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tau基因突变:剖析额颞叶痴呆伴帕金森综合征17型的发病机制

Tau gene mutations: dissecting the pathogenesis of FTDP-17.

作者信息

Ingram Esther M, Spillantini Maria G

机构信息

Dept of Neurology and Cambridge Centre for Brain Repair, University of Cambridge, UK.

出版信息

Trends Mol Med. 2002 Dec;8(12):555-62. doi: 10.1016/s1471-4914(02)02440-1.

Abstract

Tau is a microtubule-associated protein involved in microtubule assembly and stabilization. Abnormal filamentous tau deposits constitute a major defining characteristic of several neurodegenerative diseases, including Alzheimer's disease. Although the presence of tau pathology correlates with the symptoms of Alzheimer's disease, there was no genetic evidence linking tau to neurodegeneration until recently. However, since 1998, the identification of more than 25 mutations in the tau gene, associated with frontotemporal dementia and parkinsonism linked to chromosome 17, has demonstrated that tau dysfunction can lead to neurodegeneration and the development of clinical symptoms.

摘要

tau蛋白是一种与微管相关的蛋白质,参与微管的组装和稳定。异常的丝状tau蛋白沉积物是包括阿尔茨海默病在内的几种神经退行性疾病的主要决定性特征。尽管tau蛋白病理学的存在与阿尔茨海默病的症状相关,但直到最近才有将tau蛋白与神经退行性变联系起来的遗传学证据。然而,自1998年以来,在tau基因中鉴定出25种以上与17号染色体相关的额颞叶痴呆和帕金森综合征相关的突变,这表明tau蛋白功能障碍可导致神经退行性变和临床症状的发展。

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