Human mitochondrial complex I assembly is mediated by NDUFAF1

Complex I (NADH:ubiquinone oxidoreductase) is the largest multiprotein enzyme of the oxidative phosphorylation system. Its assembly in human cells is poorly understood and no proteins assisting this process have yet been described. A good candidate is NDUFAF1, the human homologue of Neurospora crassa complex I chaperone CIA30. Here, we demonstrate that NDUFAF1 is a mitochondrial protein that is involved in the complex I assembly process. Modulating the intramitochondrial amount of NDUFAF1 by knocking down its expression using RNA interference leads to a reduced amount and activity of complex I. NDUFAF1 is associated to two complexes of 600 and 700 kDa in size of which the relative distribution is altered in two complex I deficient patients. Analysis of NDUFAF1 expression in a conditional complex I assembly system shows that the 700 kDa complex may represent a key step in the complex I assembly process. Based on these data, we propose that NDUFAF1 is an important protein for the assembly/stability of complex I.

[1]  P. Bénit,et al.  AIF deficiency compromises oxidative phosphorylation , 2004, The EMBO journal.

[2]  Rutger O. Vogel,et al.  Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. , 2004, Human molecular genetics.

[3]  N. Yadava,et al.  Development and Characterization of a Conditional Mitochondrial Complex I Assembly System* , 2004, Journal of Biological Chemistry.

[4]  M. Finel,et al.  Assembly of Respiratory Complexes I, III, and IV into NADH Oxidase Supercomplex Stabilizes Complex I in Paracoccus denitrificans* , 2004, Journal of Biological Chemistry.

[5]  A. Vinogradov Respiratory Complex I: Structure, Redox Components, and Possible Mechanisms of Energy Transduction , 2001, Biochemistry (Moscow).

[6]  E. Shoubridge,et al.  Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency* , 2003, Journal of Biological Chemistry.

[7]  J. Hirst,et al.  The nuclear encoded subunits of complex I from bovine heart mitochondria. , 2003, Biochimica et biophysica acta.

[8]  J. Hirst,et al.  Analysis of the Subunit Composition of Complex I from Bovine Heart Mitochondria*S , 2003, Molecular & Cellular Proteomics.

[9]  C. Remacle,et al.  Impact of mutations affecting ND mitochondria-encoded subunits on the activity and assembly of complex I in Chlamydomonas. Implication for the structural organization of the enzyme. , 2002, Journal of molecular biology.

[10]  N. Henderson,et al.  Blue Native electrophoresis to study mitochondrial and other protein complexes. , 2002, Methods.

[11]  P. Rustin,et al.  Cytochrome oxidase in health and disease. , 2002, Gene.

[12]  J. Smeitink,et al.  CIA30 complex I assembly factor: a candidate for human complex I deficiency? , 2002, Human Genetics.

[13]  U. Schulte Biogenesis of Respiratory Complex I , 2001, Journal of bioenergetics and biomembranes.

[14]  S. Dimauro,et al.  The genetics and pathology of oxidative phosphorylation , 2001, Nature Reviews Genetics.

[15]  V. Tiranti,et al.  A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients , 2001, Annals of neurology.

[16]  M. Duarte,et al.  Respiratory chain complex I is essential for sexual development in neurospora and binding of iron sulfur clusters are required for enzyme assembly. , 2000, Genetics.

[17]  N Grigorieff,et al.  Structure of the respiratory NADH:ubiquinone oxidoreductase (complex I) , 1999, Current opinion in structural biology.

[18]  R. Küffner,et al.  Involvement of two novel chaperones in the assembly of mitochondrial NADH:Ubiquinone oxidoreductase (complex I). , 1998, Journal of molecular biology.

[19]  A Videira,et al.  Complex I from the fungus Neurospora crassa. , 1998, Biochimica et biophysica acta.