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miRTCat: a comprehensive map of human and mouse microRNA target sites including non-canonical nucleation bulges

机译:miRTCat:人和小鼠microRNA目标位点的全面图谱,包括非典型成核凸起

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摘要

MicroRNAs (miRNAs) regulate various biological functions by binding hundreds of transcripts to impart post-transcriptional repression. Recently, by applying a transcriptome-wide experimental method for identifying miRNA target sites (Ago HITS-CLIP), a novel non-canonical target site, named 'nucleation bulge', was discovered as widespread, functional and evolutionally conserved. Although such non-canonical nucleation bulges have been proven to be predictive by using 'pivot pairing rule' and sequence conservation, this approach has not been applied yet. To facilitate the functional studies of non-canonical miRNA targets, we implement miRTCat: a comprehensive searchable map of miRNA target sites, including non-canonical nucleation bulges, not only mapped in experimentally verified miRNA-bound regions but also predicted in all 30-untranslated regions (30-UTRs) derived from human and mouse (similar to 15.6% as expected false-positive results).
机译:MicroRNA(miRNA)通过结合数百种转录物来赋予转录后抑制,从而调节各种生物学功能。最近,通过应用转录组范围的实验方法鉴定miRNA靶位点(Ago HITS-CLIP),发现了一种新的非经典靶位点,称为“成核凸起”,具有广泛的功能和进化上的保守性。尽管已通过使用“枢轴配对规则”和序列保守性证明了此类非规范成核凸起是可预测的,但该方法尚未应用。为了促进非经典miRNA靶标的功能研究,我们实施了miRTCat:miRNA目标位点的全面可搜索图谱,包括非经典成核凸起,不仅映射在经过实验验证的miRNA结合区域中,而且还预测了所有30个未翻译的来自人和小鼠的区域(30-UTR)(与预期的假阳性结果相近15.6%)。

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