Flightless flies: Drosophila models of neuromuscular disease

被引:109
作者
Lloyd, Thomas E. [1 ]
Taylor, J. Paul [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
来源
YEAR IN NEUROLOGY 2 | 2010年 / 1184卷
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; SPINAL MUSCULAR-ATROPHY; TRANSGENIC MOUSE MODEL; MYOTONIC-DYSTROPHY; AXONAL-TRANSPORT; LIFE-SPAN; ANDROGEN RECEPTOR; MOTOR-NEURONS; LATE-ONSET; NEUROTRANSMITTER RELEASE;
D O I
10.1111/j.1749-6632.2010.05432.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The fruit fly, Drosophila melanogaster, has a long and rich history as an important model organism for biologists. In particular, study of the fruit fly has been essential to much of our fundamental understanding of the development and function of the nervous system. In recent years, studies using fruit flies have provided important insights into the pathogenesis of neurodegenerative and neuromuscular diseases. Flymodels of spinalmuscular atrophy, spinobulbar muscular atrophy,myotonic dystrophy, dystrophinopathies and other inherited neuromuscular diseases recapitulate many of the key pathologic features of the human disease. The ability to perform genetic screens holds promise for uncovering the molecular mechanisms of disease, and indeed, for identifying novel therapeutic targets. This review will summarize recent progress in developing fly models of neuromuscular diseases and will emphasize the contribution that Drosophila has made to our understanding of these diseases.
引用
收藏
页码:E1 / E20
页数:20
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