Department of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX USA.
Prion. 2013 Mar-Apr;7(2):164-9. doi: 10.4161/pri.23711. Epub 2013 Jan 29.
Single nucleotide polymorphisms in the ubiquilin-1 gene may confer risk for late-onset Alzheimer disease (AD). We have shown previously that ubiquilin-1 functions as a molecular chaperone for the amyloid precursor protein (APP) and that protein levels of ubiquilin-1 are decreased in the brains of AD patients. We have recently found that ubiquilin-1 regulates APP trafficking and subsequent secretase processing by stimulating non-degradative ubiquitination of a single lysine residue in the cytosolic domain of APP. Thus, ubiquilin-1 plays a central role in regulating APP biosynthesis, trafficking and ultimately toxicity. As ubiquilin-1 and other ubiquilin family members have now been implicated in the pathogenesis of numerous neurodegenerative diseases, these findings provide mechanistic insights into the central role of ubiquilin proteins in maintaining neuronal proteostasis.
泛素结合酶 1 基因单核苷酸多态性可能与晚发性阿尔茨海默病(AD)的发病风险相关。我们之前的研究表明,泛素结合酶 1 作为淀粉样前体蛋白(APP)的分子伴侣发挥作用,并且 AD 患者的大脑中泛素结合酶 1 的蛋白水平降低。我们最近发现,泛素结合酶 1 通过刺激 APP 胞质结构域中单个赖氨酸残基的非降解泛素化,调节 APP 的运输和随后的蛋白酶加工。因此,泛素结合酶 1 在调节 APP 的生物合成、运输和最终毒性方面发挥着核心作用。由于泛素结合酶 1 和其他泛素结合酶家族成员现在已被牵连到许多神经退行性疾病的发病机制中,这些发现为泛素结合酶蛋白在维持神经元蛋白平衡方面的核心作用提供了机制上的见解。