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Physiological/pathological ramifications of transcription factors in the unfolded protein response

Numerous environmental, physiological, and pathological insults disrupt protein-folding homeostasis in the endoplasmic reticulum (ER), referred to as ER stress. Eukaryotic cells evolved a set of intracellular signaling pathways, collectively termed the unfolded protein response (UPR), to maintain a...

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Detalles Bibliográficos
Autores principales: Han, Jaeseok, Kaufman, Randal J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588925/
https://www.ncbi.nlm.nih.gov/pubmed/28860159
http://dx.doi.org/10.1101/gad.297374.117
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author Han, Jaeseok
Kaufman, Randal J.
author_facet Han, Jaeseok
Kaufman, Randal J.
author_sort Han, Jaeseok
collection PubMed
description Numerous environmental, physiological, and pathological insults disrupt protein-folding homeostasis in the endoplasmic reticulum (ER), referred to as ER stress. Eukaryotic cells evolved a set of intracellular signaling pathways, collectively termed the unfolded protein response (UPR), to maintain a productive ER protein-folding environment through reprogramming gene transcription and mRNA translation. The UPR is largely dependent on transcription factors (TFs) that modulate expression of genes involved in many physiological and pathological conditions, including development, metabolism, inflammation, neurodegenerative diseases, and cancer. Here we summarize the current knowledge about these mechanisms, their impact on physiological/pathological processes, and potential therapeutic applications.
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spelling pubmed-55889252017-09-21 Physiological/pathological ramifications of transcription factors in the unfolded protein response Han, Jaeseok Kaufman, Randal J. Genes Dev Review Numerous environmental, physiological, and pathological insults disrupt protein-folding homeostasis in the endoplasmic reticulum (ER), referred to as ER stress. Eukaryotic cells evolved a set of intracellular signaling pathways, collectively termed the unfolded protein response (UPR), to maintain a productive ER protein-folding environment through reprogramming gene transcription and mRNA translation. The UPR is largely dependent on transcription factors (TFs) that modulate expression of genes involved in many physiological and pathological conditions, including development, metabolism, inflammation, neurodegenerative diseases, and cancer. Here we summarize the current knowledge about these mechanisms, their impact on physiological/pathological processes, and potential therapeutic applications. Cold Spring Harbor Laboratory Press 2017-07-15 /pmc/articles/PMC5588925/ /pubmed/28860159 http://dx.doi.org/10.1101/gad.297374.117 Text en © 2017 Han and Kaufman; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Han, Jaeseok
Kaufman, Randal J.
Physiological/pathological ramifications of transcription factors in the unfolded protein response
title Physiological/pathological ramifications of transcription factors in the unfolded protein response
title_full Physiological/pathological ramifications of transcription factors in the unfolded protein response
title_fullStr Physiological/pathological ramifications of transcription factors in the unfolded protein response
title_full_unstemmed Physiological/pathological ramifications of transcription factors in the unfolded protein response
title_short Physiological/pathological ramifications of transcription factors in the unfolded protein response
title_sort physiological/pathological ramifications of transcription factors in the unfolded protein response
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588925/
https://www.ncbi.nlm.nih.gov/pubmed/28860159
http://dx.doi.org/10.1101/gad.297374.117
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