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Inference of Target Gene Regulation via miRNAs during Cell Senescence by Using the MiRaGE Server

机译:使用MiRaGE服务器推断细胞衰老期间通过miRNA调控靶基因

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miRNAs have recently been shown to play a key role in cell senescence, by downregulating target genes. Thus, inference of those miRNAs that critically downregulate target genes is important. However, inference of target gene regulation by miRNAs is difficult and is often achieved simply by investigating significant upregulation during cell senescence. Here, we inferred the regulation of target genes by miRNAs, using the recently developed MiRaGE server, together with the change in miRNA expression during fibroblast IMR90 cell senescence. We revealed that the simultaneous consideration of 2 criteria, the up(down)regulation and the down(up) regulatiion of target genes, yields more feasible miRNA, i.e., those that are most frequently reported to be down/upregulated and/or to possess biological backgrounds that induce cell senescence. Thus, when analyzing miRNAs that critically contribute to cell senescence, it is important to consider the level of target gene regulation, simultaneously with the change in miRNA expression.
机译:最近显示,miRNA通过下调靶基因在细胞衰老中发挥关键作用。因此,推断那些严重下调靶基因的miRNA很重要。然而,通过miRNA推断靶基因调控是困难的,并且通常可以通过研究细胞衰老过程中的显着上调来简单地实现。在这里,我们使用最近开发的MiRaGE服务器推断了miRNA对靶基因的调控,以及成纤维细胞IMR90细胞衰老过程中miRNA表达的变化。我们发现同时考虑两个标准,即靶基因的上(下)调节和下(上)调节,产生了更可行的miRNA,即最常被报道为下/上调和/或拥有的miRNA。诱导细胞衰老的生物学背景。因此,在分析对细胞衰老起关键作用的miRNA时,重要的是要同时考虑靶基因的调控水平和miRNA表达的变化。

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