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Different effects of Alzheimer-associated mutations of presenilin 1 on its processing.

机译:早老蛋白1的早老性痴呆相关突变对其加工的不同影响。

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摘要

Presenilin 1 (PS 1) shows missense mutations in most early-onset familial Alzheimer's disease (FAD). Transfection of cDNA for wild type PS 1 into rat pheochromocytoma PC12 cells generated a 47 kDa full-size PS 1 protein, which was processed into a 28 kDa N-terminal fragment and a 19 kDa C-terminal fragment. We prepared selected Alzheimer-associated mutations (Gly384Ala, Leu392Val, and Cys410Tyr) of PS 1, which localized after a possible cleavage site. By transient expression in PC12 cells and rat glioma cell line, C6, we examined their influence on the processing of PS 1. Cys410Tyr inhibited proteolytic processing of PS 1, while Gly384Ala and Leu392Val did not. Thus, the Alzheimer related mutations can be divided into two groups in terms of their effect on the proteolytic cleavage of PS 1.
机译:早老素1(PS 1)在大多数早期发作的家族性阿尔茨海默氏病(FAD)中显示出错义突变。将野生型PS 1的cDNA转染到大鼠嗜铬细胞瘤PC12细胞中产生了47 kDa的全尺寸PS 1蛋白,该蛋白被加工成28 kDa的N端片段和19 kDa的C端片段。我们准备了PS 1的选定的与阿尔茨海默氏症相关的突变(Gly384Ala,Leu392Val和Cys410Tyr),该突变位于可能的切割位点之后。通过在PC12细胞和大鼠神经胶质瘤细胞系C6中的瞬时表达,我们检查了它们对PS 1加工的影响。Cys410Tyr抑制了PS 1的蛋白水解加工,而Gly384Ala和Leu392Val没有。因此,就其对PS 1的蛋白水解裂解的影响而言,与阿尔茨海默氏症相关的突变可分为两组。

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