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IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans

BACKGROUND: The General Control Nonderepressible 2 (GCN2) kinase is a conserved member of the integrated stress response (ISR) pathway that represses protein translation and helps cells to adapt to conditions of nutrient shortage. As such, GCN2 is required for longevity and stress resistance induced...

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Autores principales: Ferraz, Rafael C., Camara, Henrique, De-Souza, Evandro A., Pinto, Silas, Pinca, Ana Paula F., Silva, Richard C., Sato, Vitor N., Castilho, Beatriz A., Mori, Marcelo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054600/
https://www.ncbi.nlm.nih.gov/pubmed/27717342
http://dx.doi.org/10.1186/s12915-016-0301-2
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author Ferraz, Rafael C.
Camara, Henrique
De-Souza, Evandro A.
Pinto, Silas
Pinca, Ana Paula F.
Silva, Richard C.
Sato, Vitor N.
Castilho, Beatriz A.
Mori, Marcelo A.
author_facet Ferraz, Rafael C.
Camara, Henrique
De-Souza, Evandro A.
Pinto, Silas
Pinca, Ana Paula F.
Silva, Richard C.
Sato, Vitor N.
Castilho, Beatriz A.
Mori, Marcelo A.
author_sort Ferraz, Rafael C.
collection PubMed
description BACKGROUND: The General Control Nonderepressible 2 (GCN2) kinase is a conserved member of the integrated stress response (ISR) pathway that represses protein translation and helps cells to adapt to conditions of nutrient shortage. As such, GCN2 is required for longevity and stress resistance induced by dietary restriction (DR). IMPACT is an ancient protein that inhibits GCN2. RESULTS: Here, we tested whether IMPACT down-regulation mimics the effects of DR in C. elegans. Knockdown of the C. elegans IMPACT homolog impt-1 activated the ISR pathway and increased lifespan and stress resistance of worms in a gcn-2-dependent manner. Impt-1 knockdown exacerbated DR-induced longevity and required several DR-activated transcription factors to extend lifespan, among them SKN-1 and DAF-16, which were induced during larval development and adulthood, respectively, in response to impt-1 RNAi. CONCLUSIONS: IMPACT inhibits the ISR pathway, thus limiting the activation of stress response factors that are beneficial during aging and required under DR. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0301-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-50546002016-10-19 IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans Ferraz, Rafael C. Camara, Henrique De-Souza, Evandro A. Pinto, Silas Pinca, Ana Paula F. Silva, Richard C. Sato, Vitor N. Castilho, Beatriz A. Mori, Marcelo A. BMC Biol Research Article BACKGROUND: The General Control Nonderepressible 2 (GCN2) kinase is a conserved member of the integrated stress response (ISR) pathway that represses protein translation and helps cells to adapt to conditions of nutrient shortage. As such, GCN2 is required for longevity and stress resistance induced by dietary restriction (DR). IMPACT is an ancient protein that inhibits GCN2. RESULTS: Here, we tested whether IMPACT down-regulation mimics the effects of DR in C. elegans. Knockdown of the C. elegans IMPACT homolog impt-1 activated the ISR pathway and increased lifespan and stress resistance of worms in a gcn-2-dependent manner. Impt-1 knockdown exacerbated DR-induced longevity and required several DR-activated transcription factors to extend lifespan, among them SKN-1 and DAF-16, which were induced during larval development and adulthood, respectively, in response to impt-1 RNAi. CONCLUSIONS: IMPACT inhibits the ISR pathway, thus limiting the activation of stress response factors that are beneficial during aging and required under DR. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0301-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-07 /pmc/articles/PMC5054600/ /pubmed/27717342 http://dx.doi.org/10.1186/s12915-016-0301-2 Text en © Ferraz et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ferraz, Rafael C.
Camara, Henrique
De-Souza, Evandro A.
Pinto, Silas
Pinca, Ana Paula F.
Silva, Richard C.
Sato, Vitor N.
Castilho, Beatriz A.
Mori, Marcelo A.
IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title_full IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title_fullStr IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title_full_unstemmed IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title_short IMPACT is a GCN2 inhibitor that limits lifespan in Caenorhabditis elegans
title_sort impact is a gcn2 inhibitor that limits lifespan in caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054600/
https://www.ncbi.nlm.nih.gov/pubmed/27717342
http://dx.doi.org/10.1186/s12915-016-0301-2
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