Cargando…

A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress

Endoplasmic reticulum (ER) stress‐dependent accumulation of incorrectly folded proteins leads to activation of the unfolded protein response. The role of the unfolded protein response (UPR) is to avoid cell damage and restore the homeostatic state by autophagy; however, excessive ER stress results i...

Descripción completa

Detalles Bibliográficos
Autores principales: Márton, Margita, Bánhegyi, Gábor, Gyöngyösi, Norbert, Kálmán, Eszter Éva, Pettkó‐Szandtner, Aladár, Káldi, Krisztina, Kapuy, Orsolya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623533/
https://www.ncbi.nlm.nih.gov/pubmed/36097827
http://dx.doi.org/10.1002/2211-5463.13484
_version_ 1784822017907752960
author Márton, Margita
Bánhegyi, Gábor
Gyöngyösi, Norbert
Kálmán, Eszter Éva
Pettkó‐Szandtner, Aladár
Káldi, Krisztina
Kapuy, Orsolya
author_facet Márton, Margita
Bánhegyi, Gábor
Gyöngyösi, Norbert
Kálmán, Eszter Éva
Pettkó‐Szandtner, Aladár
Káldi, Krisztina
Kapuy, Orsolya
author_sort Márton, Margita
collection PubMed
description Endoplasmic reticulum (ER) stress‐dependent accumulation of incorrectly folded proteins leads to activation of the unfolded protein response. The role of the unfolded protein response (UPR) is to avoid cell damage and restore the homeostatic state by autophagy; however, excessive ER stress results in apoptosis. Here we investigated the ER stress‐dependent feedback loops inside one of the UPR branches by focusing on PERK‐induced ATF4 and its two targets, called CHOP and GADD34. Our goal was to qualitatively describe the dynamic behavior of the system by exploring the key regulatory motifs using both molecular and theoretical biological techniques. Using the HEK293T cell line as a model system, we confirmed that the life‐or‐death decision is strictly regulated. We investigated the dynamic characteristics of the crucial elements of the PERK pathway at both the RNA and protein level upon tolerable and excessive levels of ER stress. Of particular note, inhibition of GADD34 or CHOP resulted in various phenotypes upon high levels of ER stress. Our computer simulations suggest the existence of two new feedback loops inside the UPR. First, GADD34 seems to have a positive effect on ATF4 activity, while CHOP inhibits it. We claim that these newly described feedback loops ensure the fine‐tuning of the ATF4‐dependent stress response mechanism of the cell.
format Online
Article
Text
id pubmed-9623533
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-96235332022-11-02 A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress Márton, Margita Bánhegyi, Gábor Gyöngyösi, Norbert Kálmán, Eszter Éva Pettkó‐Szandtner, Aladár Káldi, Krisztina Kapuy, Orsolya FEBS Open Bio Research Articles Endoplasmic reticulum (ER) stress‐dependent accumulation of incorrectly folded proteins leads to activation of the unfolded protein response. The role of the unfolded protein response (UPR) is to avoid cell damage and restore the homeostatic state by autophagy; however, excessive ER stress results in apoptosis. Here we investigated the ER stress‐dependent feedback loops inside one of the UPR branches by focusing on PERK‐induced ATF4 and its two targets, called CHOP and GADD34. Our goal was to qualitatively describe the dynamic behavior of the system by exploring the key regulatory motifs using both molecular and theoretical biological techniques. Using the HEK293T cell line as a model system, we confirmed that the life‐or‐death decision is strictly regulated. We investigated the dynamic characteristics of the crucial elements of the PERK pathway at both the RNA and protein level upon tolerable and excessive levels of ER stress. Of particular note, inhibition of GADD34 or CHOP resulted in various phenotypes upon high levels of ER stress. Our computer simulations suggest the existence of two new feedback loops inside the UPR. First, GADD34 seems to have a positive effect on ATF4 activity, while CHOP inhibits it. We claim that these newly described feedback loops ensure the fine‐tuning of the ATF4‐dependent stress response mechanism of the cell. John Wiley and Sons Inc. 2022-09-27 /pmc/articles/PMC9623533/ /pubmed/36097827 http://dx.doi.org/10.1002/2211-5463.13484 Text en © 2022 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Márton, Margita
Bánhegyi, Gábor
Gyöngyösi, Norbert
Kálmán, Eszter Éva
Pettkó‐Szandtner, Aladár
Káldi, Krisztina
Kapuy, Orsolya
A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title_full A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title_fullStr A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title_full_unstemmed A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title_short A systems biological analysis of the ATF4‐GADD34‐CHOP regulatory triangle upon endoplasmic reticulum stress
title_sort systems biological analysis of the atf4‐gadd34‐chop regulatory triangle upon endoplasmic reticulum stress
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623533/
https://www.ncbi.nlm.nih.gov/pubmed/36097827
http://dx.doi.org/10.1002/2211-5463.13484
work_keys_str_mv AT martonmargita asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT banhegyigabor asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT gyongyosinorbert asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kalmanesztereva asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT pettkoszandtneraladar asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kaldikrisztina asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kapuyorsolya asystemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT martonmargita systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT banhegyigabor systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT gyongyosinorbert systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kalmanesztereva systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT pettkoszandtneraladar systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kaldikrisztina systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress
AT kapuyorsolya systemsbiologicalanalysisoftheatf4gadd34chopregulatorytriangleuponendoplasmicreticulumstress