Jacobsen J S, Blume A J, Vitek M P
Central Nervous System Biological Research Department, American Cyanamid Company, Pearl River, NY 10965.
Neurobiol Aging. 1991 Sep-Oct;12(5):585-92. doi: 10.1016/0197-4580(91)90090-7.
We have used an S1 nuclease protection strategy to measure alternatively spliced amyloid precursor protein (APP) mRNAs associated with Alzheimer's disease (AD) to determine whether the expression of either one or more of the transcripts correlate with observed amyloid plaque pathology. Comparison of AD with normal cortex reveals that increasing plaque density parallels an increase in the fraction of APP-695 and a corresponding decrease in APP-770 and 751 mRNA fractions. A specific increase of APP-695, the protease inhibitor-lacking APP RNA form, in those brain regions most involved with amyloid plaque formation, suggests that an imbalance in the protease inhibitor is potentially significant in the disease. These data are consistent with cellular/tissue region-specific regulation of alternative splicing accounting for AD-related changes in the expression of APP mRNA forms.
我们采用了S1核酸酶保护策略来检测与阿尔茨海默病(AD)相关的可变剪接淀粉样前体蛋白(APP)mRNA,以确定一种或多种转录本的表达是否与观察到的淀粉样斑块病理相关。将AD与正常皮质进行比较发现,斑块密度的增加与APP-695比例的增加以及APP-770和751 mRNA比例的相应降低平行。在那些与淀粉样斑块形成最相关的脑区,缺乏蛋白酶抑制剂的APP RNA形式APP-695特异性增加,这表明蛋白酶抑制剂的失衡在该疾病中可能具有重要意义。这些数据与可变剪接的细胞/组织区域特异性调节一致,这种调节解释了APP mRNA形式表达中与AD相关的变化。