><div>{{Publication<br />
|title=Fessler E, Eckl EM, Schmitt S, Mancilla IA, Meyer-Bender MF, Hanf M, Philippou-Massier J, Krebs S, Zischka H, Jae LT (2020) A pathway coordinated by DELE1 relays mitochondrial stress to the cytosol.. Nature 579:433-437.<br />
|info=[https://pubmed.ncbi.nlm.nih.gov/32132706/ PMID:32132706 Open Access]<br />
|authors=Fessler E, Eckl EM, Schmitt S, Mancilla IA, Meyer-Bender MF, Hanf M, Philippou-Massier J, Krebs S, Zischka H, Jae LT<br />
|year=2020<br />
|journal=Nature<br />
|abstract=Mitochondrial fidelity is tightly linked to overall cellular homeostasis and is compromised in ageing and various pathologies1-3. Mitochondrial malfunction needs to be relayed to the cytosol, where an integrated stress response is triggered by the phosphorylation of eukaryotic translation initiation factor 2α (eIF2α) in mammalian cells4,5. eIF2α phosphorylation is mediated by the four eIF2α kinases GCN2, HRI, PERK and PKR, which are activated by diverse types of cellular stress6. However, the machinery that communicates mitochondrial perturbation to the cytosol to trigger the integrated stress response remains unknown1,2,7. Here we combine genome engineering and haploid genetics to unbiasedly identify genes that affect the induction of C/EBP homologous protein (CHOP), a key factor in the integrated stress response. We show that the mitochondrial protease OMA1 and the poorly characterized protein DELE1, together with HRI, constitute the missing pathway that is triggered by mitochondrial stress. Mechanistically, stress-induced activation of OMA1 causes DELE1 to be cleaved into a short form that accumulates in the cytosol, where it binds to and activates HRI via its C-terminal portion. Obstruction of this pathway can be beneficial or adverse depending on the type of mitochondrial perturbation. In addition to the core pathway components, our comparative genetic screening strategy identifies a suite of additional regulators. Together, these findings could be used to inform future strategies to modulate the cellular response to mitochondrial dysfunction in the context of human disease.<br />
}}<br />
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