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首页> 外文期刊>BioData Mining >MicroRNA-mediated regulation of target genes in several brain regions is correlated to both microRNA-targeting-specific promoter methylation and differential microRNA expression
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MicroRNA-mediated regulation of target genes in several brain regions is correlated to both microRNA-targeting-specific promoter methylation and differential microRNA expression

机译:MicroRNA介导的几个大脑区域的靶基因调控与microRNA靶向特异性启动子甲基化和差异性microRNA表达相关

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Background Public domain databases nowadays provide multiple layers of genome-wide data e.g., promoter methylation, mRNA expression, and miRNA expression and should enable integrative modeling of the mechanisms of regulation of gene expression. However, researches along this line were not frequently executed. Results Here, the public domain dataset of mRNA expression, microRNA (miRNA) expression and promoter methylation patterns in four regions, the frontal cortex, temporal cortex, pons and cerebellum, of human brain were sourced from the National Center for Biotechnology Informations gene expression omnibus, and reanalyzed computationally. A large number of miRNA-mediated regulation of target genes and miRNA-targeting-specific promoter methylation were identified in the six pairwise comparisons among the four brain regions. The miRNA-mediated regulation of target genes was found to be highly correlated with one or both of miRNA-targeting-specific promoter methylation and differential miRNA expression. Genes enriched for Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways that were related to brain function and/or development were found among the target genes of miRNAs whose differential expression patterns were highly correlated with the miRNA-mediated regulation of their target genes. Conclusions The combinatorial analysis of miRNA-mediated regulation of target genes, miRNA-targeting-specific promoter methylation and differential miRNA expression can help reveal the brain region-specific contributions of miRNAs to brain function and development.
机译:背景技术当今的公共领域数据库提供了全基因组数据的多层,例如,启动子甲基化,mRNA表达和miRNA表达,并且应该能够对基因表达的调节机制进行整合建模。但是,沿这方面的研究并不经常进行。结果在这里,人类大脑的额叶皮层,颞叶皮层,脑桥和小脑四个区域的mRNA表达,microRNA(miRNA)表达和启动子甲基化模式的公共领域数据集来自美国国家生物技术信息中心基因表达综合,并重新进行计算分析。在四个大脑区域的六个成对比较中,发现了许多miRNA介导的靶基因调控和miRNA靶向特异性启动子甲基化。发现miRNA介导的靶基因调控与miRNA靶向特异性启动子甲基化和差异miRNA表达之一或两者高度相关。在miRNA的靶基因中发现了丰富的基因,这些基因丰富了与大脑功能和/或发育有关的京都基因与基因组百科全书(KEGG)途径,其差异表达模式与miRNA介导的靶基因调控高度相关。结论对miRNA介导的靶基因调控,miRNA靶向特异性启动子甲基化和miRNA差异表达的组合分析可以帮助揭示miRNA对大脑功能和发育的大脑区域特异性贡献。

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