Apoptosis-inducing factor (AIF) is a mitochondrial flavoprotein that, beyond its apoptotic function, is required for the normal expression of major respiratory chain complexes. Here we identified an AIF-interacting protein, CHCHD4, which is the central component of a redox-sensitive mitochondrial intermembrane space import machinery. Depletion or hypomorphic mutation of AIF caused a downregulation of CHCHD4 protein by diminishing its mitochondrial import. CHCHD4 depletion sufficed to induce a respiratory defect that mimicked that observed in AIF-deficient cells. CHCHD4 levels could be restored in AIF-deficient cells by enforcing its AIF-independent mitochondrial localization. This modified CHCHD4 protein reestablished respiratory function in AIF-deficient cells and enabled AIF-deficient embryoid bodies to undergo cavitation, a process of programmed cell death required for embryonic morphogenesis. These findings explain how AIF contributes to the biogenesis of respiratory chain complexes, and they establish an unexpected link between the vital function of AIF and the propensity of cells to undergo apoptosis.

Hangen, E., Feraud, O., Lachkar, S., Mou, H., Doti, N., Fimia, G.m., et al. (2015). Interaction between AIF and CHCHD4 Regulates Respiratory Chain Biogenesis. MOLECULAR CELL, 58(6), 1001-1014 [10.1016/j.molcel.2015.04.020].

Interaction between AIF and CHCHD4 Regulates Respiratory Chain Biogenesis

Piacentini M.;
2015-01-01

Abstract

Apoptosis-inducing factor (AIF) is a mitochondrial flavoprotein that, beyond its apoptotic function, is required for the normal expression of major respiratory chain complexes. Here we identified an AIF-interacting protein, CHCHD4, which is the central component of a redox-sensitive mitochondrial intermembrane space import machinery. Depletion or hypomorphic mutation of AIF caused a downregulation of CHCHD4 protein by diminishing its mitochondrial import. CHCHD4 depletion sufficed to induce a respiratory defect that mimicked that observed in AIF-deficient cells. CHCHD4 levels could be restored in AIF-deficient cells by enforcing its AIF-independent mitochondrial localization. This modified CHCHD4 protein reestablished respiratory function in AIF-deficient cells and enabled AIF-deficient embryoid bodies to undergo cavitation, a process of programmed cell death required for embryonic morphogenesis. These findings explain how AIF contributes to the biogenesis of respiratory chain complexes, and they establish an unexpected link between the vital function of AIF and the propensity of cells to undergo apoptosis.
2015
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/06 - ANATOMIA COMPARATA E CITOLOGIA
English
Con Impact Factor ISI
Amino Acid Sequence; Animals; Apoptosis Inducing Factor; Cell Line, Tumor; Electron Transport; Electron Transport Chain Complex Proteins; Embryo, Mammalian; Embryonic Development; Humans; Immunoblotting; Mice, Knockout; Mitochondria; Mitochondrial Membrane Transport Proteins; Molecular Sequence Data; Protein Binding; Protein Transport; RNA Interference; Time Factors
Hangen, E., Feraud, O., Lachkar, S., Mou, H., Doti, N., Fimia, G.m., et al. (2015). Interaction between AIF and CHCHD4 Regulates Respiratory Chain Biogenesis. MOLECULAR CELL, 58(6), 1001-1014 [10.1016/j.molcel.2015.04.020].
Hangen, E; Feraud, O; Lachkar, S; Mou, H; Doti, N; Fimia, Gm; Lam, N-; Zhu, C; Godin, I; Muller, K; Chatzi, A; Nuebel, E; Ciccosanti, F; Flamant, S; Benit, P; Perfettini, J-; Sauvat, A; Bennaceur-Griscelli, A; Ser-Le Roux, K; Gonin, P; Tokatlidis, K; Rustin, P; Piacentini, M; Ruvo, M; Blomgren, K; Kroemer, G; Modjtahedi, N
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/233216
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