Departments of Structural Biology and Developmental Neurobiology and St. Jude Proteomics Facility, St. Jude Children's Research Hospital, Memphis, TN 38105.
Proc Natl Acad Sci U S A. 2013 Oct 8;110(41):16562-7. doi: 10.1073/pnas.1310249110. Epub 2013 Sep 10.
Deposition of insoluble protein aggregates is a hallmark of neurodegenerative diseases. The universal presence of β-amyloid and tau in Alzheimer's disease (AD) has facilitated advancement of the amyloid cascade and tau hypotheses that have dominated AD pathogenesis research and therapeutic development. However, the underlying etiology of the disease remains to be fully elucidated. Here we report a comprehensive study of the human brain-insoluble proteome in AD by mass spectrometry. We identify 4,216 proteins, among which 36 proteins accumulate in the disease, including U1-70K and other U1 small nuclear ribonucleoprotein (U1 snRNP) spliceosome components. Similar accumulations in mild cognitive impairment cases indicate that spliceosome changes occur in early stages of AD. Multiple U1 snRNP subunits form cytoplasmic tangle-like structures in AD but not in other examined neurodegenerative disorders, including Parkinson disease and frontotemporal lobar degeneration. Comparison of RNA from AD and control brains reveals dysregulated RNA processing with accumulation of unspliced RNA species in AD, including myc box-dependent-interacting protein 1, clusterin, and presenilin-1. U1-70K knockdown or antisense oligonucleotide inhibition of U1 snRNP increases the protein level of amyloid precursor protein. Thus, our results demonstrate unique U1 snRNP pathology and implicate abnormal RNA splicing in AD pathogenesis.
不溶性蛋白质聚集体的沉积是神经退行性疾病的一个标志。β-淀粉样蛋白和tau 在阿尔茨海默病(AD)中的普遍存在促进了淀粉样蛋白级联和tau 假说的发展,这些假说主导了 AD 发病机制研究和治疗开发。然而,该疾病的根本病因仍有待充分阐明。在这里,我们通过质谱法对 AD 患者的人脑不溶性蛋白质组进行了全面研究。我们鉴定出 4216 种蛋白质,其中 36 种蛋白质在疾病中积累,包括 U1-70K 和其他 U1 小核核糖核蛋白(U1 snRNP)剪接体成分。轻度认知障碍病例中的类似积累表明剪接体变化发生在 AD 的早期阶段。在 AD 中,但不在其他检查的神经退行性疾病(包括帕金森病和额颞叶痴呆)中,多种 U1 snRNP 亚基形成细胞质缠结样结构。AD 和对照大脑的 RNA 比较显示,AD 中存在 RNA 处理失调,未剪接的 RNA 物种积累,包括 myc 盒依赖性相互作用蛋白 1、载脂蛋白和早老素-1。U1-70K 敲低或 U1 snRNP 的反义寡核苷酸抑制增加了淀粉样前体蛋白的蛋白质水平。因此,我们的结果表明 U1 snRNP 具有独特的病理学,并暗示异常的 RNA 剪接与 AD 的发病机制有关。