Transcriptional dysregulation in Huntington's disease

被引:322
作者
Cha, JHJ [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
关键词
D O I
10.1016/S0166-2236(00)01609-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although the gene responsible for Huntington's disease was discovered in 1993, the pathogenic mechanisms by which mutant huntingtin causes neuronal dysfunction and death remain unclear. However, increasing evidence suggests that mutant huntingtin disrupts the normal transcriptional program of susceptible neurons. Thus, transcriptional dysregulation might be an important pathogenic mechanism in Huntington's disease.
引用
收藏
页码:387 / 392
页数:6
相关论文
共 103 条
  • [81] Recent advances in understanding the pathogenesis of Huntington's disease
    Reddy, PH
    Williams, M
    Tagle, DA
    [J]. TRENDS IN NEUROSCIENCES, 1999, 22 (06) : 248 - 255
  • [82] Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA
    Reddy, PH
    Williams, M
    Charles, V
    Garrett, L
    Pike-Buchanan, L
    Whetsell, WO
    Miller, G
    Tagle, DA
    [J]. NATURE GENETICS, 1998, 20 (02) : 198 - 202
  • [83] The complex pathology of trinucleotide repeats
    Reddy, PS
    Housman, DE
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (03) : 364 - 372
  • [84] Polyglutamine pathogenesis
    Ross, CA
    Wood, JD
    Schilling, G
    Peters, MF
    Nucifora, FC
    Cooper, JK
    Sharp, AH
    Margolis, RL
    Borchelt, DR
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1999, 354 (1386) : 1005 - 1011
  • [85] Intranuclear neuronal inclusions: A common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?
    Ross, CA
    [J]. NEURON, 1997, 19 (06) : 1147 - 1150
  • [86] Caspase-8 is required for cell death induced by expanded polyglutamine repeats
    Sánchez, I
    Xu, CJ
    Juo, P
    Kakizaka, A
    Blenis, J
    Yuan, JY
    [J]. NEURON, 1999, 22 (03) : 623 - 633
  • [87] Huntingtin localization in brains of normal and Huntington's disease patients
    Sapp, E
    Schwarz, C
    Chase, K
    Bhide, PG
    Young, AB
    Penney, J
    Vonsattel, JP
    Aronin, N
    DiFiglia, M
    [J]. ANNALS OF NEUROLOGY, 1997, 42 (04) : 604 - 612
  • [88] Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
    Saudou, F
    Finkbeiner, S
    Devys, D
    Greenberg, ME
    [J]. CELL, 1998, 95 (01) : 55 - 66
  • [89] Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
    Scherzinger, E
    Lurz, R
    Turmaine, M
    Mangiarini, L
    Hollenbach, B
    Hasenbank, R
    Bates, GP
    Davies, SW
    Lehrach, H
    Wanker, EE
    [J]. CELL, 1997, 90 (03) : 549 - 558
  • [90] Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin
    Schilling, G
    Becher, MW
    Sharp, AH
    Jinnah, HA
    Duan, K
    Kotzuk, JA
    Slunt, HH
    Ratovitski, T
    Cooper, JK
    Jenkins, NA
    Copeland, NG
    Price, DL
    Ross, CA
    Borchelt, DR
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (03) : 397 - 407