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Parkinsonism Due to Mutations in PINK1 Parkin and DJ-1 and Oxidative Stress and Mitochondrial Pathways

机译:由于PINK1Parkin和DJ-1突变以及氧化应激和线粒体途径而引起的帕金森病。

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摘要

Three genes have been identified that cause, in humans, autosomally inherited parkinsonism. These are PARK2, encoding the E3 ubiquitin ligase parkin; PINK1, a mitochondrial kinase; and PARK7, which codes for the protein DJ-1. In several experimental systems, it has been shown that all three proteins impact mitochondrial function and/or oxidative stress responses. These are probably related because mitochondria produce oxidative stress in neurons. Moreover, it is clear that there are relationships between these genes, with a single pathway linking PINK1 and parkin and a parallel relationship with DJ-1. Work in progress in the field is aimed at understanding these relationships in more depth.
机译:已经鉴定出三种基因,它们在人类中引起自体遗传的帕金森病。它们是PARK2,编码E3泛素连接酶parkin; PINK1,线粒体激酶;和PARK7,其编码蛋白质DJ-1。在几个实验系统中,已显示所有三种蛋白质均影响线粒体功能和/或氧化应激反应。这些可能是相关的,因为线粒体在神经元中产生氧化应激。而且,很明显,这些基因之间存在联系,通过单个途径连接PINK1和parkin,与DJ-1平行。该领域的工作旨在更深入地了解这些关系。

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