Recent advances in the molecular basis of inherited photoreceptor degeneration

被引:33
作者
Clarke, G
Héon, E
McInnes, RR
机构
[1] Hosp Sick Children, Res Inst, Program Dev Biol, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Res Inst, Genet Program, Toronto, ON M5G 1X8, Canada
[3] Univ Hlth Network, Vis Res Program, Toronto, ON M5T 2S8, Canada
[4] Univ Toronto, Dept Pediat, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[6] Univ Toronto, Dept Ophthalmol, Toronto, ON M5S 1A8, Canada
关键词
D O I
10.1034/j.1399-0004.2000.570501.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To date, 118 loci have been associated with photoreceptor degenerative disease. In this review, we will discuss recent advances in the identification of genes that cause progressive photoreceptor cell death when mutated. We will focus on 12 genes isolated within the last two years that have been shown to be photoreceptor-specific, or that have provided insight into photoreceptor biology and the mechanisms of photoreceptor cell death. To aid in understanding the biologic basis for these diseases, we also briefly review photoreceptor biology. Finally, we report on recent advances towards the treatment of these disorders.
引用
收藏
页码:313 / 329
页数:17
相关论文
共 150 条
  • [11] Bennett J, 1997, INVEST OPHTH VIS SCI, V38, P2857
  • [12] Adenovirus-mediated delivery of rhodopsin-promoted bcl-2 results in a delay in photoreceptor cell death in the rd/rd mouse
    Bennett, J
    Zeng, Y
    Bajwa, R
    Klatt, L
    Li, Y
    Maguire, AM
    [J]. GENE THERAPY, 1998, 5 (09) : 1156 - 1164
  • [13] A RANDOMIZED TRIAL OF VITAMIN-A AND VITAMIN-E SUPPLEMENTATION FOR RETINITIS-PIGMENTOSA
    BERSON, EL
    ROSNER, B
    SANDBERG, MA
    HAYES, KC
    NICHOLSON, BW
    WEIGELDIFRANCO, C
    WILLETT, W
    [J]. ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (06) : 761 - 772
  • [14] BERSON EL, 1994, PRINCIPLES PRACTICE, P1214
  • [15] BESSANT DAR, 1999, NAT GENET, V21, P255
  • [16] CLOSE GENETIC-LINKAGE BETWEEN X-LINKED RETINITIS PIGMENTOSA AND A RESTRICTION FRAGMENT LENGTH POLYMORPHISM IDENTIFIED BY RECOMBINANT DNA PROBE L1.28
    BHATTACHARYA, SS
    WRIGHT, AF
    CLAYTON, JF
    PRICE, WH
    PHILLIPS, CI
    MCKEOWN, CME
    JAY, M
    BIRD, AC
    PEARSON, PL
    SOUTHERN, EM
    EVANS, HJ
    [J]. NATURE, 1984, 309 (5965) : 253 - 255
  • [17] Bird AC, 1998, OX MG MED G, P325
  • [18] BROWNE SJ, 1999, HUM MOL GENET, V8, P2121
  • [19] Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa
    Buraczynska, M
    Wu, WP
    Fujita, R
    Buraczynska, K
    Phelps, E
    Andréasson, S
    Bennett, J
    Birch, DG
    Fishman, GA
    Hoffman, DR
    Inana, G
    Jacobson, SG
    Musarella, MA
    Sieving, PA
    Swaroop, A
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (06) : 1287 - 1292
  • [20] An evaluation of the role of mitochondria in neurodegenerative diseases: mitochondrial mutations and oxidative pathology, protective nuclear responses, and cell death in neurodegeneration
    Cassarino, DS
    Bennett, JP
    [J]. BRAIN RESEARCH REVIEWS, 1999, 29 (01) : 1 - 25