Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module

Author:

Jackson Thomas D.12,Crameri Jordan J.12ORCID,Muellner-Wong Linden123ORCID,Frazier Ann E.34,Palmer Catherine S.12,Formosa Luke E.5ORCID,Hock Daniella H.12,Fujihara Kenji M.67ORCID,Stait Tegan38,Sharpe Alice J.5ORCID,Thorburn David R.348ORCID,Ryan Michael T.5ORCID,Stroud David A.123ORCID,Stojanovski Diana12ORCID

Affiliation:

1. Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia

2. Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia

3. Murdoch Children’s Research Institute, Royal Children’s Hospital, Melbourne, VIC 3052, Australia

4. Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia

5. Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3168, Australia

6. Division of Cancer Research, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia

7. Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, VIC 3010, Australia

8. Victorian Clinical Genetic Services, Royal Children’s Hospital, Melbourne, VIC 3052, Australia

Abstract

Significance Mitochondria are double-membraned eukaryotic organelles that house the proteins required for generation of ATP, the energy currency of cells. ATP generation within mitochondria is performed by five multisubunit complexes (complexes I to V), the assembly of which is an intricate process. Mutations in subunits of these complexes, or the suite of proteins that help them assemble, lead to a severe multisystem condition called mitochondrial disease. We show that SFXN4, a protein that causes mitochondrial disease when mutated, assists with the assembly of complex I. This finding explains why mutations in SFXN4 cause mitochondrial disease and is surprising because SFXN4 belongs to a family of amino acid transporter proteins, suggesting that it has undergone a dramatic shift in function through evolution.

Funder

Mito Foundation

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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