Lin D, Liang Y, Jing X, Chen Y, Lei M, Zeng Z, Zhou T, Wu X, Peng S, Zheng D, Huang K, Yang L, Xiao S, Liu J, Tao E
Department of Neurology, The Sun Yat-sen Memorial Hospital of Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou 510080, China.
Department of Neurology, The Sun Yat-sen Memorial Hospital of Sun Yat-sen University, 107 Yanjiang West Road, Guangzhou 510080, China; Guangdong Province Key Laboratory of Brain Function and Disease, Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou 510080, China.
Brain Res. 2018 Jan 1;1678:384-396. doi: 10.1016/j.brainres.2017.11.007. Epub 2017 Nov 12.
Long non-coding RNAs (lncRNAs) are a new research focus that are reported to influence the pathogenetic process of neurodegenerative disorders. To uncover new disease-associated genes and their relevant mechanisms, we carried out a gene microarray analysis based on a Parkinson's disease (PD) in vitro model induced by α-synuclein oligomers. This cellular model induced by 25 μmol/L α-synuclein oligomers has been confirmed to show the stable, transmissible neurotoxicity of α-synuclein, a typical PD pathological marker. And several differentially expressed lncRNAs and mRNAs were identified in this model, such as G046036, G030771, AC009365.4, RPS14P3, CTB-11I22.1, and G007549. Subsequent ceRNA analysis determined the potential relationships between these lncRNAs and their associated mRNAs and microRNAs. The results of the present study widen our horizon of PD susceptibility genes and provide new pathways towards efficient diagnostic biomarkers and therapeutic targets for PD.
长链非编码RNA(lncRNAs)是一个新的研究热点,据报道其会影响神经退行性疾病的发病过程。为了发现新的疾病相关基因及其相关机制,我们基于由α-突触核蛋白寡聚体诱导的帕金森病(PD)体外模型进行了基因芯片分析。由25μmol/Lα-突触核蛋白寡聚体诱导的这种细胞模型已被证实表现出α-突触核蛋白稳定、可传播的神经毒性,α-突触核蛋白是一种典型的PD病理标志物。并且在该模型中鉴定出了几种差异表达的lncRNAs和mRNAs,如G046036、G030771、AC009365.4、RPS14P3、CTB-11I22.1和G007549。随后的ceRNA分析确定了这些lncRNAs与其相关的mRNAs和微小RNAs之间的潜在关系。本研究结果拓宽了我们对PD易感基因的认识,并为PD的有效诊断生物标志物和治疗靶点提供了新途径。