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首页> 外文期刊>Nucleic acids research >PAREameters: a tool for computational inference of plant miRNA–mRNA targeting rules using small RNA and degradome sequencing data
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PAREameters: a tool for computational inference of plant miRNA–mRNA targeting rules using small RNA and degradome sequencing data

机译:分段计:使用小RNA和降低测量测序数据的植物miRNA-mRNA靶向规则的计算推理的工具

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MicroRNAs (miRNAs) are short, non-coding RNAs that modulate the translation-rate of messenger RNAs (mRNAs) by directing the RNA-induced silencing complex to sequence-specific targets. In plants, this typically results in cleavage and subsequent degradation of the mRNA. Degradome sequencing is a high-throughput technique developed to capture cleaved mRNA fragments and thus can be used to support miRNA target prediction. The current criteria used for miRNA target prediction were inferred on a limited number of experimentally validated A.?thaliana interactions and were adapted to fit these specific interactions; thus, these fixed criteria may not be optimal across all datasets (organisms, tissues or treatments). We present a new tool, PAREameters, for inferring targeting criteria from small RNA and degradome sequencing datasets. We evaluate its performance using a more extensive set of experimentally validated interactions in multiple A. thaliana datasets. We also perform comprehensive analyses to highlight and quantify the differences between subsets of miRNA–mRNA interactions in model and non-model organisms. Our results show increased sensitivity in A. thaliana when using the PAREameters inferred criteria and that using data-driven criteria enables the identification of additional interactions that further our understanding of the RNA silencing pathway in both model and non-model organisms.
机译:MicroRNA(miRNA)是短的,非编码RNA,其通过将RNA诱导的沉默复合物指导到序列特异性靶标来调节信使RNA(MRNA)的翻译率。在植物中,这通常导致切割和随后的mRNA降解。降低测序是开发用于捕获切割的mRNA片段的高通量技术,因此可用于支持miRNA靶预测。在有限数量的实验验证的A.?Thaliana相互作用上推断出用于miRNA靶预测的目前标准,并适合适合这些特定的相互作用;因此,这些固定标准可能在所有数据集(生物,组织或治疗)上都不是最佳的。我们介绍了一个新的工具,分段计,用于推断来自小型RNA和降级测序数据集的靶向标准。我们使用多个A. Thaliana数据集中的更广泛的实验验证的交互来评估其性能。我们还进行全面的分析以突出显示和量化模型和非模型生物中miRNA-mRNA相互作用子集之间的差异。我们的结果表明,当使用剖钉表推断标准时,拟连座中的敏感性增加了,并且使用数据驱动标准使得能够鉴定额外的相互作用,进一步了解模型和非模型生物中的RNA沉默途径。

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