Kong Ping, Lei Ping, Zhang Shishuang, Li Dai, Zhao Jing, Zhang Benshu
Department of Geriatrics, Tianjin Medical University General Hospital,Tianjin Geriatrics Institute, China.
Department of Neurology, Tianjin Medical University General Hospital, China.
Neurosci Lett. 2018 Jan 1;662:51-58. doi: 10.1016/j.neulet.2017.09.051. Epub 2017 Sep 28.
Parkinson's disease (PD) is the second most common neurodegenerative disease and the exact pathogenic mechanism remains mostly elusive. Our study aims to identify the key differentially expressed genes (DEGs) and up regulators in PD.
An integrated analysis of microarray studies of PD was performed to identify the DEGs in PD compared to normal control (NC). Based on these DEGs, we performed the functional annotation and transcriptional regulatory network constructions. Q-RT-PCR was performed to verify the expression of DEGs.
Seven datasets were obtained from GEO. A total of 276 DEGs (262 up-regulated and 14 down-regulated DEGs) in PD compared to normal control were identified with selecting criteria of p-value<0.05. GO terms of respiratory electron transport chain, protein binding and cytoplasm were significantly enriched in PD. Pathways of oxidative phosphorylation, Parkinson's disease, Alzheimer's disease and Huntington's disease were significantly enriched in PD. SNCA was the hub protein in PD according to the protein-protein interaction (PPI) network. The top 3 transcription factor (TFs) covering the most downstream DEGs were Oct-1, Pax-4 and Evi-1. A total of 19 DEGs were firstly identified in our integrated analysis, not from the other individual datasets enrolled in this study.
Several DEGs including SNCA, COX17, COX4I1, COX7B, COX6A1 and ATP5J targeted by Pax-4, Oct-1 and Evi-1 may involve in the neurodegeneration and pathogenesis of PD by regulating oxidative phosphorylation, ATP production and oxidative stress, which was benefit for uncovering the mechanism of PD and developing new diagnostic and therapeutic strategies.
帕金森病(PD)是第二常见的神经退行性疾病,其确切的致病机制大多仍不清楚。我们的研究旨在识别帕金森病中关键的差异表达基因(DEG)和上调因子。
对帕金森病的微阵列研究进行综合分析,以识别与正常对照(NC)相比帕金森病中的DEG。基于这些DEG,我们进行了功能注释和转录调控网络构建。进行qRT-PCR以验证DEG的表达。
从GEO获得了七个数据集。以p值<0.05为选择标准,与正常对照相比,在帕金森病中总共鉴定出276个DEG(262个上调DEG和14个下调DEG)。呼吸电子传递链、蛋白质结合和细胞质的基因本体(GO)术语在帕金森病中显著富集。氧化磷酸化、帕金森病、阿尔茨海默病和亨廷顿病的信号通路在帕金森病中显著富集。根据蛋白质-蛋白质相互作用(PPI)网络,α-突触核蛋白(SNCA)是帕金森病中的枢纽蛋白。覆盖最下游DEG的前3个转录因子(TF)是八聚体转录因子1(Oct-1)、配对盒基因4(Pax-4)和Ecotropic病毒整合位点1(Evi-1)。在我们的综合分析中首次鉴定出总共19个DEG,而不是来自本研究中纳入的其他单个数据集。
由Pax-4、Oct-1和Evi-1靶向的几个DEG,包括SNCA、细胞色素c氧化酶17(COX17)、细胞色素c氧化酶亚基4I1(COX4I1)、细胞色素c氧化酶亚基7B(COX7B)、细胞色素c氧化酶亚基6A1(COX6A1)和ATP合酶F1偶联因子5J(ATP5J),可能通过调节氧化磷酸化、ATP生成和氧化应激参与帕金森病的神经退行性变和发病机制,这有助于揭示帕金森病的机制并制定新的诊断和治疗策略。