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[与齿状核红核苍白球路易体萎缩症相互作用蛋白的cDNA克隆及特性分析]

[Cloning and characterization of cDNA for DRPLA interacting protein].

作者信息

Okamumoho Y, Yamada M

出版信息

Nihon Rinsho. 1999 Apr;57(4):856-61.

Abstract

Dentatorubral-pallidoluysian atrophy (DRPLA) is associated with CAG repeat expansion. While the DRPLA gene is ubiquitously expressed, neuron death occurs in specific area of the brain, predicting that the DRPLA protein interacts with other proteins, which may play a role in the pathogenesis. We isolated a DRPLA binding protein with a yeast two-hybrid system, and identified it to be a human homologue of insulin receptor substrate protein of 53 kDa (IRSp53). The binding of the DRPLA protein with IRSp53 was ascertained by co-immunoprecipitation, and colocalization. A proline-rich region near polyglutamine of the DRPLA protein and the SH3 domain of IRSp53 were involved in the binding. Extended polyglutamine significantly reduced the binding ability in yeast cells.

摘要

齿状核红核苍白球路易体萎缩症(DRPLA)与CAG重复序列扩增有关。虽然DRPLA基因在全身广泛表达,但神经元死亡发生在大脑的特定区域,这预示着DRPLA蛋白与其他蛋白相互作用,而这些蛋白可能在发病机制中起作用。我们用酵母双杂交系统分离出一种DRPLA结合蛋白,并鉴定其为53 kDa胰岛素受体底物蛋白(IRSp53)的人类同源物。通过免疫共沉淀和共定位确定了DRPLA蛋白与IRSp53的结合。DRPLA蛋白多聚谷氨酰胺附近的富含脯氨酸区域和IRSp53的SH3结构域参与了这种结合。延长的多聚谷氨酰胺显著降低了酵母细胞中的结合能力。

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