The genetics and pathology of oxidative phosphorylation

被引:527
作者
Smeitink, J
van den Heuvel, L
DiMauro, S
机构
[1] Univ Nijmegen, Med Ctr, Dept Paediat, Nijmegen Ctr Mitochondrial Disorders, NL-6500 HB Nijmegen, Netherlands
[2] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
关键词
D O I
10.1038/35072063
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mitochondrial oxidative phosphorylation (OXPHOS) system is the final biochemical pathway in the production of ATP. The OXPHOS system consists of five multiprotein complexes, the individual subunits of which are encoded either by the mitochondrial or by the nuclear genome. Defects in the OXPHOS system result in devastating, mainly multisystem, diseases, and recent years have seen the description of the underlying genetic mutations in mitochondrial and nuclear genes. Advances in this arena have profited from progress in various genome projects, as well as improvements in our ability to create relevant animal models.
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页码:342 / 352
页数:11
相关论文
共 131 条
[1]   Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome [J].
Adams, PL ;
Lightowlers, RN ;
Turnbull, DM .
ANNALS OF NEUROLOGY, 1997, 41 (02) :268-270
[2]   Application of the obligate aerobic yeast Yarrowia lipolytica as a eucaryotic model to analyse Leigh syndrome mutations in the complex I core subunits PSST and TYKY [J].
Ahlers, PM ;
Garofano, A ;
Kerscher, SJ ;
Brandt, U .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2000, 1459 (2-3) :258-265
[4]   FRACTIONATION OF MITOCHONDRIAL RNA FROM HELA-CELLS BY HIGH-RESOLUTION ELECTROPHORESIS UNDER STRONGLY DENATURING CONDITIONS [J].
AMALRIC, F ;
MERKEL, C ;
GELFAND, R ;
ATTARDI, G .
JOURNAL OF MOLECULAR BIOLOGY, 1978, 118 (01) :1-25
[5]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[6]   Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA [J].
Andreu, AL ;
Hanna, MG ;
Reichmann, H ;
Bruno, C ;
Penn, AS ;
Tanji, K ;
Pallotti, F ;
Iwata, S ;
Bonilla, E ;
Lach, B ;
Morgan-Hughes, J ;
DiMauro, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (14) :1037-1044
[7]   Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA [J].
Andrews, RM ;
Kubacka, I ;
Chinnery, PF ;
Lightowlers, RN ;
Turnbull, DM ;
Howell, N .
NATURE GENETICS, 1999, 23 (02) :147-147
[8]  
APRILLE J R, 1991, Current Opinion in Pediatrics, V3, P1045, DOI 10.1097/00008480-199112000-00019
[9]  
ATTARDI G, 1981, TIBS LETT, P86
[10]  
BARRELL BG, 1979, NATURE, V282, P189, DOI 10.1038/282189a0