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表达早老素1突变的细胞系中β淀粉样蛋白42(43)增加。

Increased Abeta42(43) from cell lines expressing presenilin 1 mutations.

作者信息

Mehta N D, Refolo L M, Eckman C, Sanders S, Yager D, Perez-Tur J, Younkin S, Duff K, Hardy J, Hutton M

机构信息

Mayo Clinic Jacksonville, FL 32224, USA.

出版信息

Ann Neurol. 1998 Feb;43(2):256-8. doi: 10.1002/ana.410430217.

Abstract

Mutations in the presenilin 1 (PS1) gene on chromosome 14 are a major cause of autosomal dominant, early-onset Alzheimer's disease. Here, we show that transfecting cells with several mutant, but not wild-type, PS1 cDNAs alters the processing of the amyloid precursor protein (APP) such that more Abeta42(43) is produced, confirming and extending several recent reports. The most effective mutation in this regard was the exon 9 splice-out mutation (delta9). The correlation between the size of the effect on APP processing and the age of onset of disease assessed in families with the mutations was not informative, and the possible reasons for this are discussed.

摘要

位于14号染色体上的早老素1(PS1)基因突变是常染色体显性、早发性阿尔茨海默病的主要病因。在此,我们发现用几种突变型而非野生型的PS1互补DNA转染细胞,会改变淀粉样前体蛋白(APP)的加工过程,从而产生更多的Aβ42(43),这证实并扩展了最近的几项报道。在这方面最有效的突变是外显子9缺失突变(delta9)。在有这些突变的家族中,对APP加工影响的大小与疾病发病年龄之间的相关性并无指导意义,文中对此可能的原因进行了讨论。

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