Signaling the mitochondrial unfolded protein response Journal Article


Authors: Pellegrino, M. W.; Nargund, A. M.; Haynes, C. M.
Article Title: Signaling the mitochondrial unfolded protein response
Abstract: Mitochondria are compartmentalized organelles essential for numerous cellular functions including ATP generation, iron-sulfur cluster biogenesis, nucleotide and amino acid metabolism as well as apoptosis. To promote biogenesis and proper function, mitochondria have a dedicated repertoire of molecular chaperones to facilitate protein folding and quality control proteases to degrade those proteins that fail to fold correctly. Mitochondrial protein folding is challenged by the complex organelle architecture, the deleterious effects of electron transport chain-generated reactive oxygen species and the mitochondrial genome's susceptibility to acquiring mutations. In response to the accumulation of unfolded or misfolded proteins beyond the organelle's chaperone capacity, cells mount a mitochondrial unfolded protein response (UPRmt). The UPRmt is a mitochondria-to-nuclear signal transduction pathway resulting in the induction of mitochondrial protective genes including mitochondrial molecular chaperones and proteases to re-establish protein homeostasis within the mitochondrial protein-folding environment. Here, we review the current understanding of UPRmt signal transduction and the impact of the UPRmt on diseased cells. This article is part of a Special Issue entitled: Protein Import and Quality Control in Mitochondria and Plastids. © 2012 Elsevier B.V.
Keywords: signal transduction; nonhuman; cell viability; signaling; protein degradation; cancer therapy; endoplasmic reticulum; genetic susceptibility; protein folding; homeostasis; mitochondria; mitochondrion; biogenesis; mammal cell; molecular chaperones; proteases; protein homeostasis; unfolded protein response; electron transport; membrane potential; upr; chaperonin 60; citrate synthase
Journal Title: Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Volume: 1833
Issue: 2
ISSN: 0167-4889
Publisher: Elsevier B.V.  
Date Published: 2013-02-01
Start Page: 410
End Page: 416
Language: English
DOI: 10.1016/j.bbamcr.2012.02.019
PROVIDER: scopus
PMCID: PMC3393825
PUBMED: 22445420
DOI/URL:
Notes: --- - "Export Date: 1 February 2013" - "CODEN: BAMRD" - "Source: Scopus"
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Cole Haynes
    24 Haynes
  2. Amrita Mohan Nargund
    12 Nargund