Diseases of unstable repeat expansion: Mechanisms and common principles

被引:597
作者
Gatchel, JR
Zoghbi, HY [1 ]
机构
[1] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Howard Hughes Med Inst, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Neurosci, Med Sci Training Program, Houston, TX 77030 USA
关键词
D O I
10.1038/nrg1691
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The list of developmental and degenerative diseases that are caused by expansion of unstable repeats continues to grow, and is now approaching 20 disorders. The pathogenic mechanisms that underlie these disorders involve either loss of protein function or gain of function at the protein or RNA level. Common themes have emerged within and between these different classes of disease; for example, among disorders that are caused by gain-of-function mechanisms, altered protein conformations are central to pathogenesis, leading to changes in protein activity or abundance. In all these diseases, the context of the expanded repeat and the abundance, subcellular localization and interactions of the proteins and RNAs that are affected have key roles in disease-specific phenotypes.
引用
收藏
页码:743 / 755
页数:13
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共 155 条
  • [11] Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
    Campuzano, V
    Montermini, L
    Molto, MD
    Pianese, L
    Cossee, M
    Cavalcanti, F
    Monros, E
    Rodius, F
    Duclos, F
    Monticelli, A
    Zara, F
    Canizares, J
    Koutnikova, H
    Bidichandani, SI
    Gellera, C
    Brice, A
    Trouillas, P
    DeMichele, G
    Filla, A
    DeFrutos, R
    Palau, F
    Patel, PI
    DiDonato, S
    Mandel, JL
    Cocozza, S
    Koenig, M
    Pandolfo, M
    [J]. SCIENCE, 1996, 271 (5254) : 1423 - 1427
  • [12] Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes
    Campuzano, V
    Montermini, L
    Lutz, Y
    Cova, L
    Hindelang, C
    Jiralerspong, S
    Trottier, Y
    Kish, SJ
    Faucheux, B
    Trouillas, P
    Authier, FJ
    Durr, A
    Mandel, JL
    Vescovi, A
    Pandolfo, M
    Koenig, M
    [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (11) : 1771 - 1780
  • [13] Fragile X-related protein and VIG associate with the RNA interference machinery
    Caudy, AA
    Myers, M
    Hannon, GJ
    Hammond, SM
    [J]. GENES & DEVELOPMENT, 2002, 16 (19) : 2491 - 2496
  • [14] Mechanisms of chaperone suppression of polyglutamine disease:: selectivity, synergy and medullation of protein solubility in Drosophila
    Chan, HYE
    Warrick, JM
    Gray-Board, GL
    Paulson, HL
    Bonini, NM
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (19) : 2811 - 2820
  • [15] Disabled early recruitment of antioxidant defenses in Friedreich's ataxia
    Chantrel-Groussard, K
    Geromel, V
    Puccio, H
    Koenig, M
    Munnich, A
    Rötig, A
    Rustin, P
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (19) : 2061 - 2067
  • [16] Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
    Charlet-B, N
    Savkur, RS
    Singh, G
    Philips, AV
    Grice, EA
    Cooper, TA
    [J]. MOLECULAR CELL, 2002, 10 (01) : 45 - 53
  • [17] Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1
    Chen, HK
    Fernandez-Funez, P
    Acevedo, SF
    Lam, YC
    Kaytor, MD
    Fernandez, MH
    Aitken, A
    Skoulakis, EMC
    Orr, HT
    Botas, J
    Zoghbi, HY
    [J]. CELL, 2003, 113 (04) : 457 - 468
  • [18] The ubiquitin proteasome system in neurodegenerative diseases: Sometimes the chicken, sometimes the egg
    Ciechanover, A
    Brundin, P
    [J]. NEURON, 2003, 40 (02) : 427 - 446
  • [19] The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes
    Corbin, F
    Bouillon, M
    Fortin, A
    Morin, S
    Rousseau, F
    Khandjian, EW
    [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (09) : 1465 - 1472
  • [20] Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation
    Cossée, M
    Puccio, H
    Gansmuller, A
    Koutnikova, H
    Dierich, A
    LeMeur, M
    Fischbeck, K
    Dollé, P
    Koenig, M
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (08) : 1219 - 1226