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Cooperative gene regulation by microRNA pairs and their identification using a computational workflow

机译:通过microRNA对进行协同基因调控并使用计算流程进行鉴定

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MicroRNAs (miRNAs) are an integral part of gene regulation at the post-transcriptional level. Recently, it has been shown that pairs of miRNAs can repress the translation of a target mRNA in a cooperative manner, which leads to an enhanced effectiveness and specificity in target repression. However, it remains unclear which miRNA pairs can synergize and which genes are target of cooperative miRNA regulation. In this paper, we present a computational workflow for the prediction and analysis of cooperating miRNAs and their mutual target genes, which we refer to as RNA triplexes. The workflow integrates methods of miRNA target prediction; triplex structure analysis; molecular dynamics simulations and mathematical modeling for a reliable prediction of functional RNA triplexes and target repression efficiency. In a case study we analyzed the human genome and identified several thousand targets of cooperative gene regulation. Our results suggest that miRNA cooperativity is a frequent mechanism for an enhanced target repression by pairs of miRNAs facilitating distinctive and fine-tuned target gene expression patterns. Human RNA triplexes predicted and characterized in this study are organized in a web resource at www.sbi.uni-rostock.de/triplexrna/
机译:MicroRNA(miRNA)在转录后水平是基因调控的组成部分。最近,已显示成对的miRNA可以协同方式抑制靶mRNA的翻译,这导致靶抑制的效力和特异性增强。但是,尚不清楚哪些miRNA对可以协同作用,哪些基因是协同miRNA调控的靶标。在本文中,我们介绍了用于预测和分析协同miRNA及其相互靶基因的计算工作流程,我们将其称为RNA三元体。该工作流程整合了miRNA靶标预测方法;三重结构分析;分子动力学模拟和数学建模可可靠预测功能性RNA三链体和靶标抑制效率。在一个案例研究中,我们分析了人类基因组并确定了数千个合作基因调控的靶标。我们的结果表明,miRNA的协同作用是通过成对的miRNA促进独特的和微调的靶基因表达模式对靶标抑制作用增强的常见机制。这项研究中预测和表征的人类RNA三链体在www.sbi.uni-rostock.de/triplexrna/网站上的网络资源中进行了组织。

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