首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Transcriptomic profiling of differentially expressed genes and related pathways in different brain regions in Parkinson's disease
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Transcriptomic profiling of differentially expressed genes and related pathways in different brain regions in Parkinson's disease

机译:帕金森病不同脑区中差异表达基因及相关途径的转录组分析

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摘要

Parkinson's disease (PD) is the second most common neurodegenerative disease. However, the expression pattern and the differential gene in different brain regions and its functions remain unclear although many studies have been reported. In this present study, PD mouse model were build and four brain regions (cerebral cortex: CC, hippocampus: HP, striatum: ST, and cerebellum: CB) were separated for RNA-seq analysis. Results showed that different expressed genes were found between the different brain regions and more differential genes found in ST and HP when compared with control groups. Among them, Lrrk2, Mtor, Gxylt1, C920006o11Rik, Vdac1, Drd4, and Ncan showed the most significant to PD. PDCC vs. PDHP, PDHP vs. PDST and PDCC vs. PDST groups have 334, 722 and 495 differentially expressed genes (DEGs), respectively. Functional analyses results showed that the differential genes mainly related with posttranscriptional regulation of gene expression and protein localization to organelle and so on, which involved in AMPK, PI3K-Akt signaling pathway, and GABA-ergic synapse. Network biology analysis showed LRRK2, DRD2, IGF-1, GNAI1, GNAI3, PRKACA, PPP2R5C, and PIK3R1 play a major role in protein regulation of PD. Therefore, HP and ST play more important roles in the development of PD and it is also suggested the potential target gene for diagnosis and treatment of PD.
机译:帕金森病(PD)是第二种最常见的神经变性疾病。然而,尽管许多研究已经报道的表达模式,并在不同的脑区和其功能的基因差异仍不清楚。在此研究中,PD小鼠模型的构建和脑区(大脑皮层:CC,海马:HP,纹状体:ST,和小脑:CB)分离用于RNA-SEQ分析。结果表明,发现不同的大脑区域更差之间的基因差异表达的基因在ST和惠普发现与对照组相比。其中,LRRK2,MTOR,Gxylt1,C920006o11Rik,VDAC1,DRD4和NCAN显示出PD最显著。 PDCC与PDHP,PDHP与PDST和PDCC与PDST组有334,分别722和495个差异表达基因(DEGS)。功能分析结果表明,该差异基因主要是与基因表达和蛋白定位的转录后调节到细胞器等,其中涉及在AMPK,PI3K-Akt信号传导途径,和GABA能突触相关。网络生物学分析表明,LRRK2,DRD2,IGF-1,GNAI1,GNAI3,PRKACA,PPP2R5C和PIK3R1起到PD的蛋白质调节中起主要作用。因此,惠普和ST在PD的发展中扮演更重要的角色,它也建议PD的诊断和治疗的潜在靶基因。

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