利用NMFAS识别与人类疾病相关的关键生物学途径

Hao Guo, Yun-ping Zhu, Dong Li, F. He, Qi-jun Liu
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摘要

基因表达微阵列使我们能够同时测量数千个基因的基因表达水平。本研究构建非负矩阵因子化分析策略(NMFAS),通过利用途径隶属度信息从微阵列矩阵中提取途径表达矩阵,将其因子化为行向量和列向量的乘积,从而挖掘与各种疾病相关的潜在生物学途径。我们将行向量定义为途径活性,列向量定义为基因贡献权。通过比较两个不同样本组的通路活性,我们可以确定显著表达的通路。我们将这一策略应用于两种不同的情况:吸烟和2型糖尿病(DM2)。通过比较吸烟者和从不吸烟者之间的通路活性,我们发现了152个差异表达通路,包括已在文献中验证的通路,如“o -甘聚糖生物合成”和谷胱甘肽代谢”。我们还发现了与吸烟表型相关的重要基因,如NQO、HSPA1A、ALDH3A1。对于DM2的分析,我们的结果发现9条通路显著表达,包括“氧化磷酸化”和“mTOR信号通路”等典型通路,并发现CAPNS1、APP、COX7A1、COX7B等基因可能在DM2的细胞调控中发挥重要作用。总之,我们的策略可以有效地用于整合基因表达谱和生物学途径信息,以识别人类疾病的关键过程,并可以识别其他方法遗漏的基因途径。
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Using NMFAS to identify key biological pathways associated with human diseases
Gene expression microarray enables us to measure the gene expression levels for thousands of genes at the same time. Here, we constructed the non-negative matrix factorization analysis strategy (NMFAS) to dig the underlying biological pathways related with various diseases by factorizing the pathway expression matrix, which was extracted from microarray matrix using pathway membership information, into the product of row and column vectors. We defined row vector as the pathway activity and column vector as the gene contribution weight. Via comparing the pathway activity of two different sample groups, we can identify significantly expressed pathways. We applied this strategy on two different cases: smoking and type 2 diabetes (DM2). We found 152 differentially expressed pathways by the comparison of pathway activity between smoker and never smoker, including pathways that have been validated in literature, such as “O-Glycans biosynthesis” and “Glutathione metabolism”. We also found important genes related to smoking phenotype, such as NQO, HSPA1A, ALDH3A1. As for DM2 analysis, our results suggested 9 pathways were significantly expressed, including typical pathways like “Oxidative phosphorylation” and “mTOR signaling pathway”, and found genes like CAPNS1, APP, COX7A1, COX7B, which might play important roles in the cellular regulations of DM2. In conclusion, Our strategy can be efficiently used to integrate gene expression profiles and biological pathway information to identify the key processes underlying human disease and can identify gene pathways missed by alternative approaches.
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