Article (Scientific journals)
AIF meets the CHCHD4/Mia40-dependent mitochondrial import pathway.
Reinhardt, Camille; Arena, Giuseppe; Nedara, Kenza et al.
2020In Biochimica et Biophysica Acta - Molecular Basis of Disease, 1866 (6), p. 165746
Peer Reviewed verified by ORBi
 

Files


Full Text
Reinhardt et al.pdf
Publisher postprint (914.52 kB)
Download

All documents in ORBilu are protected by a user license.

Send to



Details



Keywords :
Apoptosis Inducing Factor/genetics/metabolism; Cysteine/genetics/metabolism; Disulfides/metabolism; Electron Transport Complex I/genetics/metabolism; Gene Expression Regulation; Humans; Mitochondria/genetics/metabolism; Mitochondrial Membrane Transport Proteins/genetics; Mitochondrial Precursor Protein Import Complex Proteins; Mitochondrial Proteins/genetics; Mutation/genetics; Protein Transport/genetics; Saccharomyces cerevisiae/genetics/metabolism; Disulfide relay system; Metabolism; Mitochondria; Mitochondrial protein import; Respiratory chain machinery
Abstract :
[en] In the mitochondria of healthy cells, Apoptosis-Inducing factor (AIF) is required for the optimal functioning of the respiratory chain machinery, mitochondrial integrity, cell survival, and proliferation. In all analysed species, it was revealed that the downregulation or depletion of AIF provokes mainly the post-transcriptional loss of respiratory chain Complex I protein subunits. Recent progress in the field has revealed that AIF fulfils its mitochondrial pro-survival function by interacting physically and functionally with CHCHD4, the evolutionarily-conserved human homolog of yeast Mia40. The redox-regulated CHCHD4/Mia40-dependent import machinery operates in the intermembrane space of the mitochondrion and controls the import of a set of nuclear-encoded cysteine-motif carrying protein substrates. In addition to their participation in the biogenesis of specific respiratory chain protein subunits, CHCHD4/Mia40 substrates are also implicated in the control of redox regulation, antioxidant response, translation, lipid homeostasis and mitochondrial ultrastructure and dynamics. Here, we discuss recent insights on the AIF/CHCHD4-dependent protein import pathway and review current data concerning the CHCHD4/Mia40 protein substrates in metazoan. Recent findings and the identification of disease-associated mutations in AIF or in specific CHCHD4/Mia40 substrates have highlighted these proteins as potential therapeutic targets in a variety of human disorders.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Reinhardt, Camille
Arena, Giuseppe  ;  Université Paris-Saclay, Institut Gustave Roussy, Inserm, Radiothérapie Moléculaire, 94805 Villejuif, France.
Nedara, Kenza
Edwards, Ruairidh
Brenner, Catherine
Tokatlidis, Kostas
Modjtahedi, Nazanine
External co-authors :
yes
Language :
English
Title :
AIF meets the CHCHD4/Mia40-dependent mitochondrial import pathway.
Publication date :
2020
Journal title :
Biochimica et Biophysica Acta - Molecular Basis of Disease
ISSN :
0925-4439
Publisher :
Elsevier, Netherlands
Volume :
1866
Issue :
6
Pages :
165746
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.
Available on ORBilu :
since 05 April 2023

Statistics


Number of views
21 (0 by Unilu)
Number of downloads
9 (0 by Unilu)

Scopus citations®
 
32
Scopus citations®
without self-citations
27
OpenCitations
 
26
WoS citations
 
30

Bibliography


Similar publications



Contact ORBilu