Protein Network Analysis to Prioritize Key Genes and Pathway for Stress-Mediated Neurodegeneration

Q3 Computer Science Open Bioinformatics Journal Pub Date : 2018-10-18 DOI:10.2174/1875036201811010240
N. Srivastava, B. Mishra, P. Srivastava
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引用次数: 3

Abstract

Oxidative Stress (OS) has been implicated in the pathophysiology of many neurodegenerative diseases. OS can cause cellular damage that results in cell death due to overproduction of reactive oxygen species (ROS) that may play the crucial role in the disease progression. An impaired mechanism in correlation with reduced expression of antioxidant proteins is the very common feature among most of the age-related disorders. Variousin-vitroandin-vivostudies suggest the major contribution of oxidative stress in neurodegeneration. Role of Nrf2 gene is well established as a neuroprotective gene especially in concern with stress-mediated neurodegeneration. Nrf2 is a bZIP transcription factor that forms the heterodimer with small Maf protein and transcription factor AP1 that regulates transcription by binding to ARE which coordinates the transcription of genes involved in phase II detoxification and an antioxidant defense that is used to protect the cell from oxidative stress.The currentinsilicostudy was attempted to prioritize key genes and pathway in stress-mediated neurodegeneration through network-based analysis.Protein-protein interaction network was constructed and analyzed using 63 Nrf2 regulating candidate genes obtained from NCBI database based on literature studies usingSTRING 10.0database andCytoscape v 3.6.0software plug-inNetwork Analyzer.Further, the functional enrichment analysis of identified gene was done usingPANTHER GENE ONTOLOGYsoftware and DAVID tool.Based on network topological parameter, TP53, JUN, MYC, NFE2L2, AKT1, PIK3CA & UBC were identified as the key gene in the network. Among them, TP53 gene was obtained as a super hub gene with the highest Betweenness Centrality (BC) and node degree. The functional enrichment analysis was done usingPANTHER GENE ONTOLOGYsoftware and DAVID tool reveals their significant role in neurotrophin signaling pathway, MAPK signaling pathway, cellular response to stress & in the regulation of stress.The network analysis will help in prioritizing genes in the pathway that helps in understanding the underlying mechanism of disease. Thus, further study on these genes and their biological mechanism and pathway may, therefore, provide a potential target for the treatment of stress-mediated neurodegeneration.
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蛋白质网络分析优先处理应激介导的神经变性关键基因和途径
氧化应激(OS)与许多神经退行性疾病的病理生理有关。由于活性氧(ROS)的过量产生,OS可引起细胞损伤,导致细胞死亡,而活性氧可能在疾病进展中起关键作用。在大多数年龄相关疾病中,与抗氧化蛋白表达减少相关的受损机制是非常常见的特征。各种体外和体内研究表明氧化应激在神经退行性变中的主要作用。Nrf2基因是一种神经保护基因,特别是在应激介导的神经退行性疾病中。Nrf2是一种bZIP转录因子,与小Maf蛋白和转录因子AP1形成异源二聚体,通过与ARE结合调节转录,ARE协调参与II期解毒和抗氧化防御的基因转录,用于保护细胞免受氧化应激。当前的硅研究试图通过基于网络的分析来优先考虑应激介导的神经退行性变的关键基因和途径。基于文献研究,利用ingstring 10.0数据库和cytoscape v 3.6.0软件plug-inNetwork Analyzer,从NCBI数据库中获得63个Nrf2调控候选基因,构建蛋白-蛋白互作网络并进行分析。利用panther gene ontology软件和DAVID工具对鉴定的基因进行功能富集分析。基于网络拓扑参数,确定了TP53、JUN、MYC、NFE2L2、AKT1、PIK3CA和UBC为网络中的关键基因。其中,TP53基因作为超级枢纽基因,BC和节点度最高。利用panther GENE ontology软件和DAVID工具进行功能富集分析,揭示了它们在神经营养因子信号通路、MAPK信号通路、细胞应激反应和应激调控中的重要作用。网络分析将有助于确定通路中基因的优先级,从而有助于理解疾病的潜在机制。因此,进一步研究这些基因及其生物学机制和通路可能为治疗应激介导的神经变性提供潜在的靶点。
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来源期刊
Open Bioinformatics Journal
Open Bioinformatics Journal Computer Science-Computer Science (miscellaneous)
CiteScore
2.40
自引率
0.00%
发文量
4
期刊介绍: The Open Bioinformatics Journal is an Open Access online journal, which publishes research articles, reviews/mini-reviews, letters, clinical trial studies and guest edited single topic issues in all areas of bioinformatics and computational biology. The coverage includes biomedicine, focusing on large data acquisition, analysis and curation, computational and statistical methods for the modeling and analysis of biological data, and descriptions of new algorithms and databases. The Open Bioinformatics Journal, a peer reviewed journal, is an important and reliable source of current information on the developments in the field. The emphasis will be on publishing quality articles rapidly and freely available worldwide.
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