Drosophila Models of Neurodegenerative Disease

Tzu-Kang Sang, George R. Jackson
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引用次数: 111

Abstract

Over the last two decades, a number of mutations have been identified that give rise to neurodegenerative disorders, including familial forms of Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. Although in most cases sporadic cases vastly outnumber familial forms of such diseases, study of such inherited forms has the potential to provide powerful clues regarding the pathophysiological basis of neurodegeneration. One powerful approach to analyzing disease mechanisms is the development of transgenic animal models, most notably in the mouse. However, development and analysis of such models can be costly and time consuming. Development of improved transgenic technologies have contributed to the development of Drosophila models of a number of neurodegenerative disorders that have shown striking similarities to the human diseases. Moreover, genetic screens using such models have begun to unravel aspects of the pathophysiological basis of neurodegenerative disorders. Here, we provide a general overview of fly models pertinent to trinucleotide repeat expansion disorders, Alzheimer's, and Parkinson's diseases, and highlight key genetic modifiers that have been identified to date using such models.

神经退行性疾病的果蝇模型
在过去的二十年里,已经确定了一些引起神经退行性疾病的突变,包括家族性阿尔茨海默病、帕金森病和肌萎缩性侧索硬化症。尽管在大多数情况下,散发性病例的数量远远超过此类疾病的家族性形式,但对此类遗传形式的研究有可能为神经变性的病理生理基础提供强有力的线索。一种分析疾病机制的有力方法是开发转基因动物模型,尤其是在小鼠身上。然而,这种模型的开发和分析可能是昂贵和耗时的。改良转基因技术的发展促进了许多神经退行性疾病的果蝇模型的发展,这些模型显示出与人类疾病惊人的相似性。此外,使用这种模型的遗传筛选已经开始揭示神经退行性疾病病理生理基础的各个方面。在这里,我们提供了与三核苷酸重复扩增障碍、阿尔茨海默病和帕金森病相关的苍蝇模型的总体概述,并强调了迄今为止使用这些模型已确定的关键遗传修饰因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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