Adaptation to ER stress is mediated by differential stabilities of pro-survival and pro-apoptotic mRNAs and proteins.

Bibliographic Details
Title: Adaptation to ER stress is mediated by differential stabilities of pro-survival and pro-apoptotic mRNAs and proteins.
Authors: D Thomas Rutkowski, Stacey M Arnold, Corey N Miller, Jun Wu, Jack Li, Kathryn M Gunnison, Kazutoshi Mori, Amir A Sadighi Akha, David Raden, Randal J Kaufman
Source: PLoS Biology, Vol 4, Iss 11, p e374 (2006)
Publisher Information: Public Library of Science (PLoS), 2006.
Publication Year: 2006
Collection: LCC:Biology (General)
Subject Terms: Biology (General), QH301-705.5
More Details: The accumulation of unfolded proteins in the endoplasmic reticulum (ER) activates a signaling cascade known as the unfolded protein response (UPR). Although activation of the UPR is well described, there is little sense of how the response, which initiates both apoptotic and adaptive pathways, can selectively allow for adaptation. Here we describe the reconstitution of an adaptive ER stress response in a cell culture system. Monitoring the activation and maintenance of representative UPR gene expression pathways that facilitate either adaptation or apoptosis, we demonstrate that mild ER stress activates all UPR sensors. However, survival is favored during mild stress as a consequence of the intrinsic instabilities of mRNAs and proteins that promote apoptosis compared to those that facilitate protein folding and adaptation. As a consequence, the expression of apoptotic proteins is short-lived as cells adapt to stress. We provide evidence that the selective persistence of ER chaperone expression is also applicable to at least one instance of genetic ER stress. This work provides new insight into how a stress response pathway can be structured to allow cells to avert death as they adapt. It underscores the contribution of posttranscriptional and posttranslational mechanisms in influencing this outcome.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1544-9173
1545-7885
Relation: http://europepmc.org/articles/PMC1634883?pdf=render; https://doaj.org/toc/1544-9173; https://doaj.org/toc/1545-7885
DOI: 10.1371/journal.pbio.0040374
Access URL: https://doaj.org/article/a026c3ed14ba4c9a93f5af077eeaf9c4
Accession Number: edsdoj.026c3ed14ba4c9a93f5af077eeaf9c4
Database: Directory of Open Access Journals
More Details
ISSN:15449173
15457885
DOI:10.1371/journal.pbio.0040374
Published in:PLoS Biology
Language:English