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The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond

Disulfide bond formation drives protein import of most proteins of the mitochondrial intermembrane space (IMS). The main components of this disulfide relay machinery are the oxidoreductase Mia40 and the sulfhydryl oxidase Erv1/ALR. Their precise functions have been elucidated in molecular detail for...

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Autores principales: Fischer, Manuel, Riemer, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848088/
https://www.ncbi.nlm.nih.gov/pubmed/24348563
http://dx.doi.org/10.1155/2013/742923
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author Fischer, Manuel
Riemer, Jan
author_facet Fischer, Manuel
Riemer, Jan
author_sort Fischer, Manuel
collection PubMed
description Disulfide bond formation drives protein import of most proteins of the mitochondrial intermembrane space (IMS). The main components of this disulfide relay machinery are the oxidoreductase Mia40 and the sulfhydryl oxidase Erv1/ALR. Their precise functions have been elucidated in molecular detail for the yeast and human enzymes in vitro and in intact cells. However, we still lack knowledge on how Mia40 and Erv1/ALR impact cellular and organism physiology and whether they have functions beyond their role in disulfide bond formation. Here we summarize the principles of oxidation-dependent protein import mediated by the mitochondrial disulfide relay. We proceed by discussing recently described functions of Mia40 in the hypoxia response and of ALR in influencing mitochondrial morphology and its importance for tissue development and embryogenesis. We also include a discussion of the still mysterious function of Erv1/ALR in liver regeneration.
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spelling pubmed-38480882013-12-12 The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond Fischer, Manuel Riemer, Jan Int J Cell Biol Review Article Disulfide bond formation drives protein import of most proteins of the mitochondrial intermembrane space (IMS). The main components of this disulfide relay machinery are the oxidoreductase Mia40 and the sulfhydryl oxidase Erv1/ALR. Their precise functions have been elucidated in molecular detail for the yeast and human enzymes in vitro and in intact cells. However, we still lack knowledge on how Mia40 and Erv1/ALR impact cellular and organism physiology and whether they have functions beyond their role in disulfide bond formation. Here we summarize the principles of oxidation-dependent protein import mediated by the mitochondrial disulfide relay. We proceed by discussing recently described functions of Mia40 in the hypoxia response and of ALR in influencing mitochondrial morphology and its importance for tissue development and embryogenesis. We also include a discussion of the still mysterious function of Erv1/ALR in liver regeneration. Hindawi Publishing Corporation 2013 2013-11-14 /pmc/articles/PMC3848088/ /pubmed/24348563 http://dx.doi.org/10.1155/2013/742923 Text en Copyright © 2013 M. Fischer and J. Riemer. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Fischer, Manuel
Riemer, Jan
The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title_full The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title_fullStr The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title_full_unstemmed The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title_short The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
title_sort mitochondrial disulfide relay system: roles in oxidative protein folding and beyond
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848088/
https://www.ncbi.nlm.nih.gov/pubmed/24348563
http://dx.doi.org/10.1155/2013/742923
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