Drosophila models of human neurodegenerative disease

被引:71
|
作者
Chan, HYE [1 ]
Bonini, NM [1 ]
机构
[1] Univ Penn, Howard Hughes Med Inst, Dept Biol, Philadelphia, PA 19104 USA
来源
CELL DEATH AND DIFFERENTIATION | 2000年 / 7卷 / 11期
基金
英国惠康基金; 美国国家卫生研究院;
关键词
Alzheimer's disease; Parkinson's disease; polyglutamine; molecular chaperones; genetics;
D O I
10.1038/sj.cdd.4400757
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drosophila has provided a powerful genetic system in which to elucidate fundamental cellular pathways in the context of a developing and functioning nervous system. Recently, Drosophila has been applied toward elucidating mechanisms of human neurodegenerative disease, including Alzheimer's, Parkinson's and Huntington's diseases. Drosophila allows study of the normal function of disease proteins, as well as study of effects of familial mutations upon targeted expression of human mutant forms in the fly. These studies have revealed new insight into the normal functions of such disease proteins, as well as provided models in Drosophila that will allow genetic approaches to be applied toward elucidating ways to prevent or delay toxic effects of such disease proteins. These, and studies to come that follow from the recently completed sequence of the Drosophila genome, underscore the contributions that Drosophila as a model genetic system stands to contribute toward the understanding of human neurodegenerative disease.
引用
收藏
页码:1075 / 1080
页数:6
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