Cytoplasmic dynein could be key to understanding neurodegeneration

被引:26
作者
Banks, Gareth T. [1 ]
Fisher, Elizabeth M. C. [1 ]
机构
[1] Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1186/gb-2008-9-3-214
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A new mouse mutation, Sprawling, highlights an essential role for the dynein heavy chain in sensory neuron function, but it lacks the ability of other known heavy-chain mutations to ameliorate neurodegeneration due to defective superoxide dismutase.
引用
收藏
页数:4
相关论文
共 21 条
[1]   Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic dynein heavy chain 1 gene [J].
Chen, Xiang-Jun ;
Levedakou, Eleni N. ;
Millen, Kathleen J. ;
Wollmann, Robert L. ;
Soliven, Betty ;
Popko, Brian .
JOURNAL OF NEUROSCIENCE, 2007, 27 (52) :14515-14524
[2]   Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content [J].
De Vos, Kurt J. ;
Chapman, Anna L. ;
Tennant, Maria E. ;
Manser, Catherine ;
Tudor, Elizabeth L. ;
Lau, Kwok-Fai ;
Brownlees, Janet ;
Ackerley, Steven ;
Shaw, Pamela J. ;
McLoughlin, Declan M. ;
Shaw, Christopher E. ;
Leigh, P. Nigel ;
Miller, Christopher C. J. ;
Grierson, Andrew J. .
HUMAN MOLECULAR GENETICS, 2007, 16 (22) :2720-2728
[3]   Dynein is required for receptor sorting and the morphogenesis of early endosomes [J].
Driskell, Owen J. ;
Mironov, Aleksandr ;
Allan, Victoria J. ;
Woodman, Philip G. .
NATURE CELL BIOLOGY, 2007, 9 (01) :113-U152
[4]   Mutations in dynein link motor neuron degeneration to defects in retrograde transport [J].
Hafezparast, M ;
Klocke, R ;
Ruhrberg, C ;
Marquardt, A ;
Ahmad-Annuar, A ;
Bowen, S ;
Lalli, G ;
Witherden, AS ;
Hummerich, H ;
Nicholson, S ;
Morgan, PJ ;
Oozageer, R ;
Priestley, JV ;
Averill, S ;
King, VR ;
Ball, S ;
Peters, J ;
Toda, T ;
Yamamoto, A ;
Hiraoka, Y ;
Augustin, M ;
Korthaus, D ;
Wattler, S ;
Wabnitz, P ;
Dickneite, C ;
Lampel, S ;
Boehme, F ;
Peraus, G ;
Popp, A ;
Rudelius, M ;
Schlegel, J ;
Fuchs, H ;
de Angelis, MH ;
Schiavo, G ;
Shima, DT ;
Russ, AP ;
Stumm, G ;
Martin, JE ;
Fisher, EMC .
SCIENCE, 2003, 300 (5620) :808-812
[5]   Golgi vesiculation and lysosome dispersion in cells lacking cytoplasmic dynein [J].
Harada, A ;
Takei, Y ;
Kanai, Y ;
Tanaka, Y ;
Nonaka, S ;
Hirokawa, N .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :51-59
[6]   PIN: An associated protein inhibitor of neuronal nitric oxide synthase [J].
Jaffrey, SR ;
Snyder, SH .
SCIENCE, 1996, 274 (5288) :774-777
[7]   Cytoplasmic dynein and dynactin in cell division and intracellular transport [J].
Karki, S ;
Holzbaur, ELF .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (01) :45-53
[8]   A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice [J].
Kieran, D ;
Hafezparast, M ;
Bohnert, S ;
Dick, JRT ;
Martin, J ;
Schiavo, G ;
Fisher, EMC ;
Greensmith, L .
JOURNAL OF CELL BIOLOGY, 2005, 169 (04) :561-567
[9]  
King SM, 2000, J CELL SCI, V113, P2521
[10]   Dazl can bind to dynein motor complex and may play a role in transport of specific mRNAs [J].
Lee, Kyung Ho ;
Lee, Seongju ;
Kim, Byunghyuk ;
Chang, Sunghoe ;
Kim, Soo Woong ;
Paick, Jae-Seung ;
Rhee, Kunsoo .
EMBO JOURNAL, 2006, 25 (18) :4263-4270