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Tissue Non-Specific Genes and Pathways Associated with Diabetes: An Expression Meta-Analysis

机译:组织非特异性基因和糖尿病相关途径:表达Meta分析。

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摘要

We performed expression studies to identify tissue non-specific genes and pathways of diabetes by meta-analysis. We searched curated datasets of the Gene Expression Omnibus (GEO) database and identified 13 and five expression studies of diabetes and insulin responses at various tissues, respectively. We tested differential gene expression by empirical Bayes-based linear method and investigated gene set expression association by knowledge-based enrichment analysis. Meta-analysis by different methods was applied to identify tissue non-specific genes and gene sets. We also proposed pathway mapping analysis to infer functions of the identified gene sets, and correlation and independent analysis to evaluate expression association profile of genes and gene sets between studies and tissues. Our analysis showed that PGRMC1 and HADH genes were significant over diabetes studies, while IRS1 and MPST genes were significant over insulin response studies, and joint analysis showed that HADH and MPST genes were significant over all combined data sets. The pathway analysis identified six significant gene sets over all studies. The KEGG pathway mapping indicated that the significant gene sets are related to diabetes pathogenesis. The results also presented that 12.8% and 59.0% pairwise studies had significantly correlated expression association for genes and gene sets, respectively; moreover, 12.8% pairwise studies had independent expression association for genes, but no studies were observed significantly different for expression association of gene sets. Our analysis indicated that there are both tissue specific and non-specific genes and pathways associated with diabetes pathogenesis. Compared to the gene expression, pathway association tends to be tissue non-specific, and a common pathway influencing diabetes development is activated through different genes at different tissues.
机译:我们进行了表达研究,以通过荟萃分析确定组织非特异性基因和糖尿病的途径。我们搜索了基因表达综合(GEO)数据库的精选数据集,并分别确定了13种和5种在各种组织中糖尿病和胰岛素反应的表达研究。我们通过基于经验贝叶斯的线性方法测试了差异基因的表达,并通过基于知识的富集分析研究了基因集表达的关联。应用不同方法进行荟萃分析,以鉴定组织非特异性基因和基因集。我们还提出了通路图谱分析以推断已鉴定基因集的功能,并进行相关和独立分析以评估研究与组织之间基因和基因集的表达关联概况。我们的分析表明,PGRMC1和HADH基因在糖尿病研究中具有重要意义,而IRS1和MPST基因在胰岛素反应研究中具有重要意义,联合分析表明,在所有组合数据集中,HADH和MPST基因均具有显着意义。通路分析在所有研究中确定了六个重要的基因集。 KEGG通路图谱表明重要的基因集与糖尿病的发病机理有关。结果还表明,成对研究分别有12.8%和59.0%与基因和基因组的表达相关性显着相关。此外,有12.8%的成对研究具有独立的基因表达关联,但没有观察到基因集表达关联的显着差异。我们的分析表明,既有组织特异性基因又有非特异性基因和途径与糖尿病的发病机理有关。与基因表达相比,途径关联倾向于是组织非特异性的,并且通过不同组织的不同基因激活影响糖尿病发展的常见途径。

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