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Principles of MicroRNA–Target Recognition

机译:MicroRNA原理–目标识别

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摘要

MicroRNAs (miRNAs) are short non-coding RNAs that regulate gene expression in plants and animals. Although their biological importance has become clear, how they recognize and regulate target genes remains less well understood. Here, we systematically evaluate the minimal requirements for functional miRNA–target duplexes in vivo and distinguish classes of target sites with different functional properties. Target sites can be grouped into two broad categories. 5′ dominant sites have sufficient complementarity to the miRNA 5′ end to function with little or no support from pairing to the miRNA 3′ end. Indeed, sites with 3′ pairing below the random noise level are functional given a strong 5′ end. In contrast, 3′ compensatory sites have insufficient 5′ pairing and require strong 3′ pairing for function. We present examples and genome-wide statistical support to show that both classes of sites are used in biologically relevant genes. We provide evidence that an average miRNA has approximately 100 target sites, indicating that miRNAs regulate a large fraction of protein-coding genes and that miRNA 3′ ends are key determinants of target specificity within miRNA families.
机译:微小RNA(miRNA)是短的非编码RNA,可调节植物和动物中的基因表达。尽管它们的生物学重要性已变得很清楚,但如何识别和调节靶基因仍知之甚少。在这里,我们系统地评估了体内功能性miRNA-靶标双链体的最低要求,并区分了具有不同功能特性的靶标位点类别。目标站点可以分为两大类。 5'显性位点与miRNA 5'末端具有足够的互补性,几乎没有与miRNA 3'末端配对的功能。实际上,在强噪声5'端的情况下,具有低于随机噪声水平3'配对的位点是有效的。相反,3'补偿位点的5'配对不足,需要强力的3'配对才能发挥作用。我们提供示例和全基因组统计支持,以证明这两种类型的位点都用于生物学相关的基因。我们提供的证据表明,平均miRNA具有大约100个靶位点,表明miRNA调节了大部分蛋白质编码基因,而miRNA 3'末端是miRNA家族内靶标特异性的关键决定因素。

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