Barton A J, Crook B W, Karran E H, Brown F, Dewar D, Mann D M, Pearson R C, Graham D I, Hardy J, Hutton M, Duff K, Goate A M, Clark R F, Roberts G W
Department of Molecular Neuropathology Research, SmithKline Beecham Pharmaceuticals, Harlow.
Neurodegeneration. 1996 Sep;5(3):213-8. doi: 10.1006/neur.1996.0029.
The expression of the presenilin 1 (PS-1) gene has been investigated by in situ hybridization 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. The in situ hybridization 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.
通过原位杂交技术,对早发性家族性阿尔茨海默病(FAD)、晚发性阿尔茨海默病(AD)以及正常对照大脑中的早老素1(PS-1)基因表达进行了研究。该基因的突变与14号染色体连锁的FAD有关。我们发现,早老素1信使核糖核酸(mRNA)存在于整个人脑中,其分布与神经胶质细胞和神经元的定位均相符。对照、早发性FAD病例和晚发性AD病例的原位杂交模式相似。然而,与晚发性AD相比,早发性FAD大脑中PS-1的两种mRNA形式之一,即长形式(其5'端包含一个编码四个氨基酸(VRSQ)插入序列)显著减少。我们认为,这种长转录本可能会改变淀粉样前体蛋白的正常加工途径,而淀粉样前体蛋白似乎是AD发病机制的核心蛋白。