Department of Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
Neurodegener Dis. 2010;7(1-3):76-9. doi: 10.1159/000285510. Epub 2010 Feb 18.
Sporadic forms of Alzheimer's and Parkinson's diseases are the most frequent forms of their kind. Together with Huntington's disease, they belong to the so called 'conformational diseases' as they share a common feature in the accumulation of insoluble protein deposits. In this review, we focus on the significance of the ubiquitin-proteasome system in conformational diseases and the possible consequences due to the accumulation of aberrant proteins. In all forms of Alzheimer's and Huntington's diseases, but not in Parkinson's disease, we have shown the presence of misframed proteins such as misframed ubiquitin (UBB(+1)) of which we have determined the functional relevance in vitro and in vivo.Misframed proteins are the result of the inaccurate transcription of monotonic sequences in the genome and their subsequent translation. This process has been called 'molecular misreading'. In the present review, we will discuss the present state of the art with regard to UBB(+1) and amyloid precursor protein APP(+1).
散发性阿尔茨海默病和帕金森病是最常见的形式。与亨廷顿病一起,它们属于所谓的“构象疾病”,因为它们在不溶性蛋白质沉积物的积累方面具有共同的特征。在这篇综述中,我们重点介绍了泛素-蛋白酶体系统在构象疾病中的意义以及异常蛋白积累可能带来的后果。在所有形式的阿尔茨海默病和亨廷顿病中,但在帕金森病中没有,我们已经发现了异常蛋白质的存在,如异常的泛素(UBB(+1)),我们已经确定了其在体外和体内的功能相关性。异常蛋白质是基因组中单调序列转录不准确和随后翻译的结果。这个过程被称为“分子误读”。在本综述中,我们将讨论 UBB(+1) 和淀粉样前体蛋白 APP(+1) 的最新研究进展。