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The Novel Regulatory Role of lncRNA-miRNA-mRNA Axis in Amyotrophic Lateral Sclerosis: An Integrated Bioinformatics Analysis

机译:LNCRNA-miRNA-mRNA轴在肌营养侧面硬化症中的新调节作用:综合生物信息学分析

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Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease that primarily affects motor neurons, causing muscle atrophy, bulbar palsy, and pyramidal tract signs. However, the aetiology and pathogenesis of ALS have not been elucidated to date. In this study, a competitive endogenous RNA (ceRNA) network was constructed by analyzing the expression profiles of messenger RNAs (mRNAs) and long noncoding RNAs (lncRNAs) that were matched by 7 ALS samples and 4 control samples, and then a protein-protein interaction (PPI) network was constructed to identify the genes related to ALS. Gene Ontology (GO) was used to study the potential functions of differentially expressed mRNAs (DEmRNAs) in the ceRNA network. For the ALS and control groups, 247177 potential lncRNA-mRNA ceRNA relationship pairs were screened. Analysis of significant relationship pairs demonstrated that the PPI modules formed by the MALAT1 -regulated SYNRG , ITSN2 , PICALM , AP3B1 , and AAK1 genes may play important roles in the pathogenesis of ALS, and these results may help to characterize the pathogenesis of ALS.
机译:肌萎缩的外侧硬化症(ALS)是一种治愈的神经退行性疾病,主要影响运动神经元,导致肌肉萎缩,凸起麻痹和金字塔迹象。然而,迄今为止,ALS的病因和发病机制尚未阐明。在该研究中,通过分析由7个Als样品和4个对照样品匹配的信使RNA(MRNA)和长的非编码RNA(LNCRNA)的表达谱来构建竞争性内源性RNA(CERNA)网络,然后是蛋白质 - 蛋白质构建相互作用(PPI)网络以识别与ALS相关的基因。基因本体(GO)用于研究差异表达MRNA(DEMRNA)在CERNA网络中的潜在功能。对于ALS和对照组,筛选了247177个潜在的LNCRNA-mRNA Cerna关系对。显着关系对的分析证明,Malat1 -Regulated Synrg,ITSN2,麦克白,AP3B1和AAK1基因形成的PPI模块可能在ALS的发病机制中起重要作用,并且这些结果可能有助于表征ALS的发病机制。

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