| Literature DB >> 26004228 |
Emilie Hangen1, Olivier Féraud2, Sylvie Lachkar1, Haiwei Mou1, Nunzianna Doti3, Gian Maria Fimia4, Ngoc-Vy Lam1, Changlian Zhu5, Isabelle Godin6, Kevin Muller1, Afroditi Chatzi7, Esther Nuebel7, Fabiola Ciccosanti8, Stéphane Flamant9, Paule Bénit10, Jean-Luc Perfettini11, Allan Sauvat12, Annelise Bennaceur-Griscelli13, Karine Ser-Le Roux14, Patrick Gonin14, Kostas Tokatlidis7, Pierre Rustin10, Mauro Piacentini15, Menotti Ruvo3, Klas Blomgren16, Guido Kroemer17, Nazanine Modjtahedi18.
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26004228 DOI: 10.1016/j.molcel.2015.04.020
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970