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首页> 外文期刊>Nature structural & molecular biology >Desperately seeking microRNA targets
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Desperately seeking microRNA targets

机译:拼命寻找microRNA靶标

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摘要

MicroRNAs (miRNAs) suppress gene expression by inhibiting translation, promoting mRNA decay or both. Each miRNA may regulate hundreds of genes to control the cell's response to developmental and other environmental cues. The best way to understand the function of a miRNA is to identify the genes that it regulates. Target gene identification is challenging because miRNAs bind to their target mRNAs by partial complementarity over a short sequence, suppression of an individual target gene is often small, and the rules of targeting are not completely understood. Here we review computational and experimental approaches to the identification of miRNA-regulated genes. The examination of changes in gene expression that occur when miRNA expression is altered and biochemical isolation of miRNA-associated transcripts complement target prediction algorithms. Bioinformatic analysis of over-represented pathways and nodes in protein-DNA interactomes formed from experimental candidate miRNA gene target lists can focus attention on biologically significant target genes.
机译:MicroRNA(miRNA)通过抑制翻译,促进mRNA衰减或同时抑制两者来抑制基因表达。每个miRNA可能调节数百个基因,以控制细胞对发育和其他环境线索的反应。了解miRNA功能的最好方法是鉴定其调控的基因。靶基因的鉴定具有挑战性,因为miRNA通过短序列的部分互补性与其靶mRNA结合,单个靶基因的抑制作用通常很小,并且靶向规则尚不完全清楚。在这里,我们回顾了miRNA调控基因鉴定的计算和实验方法。当miRNA表达改变且与miRNA相关的转录本的生化分离可补充靶标预测算法时,检查基因表达的变化。由实验候选miRNA基因靶标列表形成的蛋白质-DNA相互作用组中过度表达的途径和节点的生物信息学分析可以将注意力集中在具有生物学意义的靶标基因上。

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