Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782458631896170496 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5054600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ferrazrafaelc impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT camarahenrique impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT desouzaevandroa impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT pintosilas impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT pincaanapaulaf impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT silvarichardc impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT satovitorn impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT castilhobeatriza impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans AT morimarceloa impactisagcn2inhibitorthatlimitslifespanincaenorhabditiselegans |