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Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals

Mitochondrial stress activates a mitonuclear response to safeguard and repair mitochondrial function and to adapt cellular metabolism to stress. Using a multiomics approach in mammalian cells treated with four types of mitochondrial stressors, we identify activating transcription factor 4 (ATF4) as...

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Autores principales: Quirós, Pedro M., Prado, Miguel A., Zamboni, Nicola, D’Amico, Davide, Williams, Robert W., Finley, Daniel, Gygi, Steven P., Auwerx, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496626/
https://www.ncbi.nlm.nih.gov/pubmed/28566324
http://dx.doi.org/10.1083/jcb.201702058
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author Quirós, Pedro M.
Prado, Miguel A.
Zamboni, Nicola
D’Amico, Davide
Williams, Robert W.
Finley, Daniel
Gygi, Steven P.
Auwerx, Johan
author_facet Quirós, Pedro M.
Prado, Miguel A.
Zamboni, Nicola
D’Amico, Davide
Williams, Robert W.
Finley, Daniel
Gygi, Steven P.
Auwerx, Johan
author_sort Quirós, Pedro M.
collection PubMed
description Mitochondrial stress activates a mitonuclear response to safeguard and repair mitochondrial function and to adapt cellular metabolism to stress. Using a multiomics approach in mammalian cells treated with four types of mitochondrial stressors, we identify activating transcription factor 4 (ATF4) as the main regulator of the stress response. Surprisingly, canonical mitochondrial unfolded protein response genes mediated by ATF5 are not activated. Instead, ATF4 activates the expression of cytoprotective genes, which reprogram cellular metabolism through activation of the integrated stress response (ISR). Mitochondrial stress promotes a local proteostatic response by reducing mitochondrial ribosomal proteins, inhibiting mitochondrial translation, and coupling the activation of the ISR with the attenuation of mitochondrial function. Through a trans–expression quantitative trait locus analysis, we provide genetic evidence supporting a role for Fh1 in the control of Atf4 expression in mammals. Using gene expression data from mice and humans with mitochondrial diseases, we show that the ATF4 pathway is activated in vivo upon mitochondrial stress. Our data illustrate the value of a multiomics approach to characterize complex cellular networks and provide a versatile resource to identify new regulators of mitochondrial-related diseases.
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spelling pubmed-54966262018-01-03 Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals Quirós, Pedro M. Prado, Miguel A. Zamboni, Nicola D’Amico, Davide Williams, Robert W. Finley, Daniel Gygi, Steven P. Auwerx, Johan J Cell Biol Research Articles Mitochondrial stress activates a mitonuclear response to safeguard and repair mitochondrial function and to adapt cellular metabolism to stress. Using a multiomics approach in mammalian cells treated with four types of mitochondrial stressors, we identify activating transcription factor 4 (ATF4) as the main regulator of the stress response. Surprisingly, canonical mitochondrial unfolded protein response genes mediated by ATF5 are not activated. Instead, ATF4 activates the expression of cytoprotective genes, which reprogram cellular metabolism through activation of the integrated stress response (ISR). Mitochondrial stress promotes a local proteostatic response by reducing mitochondrial ribosomal proteins, inhibiting mitochondrial translation, and coupling the activation of the ISR with the attenuation of mitochondrial function. Through a trans–expression quantitative trait locus analysis, we provide genetic evidence supporting a role for Fh1 in the control of Atf4 expression in mammals. Using gene expression data from mice and humans with mitochondrial diseases, we show that the ATF4 pathway is activated in vivo upon mitochondrial stress. Our data illustrate the value of a multiomics approach to characterize complex cellular networks and provide a versatile resource to identify new regulators of mitochondrial-related diseases. The Rockefeller University Press 2017-07-03 /pmc/articles/PMC5496626/ /pubmed/28566324 http://dx.doi.org/10.1083/jcb.201702058 Text en © 2017 Quirós et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Quirós, Pedro M.
Prado, Miguel A.
Zamboni, Nicola
D’Amico, Davide
Williams, Robert W.
Finley, Daniel
Gygi, Steven P.
Auwerx, Johan
Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title_full Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title_fullStr Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title_full_unstemmed Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title_short Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
title_sort multi-omics analysis identifies atf4 as a key regulator of the mitochondrial stress response in mammals
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496626/
https://www.ncbi.nlm.nih.gov/pubmed/28566324
http://dx.doi.org/10.1083/jcb.201702058
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