Human mitochondrial complex I assembly is mediated by NDUFAF1

被引:114
作者
Vogel, RO
Janssen, RJRJ
Ugalde, C
Grovenstein, M
Huijbens, RJ
Visch, HJ
van den Heuvel, LP
Willems, PH
Zeviani, M
Smeitink, JAM
Nijtmans, LGJ
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Paediat, Nijmegen Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, Netherlands
[2] Hosp Univ 12 Octubre, Ctr Invest, Madrid, Spain
[3] Radboud Univ Nijmegen, Med Ctr, Dept Biochem, NL-6500 HB Nijmegen, Netherlands
[4] Natl Inst Neurol C Besta, Unit Mol Neurogenet, Milan, Italy
关键词
assembly; NDUFAF1; complex I; mitochondria; oxidative phosphorylation;
D O I
10.1111/j.1742-4658.2005.04928.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:5317 / 5326
页数:10
相关论文
共 20 条
[1]   Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency [J].
Antonicka, H ;
Ogilvie, I ;
Taivassalo, T ;
Anitori, RP ;
Haller, RG ;
Vissing, J ;
Kennaway, NG ;
Shoubridge, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) :43081-43088
[2]   Cytochrome oxidase in health and disease [J].
Barrientos, A ;
Barros, MH ;
Valnot, I ;
Rötig, A ;
Rustin, P ;
Tzagoloff, A .
GENE, 2002, 286 (01) :53-63
[3]   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 [J].
Cardol, P ;
Matagne, RF ;
Remacle, C .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 319 (05) :1211-1221
[4]   Analysis of the subunit composition of complex I from bovine heart mitochondria [J].
Carroll, J ;
Fearnley, IM ;
Shannon, RJ ;
Hirst, J ;
Walker, JE .
MOLECULAR & CELLULAR PROTEOMICS, 2003, 2 (02) :117-126
[5]  
Corona P, 2001, ANN NEUROL, V49, P106, DOI 10.1002/1531-8249(200101)49:1<106::AID-ANA16>3.0.CO
[6]  
2-T
[7]  
Duarte M, 2000, GENETICS, V156, P607
[8]   Structure of the respiratory NADH:ubiquinone oxidoreductase (complex I) [J].
Grigorieff, N .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1999, 9 (04) :476-483
[9]   The nuclear encoded subunits of complex I from bovine heart mitochondria [J].
Hirst, J ;
Carroll, J ;
Fearnley, IM ;
Shannon, RJ ;
Walker, JE .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2003, 1604 (03) :135-150
[10]   CIA30 complex I assembly factor: a candidate for human complex I deficiency? [J].
Janssen, R ;
Smeitink, J ;
Smeets, R ;
van den Heuvel, L .
HUMAN GENETICS, 2002, 110 (03) :264-270