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Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module.
Jackson, Thomas D; Crameri, Jordan J; Muellner-Wong, Linden; Frazier, Ann E; Palmer, Catherine S; Formosa, Luke E; Hock, Daniella H; Fujihara, Kenji M; Stait, Tegan; Sharpe, Alice J; Thorburn, David R; Ryan, Michael T; Stroud, David A; Stojanovski, Diana.
Afiliación
  • Jackson TD; Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Crameri JJ; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Muellner-Wong L; Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Frazier AE; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Palmer CS; Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Formosa LE; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Hock DH; Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
  • Fujihara KM; Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
  • Stait T; Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia.
  • Sharpe AJ; Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Thorburn DR; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Ryan MT; Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3168, Australia.
  • Stroud DA; Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Stojanovski D; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
Proc Natl Acad Sci U S A ; 119(13): e2115566119, 2022 03 29.
Article en En | MEDLINE | ID: mdl-35333655
ABSTRACT
SignificanceMitochondria 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Complejo I de Transporte de Electrón Límite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Complejo I de Transporte de Electrón Límite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article País de afiliación: Australia