snoRNAs are Deregulated in Patients with Parkinson’s Disease

P. Tokgün, A. Tomatır, Fatma Gizem Sarıekiz, Sinan Bi̇r
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Abstract

Purpose: Small nucleolar RNAs are ranging from 65 to 300 nucleotides in length that mediate post-transcriptional RNA modifications. They don’t have a 5′-Cap and a poly-A tail and are categorized as C/D box snoRNAs, H/ACA box snoRNAs, and small Cajal body-specific RNAs. snoRNAs have essential roles in important biological processes such as transcription, RNA splicing, cell cycle, and etc. In this study, we tried to reveal differential expressions of snoRNAs in PBMCs of patients with Parkinson’s Disease by microarray analysis. Materials and methods: Patients (n=3) who are considered to have a unilateral onset history and a good response to dopaminergic treatment in the first years were included in the study. 10 ml peripheral blood sample was taken for peripheral blood mononuclear cell isolation. Total RNA was extracted using GeneAll® Hybrid-R™ kit and microarray analysis was performed by using Affymetrix GeneChip Human ST 2.0 platform. Raw data were extracted using Affymetrix Command Console Software 1.1. KEGG pathway and GO terms analyses were performed and protein-protein interaction of host genes were determined by using STRING database. Results: Data from patients revealed that there were 28 snoRNAs were downregulated and 3 snoRNAs were upregulated. Conclusion: Here in this study, we evaluated the differential expressions of snoRNAs in patients with a definitive diagnosis of PD by microarray analysis and observed deregulated expressions of some snoRNAs. Differential expression of snoRNA may cause changes in the transcriptional activity of host genes and thus can serve as biomarkers for diseases.
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帕金森病患者的snorna失调
目的:小核仁RNA的长度在65到300个核苷酸之间,介导转录后RNA修饰。它们没有5 ' -Cap和poly-A尾部,被归类为C/D盒状snoRNAs, H/ACA盒状snoRNAs和小型Cajal体特异性rna。snoRNAs在转录、RNA剪接、细胞周期等重要生物学过程中发挥着重要作用。在本研究中,我们试图通过微阵列分析揭示帕金森病患者外周血单核细胞中snorna的差异表达。材料和方法:被认为有单侧发病史且在第一年对多巴胺能治疗反应良好的患者(n=3)被纳入研究。取外周血10 ml进行外周血单个核细胞分离。使用GeneAll®Hybrid-R™试剂盒提取总RNA,使用Affymetrix GeneChip Human ST 2.0平台进行微阵列分析。使用Affymetrix Command Console Software 1.1提取原始数据。对KEGG通路和GO术语进行分析,并利用STRING数据库确定宿主基因的蛋白相互作用。结果:患者数据显示,有28个snoRNAs下调,3个snoRNAs上调。结论:在本研究中,我们通过微阵列分析评估了明确诊断为PD的患者中snoRNAs的差异表达,并观察到一些snoRNAs的表达失调。snoRNA的差异表达可能引起宿主基因转录活性的改变,因此可以作为疾病的生物标志物。
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