早发性家族性阿尔茨海默病中脑早老素1 mRNA表达的改变

Amanda J.L. Barton , Barry W. Crook , Eric H. Karran , Frank Brown , Deborah Dewar , David M.A. Mann , R.Carl A. Pearson , David I. Graham , John Hardy , Mike Hutton , Karen Duff , Alison M. Goate , Robert F. Clark , Gareth W. Roberts
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引用次数: 12

摘要

采用原位杂交技术研究了早老素1 (PS-1)基因在早发性家族性阿尔茨海默病(FAD)、晚发性阿尔茨海默病(AD)和正常对照脑中的表达。该基因的突变导致了14号染色体相关的FAD。我们发现早老素1 mRNA存在于整个人脑中,其分布与胶质和神经元定位一致。在对照组、早发性FAD病例和晚发性AD病例中,它们的位置杂交模式相似。然而,PS-1 mRNA的两种形式之一,长形式(在其5 '端包含一个编码四个氨基酸(VRSQ)插入的序列)在早发性FAD大脑中与晚发性AD相比显着减少。我们认为这种长转录可能改变了淀粉样前体蛋白加工的正常途径,而淀粉样前体蛋白似乎是AD发病机制的核心。
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Alteration in Brain Presenilin 1 mRNA Expression in Early Onset Familial Alzheimer's Disease

The expression of the presenilin 1 (PS–1) gene has been investigated byin situhybridization in early onset familial Alzheimer's disease (FAD), late onset Alzheimer's disease (AD) and normal control brain. Mutations in this gene are responsible for chromosome 14–linked FAD. We have found that presenilin 1 mRNA is present throughout the human brain with a distribution consistent with both a glial and neuronal localization. Thein situhybridization pattern was similar for the controls, the early onset FAD cases and the late onset AD cases. However, one of the two forms of the mRNA for PS–1, the long form (which contains a sequence encoding a four amino acid (VRSQ) insert at its 5′end) was significantly reduced in early onset FAD brain compared with late onset AD. We suggest that this long transcript may alter the normal pathway for processing of amyloid precursor protein, the protein which appears to be central in the pathogenesis of AD.

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