Literature DB >> 30617048

Signaling and Regulation of the Mitochondrial Unfolded Protein Response.

Nandhitha Uma Naresh1, Cole M Haynes1.   

Abstract

The mitochondrial proteome encompasses more than a thousand proteins, which are encoded by the mitochondrial and nuclear genomes. Mitochondrial biogenesis and network health relies on maintenance of protein import pathways and the protein-folding environment. Cell-extrinsic or -intrinsic stressors that challenge mitochondrial proteostasis negatively affect organellar function. During conditions of stress, cells use impaired protein import as a sensor for mitochondrial dysfunction to activate a stress response called the mitochondrial unfolded protein response (UPRmt). UPRmt activation leads to an adaptive transcriptional program that promotes mitochondrial recovery, metabolic adaptations, and innate immunity. In this review, we discuss the regulation of UPRmt activation as well as its role in maintaining mitochondrial homeostasis in physiological and pathological scenarios.
Copyright © 2019 Cold Spring Harbor Laboratory Press; all rights reserved.

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Year:  2019        PMID: 30617048      PMCID: PMC6546047          DOI: 10.1101/cshperspect.a033944

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  125 in total

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  32 in total

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Review 6.  Functional Modules of the Proteostasis Network.

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Review 8.  Mitochondrial function in development and disease.

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10.  Effect of the mitochondrial unfolded protein response on hypoxic death and mitochondrial protein aggregation.

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