Gene expression profiling predicts pathways and genes associated with Parkinson’s disease

被引:0
作者
Shuang Liu
Yong Zhang
Hong Bian
Xiaohong Li
机构
[1] Jinan Central Hospital Affiliated to Shandong University,Department of Neurology
来源
Neurological Sciences | 2016年 / 37卷
关键词
Parkinson’s disease; Differentially expressed genes; Pathway enrichment analysis; Protein–protein interaction network; Hub protein;
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学科分类号
摘要
This study was aimed to explore the molecular mechanism of Parkinson’s disease (PD) development and discover underlying pathways and genes associated with PD. The microarray data of GSE22491 containing 10 samples from PD patients and 8 samples from healthy controls (HC) were downloaded from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) were identified by paired t-test. Then the DEGs were performed cluster and principal component analyses followed by Gene Ontology (GO) and pathway enrichment analyses and protein–protein interaction (PPI) network construction. Total 176 up-regulated DEGs and 49 down-regulated DEGs were identified. Totally, 39 GO terms and 72 pathways were closely related to PD. Pathway of neuronal system was enriched by 10 DEGs such as synapsin I (SYN1), glutamate receptor, ionotropic, N-methyl-d-aspartate 1 (GRIN1) and GRIN2D. In the PPI networks, 18 hub genes were obtained, such as GRIN2D and discs, large (Drosophila) homolog-associated protein 3 (DLGAP3). The pathway of neuronal system and its enriched DEGs may play important roles in PD progression. The DEGs such as SYN1, GRIN1, GRIN2D and DLGAP3 may become promising candidate genes for PD.
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页码:73 / 79
页数:6
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共 221 条
[31]  
Kieburtz K(2007) and Aging Cell 6 267-9573
[32]  
Marshall F(1999) polymorphisms and Parkinson’s disease in a hospital-based case–control study Trends Pharmacol Sci 20 46-16691
[33]  
Ravina B(2008)Localization of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13. 1–qter, the NMDAR2A subunit gene to 16p13. 2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24–q25 using somatic cell hybrid and radiation hybrid mapping panels Neurology 70 1438-293
[34]  
Schifitto G(2011)Cellular interplay between neurons and glia: toward a comprehensive mechanism for excitotoxic neuronal loss in neurodegeneration J Neurosci 31 9563-214
[35]  
Siderowf A(2011)Metabotropic glutamate receptor subtype 4 selectively modulates both glutamate and GABA transmission in the striatum: implications for Parkinson’s disease treatment J Neurosci 31 16685-87
[36]  
Greenamyre JT(2011)Amino acids as dietary excitotoxins: a contribution to understanding neurodegenerative disorders Nat Neurosci 14 285-187
[37]  
Hastings TG(2010)The importance of being subtle: small changes in calcium homeostasis control cognitive decline in normal aging Curr Neurol Neurosci Rep 10 207-1304
[38]  
Azzouz M(2013)Neuronal cell death: a demise with different shapes Psychiatry Res 208 84-396
[39]  
Martin-Rendon E(2011)Use of antihypertensives and the risk of Parkinson disease Compr Psychiatry 52 181-undefined
[40]  
Barber RD(2002)Sapap3 deletion anomalously activates short-term endocannabinoid-mediated synaptic plasticity Lancet 360 1302-undefined