Mitochondrial diseases in man and mouse

被引:2463
作者
Wallace, DC [1 ]
机构
[1] Emory Univ, Ctr Mol Med, Atlanta, GA 30322 USA
关键词
D O I
10.1126/science.283.5407.1482
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Over the past 10 years, mitochondrial defects have been implicated in a wide variety of degenerative diseases, aging, and cancer. Studies on patients with these diseases have revealed much about the complexities of mitochondrial genetics, which involves an interplay between mutations in the mitochondrial and nuclear genomes. However, the pathophysiology of mitochondrial diseases has remained perplexing. The essential role of mitochondrial oxidative phosphorylation in cellular energy production, the generation of reactive oxygen species, and the initiation of apoptosis has suggested a number of novel mechanisms for mitochondrial pathology. The importance and interrelationship of these functions are now being studied in mouse models of mitochondrial disease.
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页码:1482 / 1488
页数:9
相关论文
共 102 条
[1]   OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[2]   The genome sequence of Rickettsia prowazekii and the origin of mitochondria [J].
Andersson, SGE ;
Zomorodipour, A ;
Andersson, JO ;
Sicheritz-Pontén, T ;
Alsmark, UCM ;
Podowski, RM ;
Näslund, AK ;
Eriksson, AS ;
Winkler, HH ;
Kurland, CG .
NATURE, 1998, 396 (6707) :133-140
[3]   MATERNALLY TRANSMITTED DIABETES AND DEAFNESS ASSOCIATED WITH A 10.4 KB MITOCHONDRIAL-DNA DELETION [J].
BALLINGER, SW ;
SHOFFNER, JM ;
HEDAYA, EV ;
TROUNCE, I ;
POLAK, MA ;
KOONTZ, DA ;
WALLACE, DC .
NATURE GENETICS, 1992, 1 (01) :11-15
[4]   MITOCHONDRIAL DIABETES REVISITED [J].
BALLINGER, SW ;
SHOFFNER, JM ;
GEBHART, S ;
KOONTZ, DA ;
WALLACE, DC .
NATURE GENETICS, 1994, 7 (04) :458-459
[5]   MITOCHONDRIAL-DNA OF CHLORAMPHENICOL-RESISTANT MOUSE CELLS CONTAINS A SINGLE NUCLEOTIDE CHANGE IN THE REGION ENCODING THE 3' END OF THE LARGE RIBOSOMAL-RNA [J].
BLANC, H ;
WRIGHT, CT ;
BIBB, MJ ;
WALLACE, DC ;
CLAYTON, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06) :3789-3793
[6]  
BODNAR AG, 1993, AM J HUM GENET, V53, P663
[7]   MUTATION OF A NUCLEAR SUCCINATE-DEHYDROGENASE GENE RESULTS IN MITOCHONDRIAL RESPIRATORY-CHAIN DEFICIENCY [J].
BOURGERON, T ;
RUSTIN, P ;
CHRETIEN, D ;
BIRCHMACHIN, M ;
BOURGEOIS, M ;
VIEGASPEQUIGNOT, E ;
MUNNICH, A ;
ROTIG, A .
NATURE GENETICS, 1995, 11 (02) :144-149
[8]   Mitochondrial ADP/ATP carrier can be reversibly converted into a large channel by Ca2+ [J].
Brustovetsky, N ;
Klingenberg, M .
BIOCHEMISTRY, 1996, 35 (26) :8483-8488
[9]   CYTOPLASMIC INHERITANCE OF CHLORAMPHENICOL RESISTANCE IN MOUSE TISSUE-CULTURE CELLS [J].
BUNN, CL ;
WALLACE, DC ;
EISENSTA.JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (05) :1681-1685
[10]   Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease [J].
Casari, G ;
De Fusco, M ;
Ciarmatori, S ;
Zeviani, M ;
Mora, M ;
Fernandez, P ;
De Michele, G ;
Filla, A ;
Cocozza, S ;
Marconi, R ;
Dürr, A ;
Fontaine, B ;
Ballabio, A .
CELL, 1998, 93 (06) :973-983