Goedert M, Wischik C M, Crowther R A, Walker J E, Klug A
Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom.
Proc Natl Acad Sci U S A. 1988 Jun;85(11):4051-5. doi: 10.1073/pnas.85.11.4051.
Screening of cDNA libraries prepared from the frontal cortex of an Alzheimer disease patient and from fetal human brain has led to isolation of the cDNA for a core protein of the paired helical filament of Alzheimer disease. The partial amino acid sequence of this core protein was used to design synthetic oligonucleotide probes. The cDNA encodes a protein of 352 amino acids that contains a characteristic amino acid repeat in its carboxyl-terminal half. This protein is highly homologous to the sequence of the mouse microtubule-associated protein tau and thus constitutes the human equivalent of mouse tau. RNA blot analysis indicates the presence of two major transcripts, 6 and 2 kilobases lon g, with a wide distribution in normal human brain. Tau protein mRNAs were found in normal amounts in the frontal cortex from patients with Alzheimer disease. The proof that at least part of tau protein forms a component of the paired helical filament core opens the way to understanding the mode of formation of paired helical filaments and thus, ultimately, the pathogenesis of Alzheimer disease.
对取自一名阿尔茨海默病患者额叶皮质以及胎儿人脑的cDNA文库进行筛选,已成功分离出阿尔茨海默病双螺旋丝核心蛋白的cDNA。利用该核心蛋白的部分氨基酸序列设计了合成寡核苷酸探针。该cDNA编码一个由352个氨基酸组成的蛋白质,该蛋白质在其羧基末端的一半含有一个特征性的氨基酸重复序列。此蛋白质与小鼠微管相关蛋白tau的序列高度同源,因此构成了人类的小鼠tau等效物。RNA印迹分析表明存在两种主要转录本,长度分别为6千碱基和2千碱基,在正常人脑中分布广泛。在阿尔茨海默病患者的额叶皮质中发现tau蛋白mRNA含量正常。tau蛋白至少部分构成双螺旋丝核心成分这一证据,为理解双螺旋丝的形成方式进而最终理解阿尔茨海默病的发病机制开辟了道路。