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starBase: a database for exploring microRNA–mRNA interaction maps from Argonaute CLIP-Seq and Degradome-Seq data

机译:starBase:一个数据库,用于从Argonaute CLIP-Seq和Degradome-Seq数据中探索microRNA-mRNA相互作用图

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摘要

MicroRNAs (miRNAs) represent an important class of small non-coding RNAs (sRNAs) that regulate gene expression by targeting messenger RNAs. However, assigning miRNAs to their regulatory target genes remains technically challenging. Recently, high-throughput CLIP-Seq and degradome sequencing (Degradome-Seq) methods have been applied to identify the sites of Argonaute interaction and miRNA cleavage sites, respectively. In this study, we introduce a novel database, starBase (sRNA target Base), which we have developed to facilitate the comprehensive exploration of miRNA–target interaction maps from CLIP-Seq and Degradome-Seq data. The current version includes high-throughput sequencing data generated from 21 CLIP-Seq and 10 Degradome-Seq experiments from six organisms. By analyzing millions of mapped CLIP-Seq and Degradome-Seq reads, we identified ∼1 million Ago-binding clusters and ∼2 million cleaved target clusters in animals and plants, respectively. Analyses of these clusters, and of target sites predicted by 6 miRNA target prediction programs, resulted in our identification of approximately 400 000 and approximately 66 000 miRNA-target regulatory relationships from CLIP-Seq and Degradome-Seq data, respectively. Furthermore, two web servers were provided to discover novel miRNA target sites from CLIP-Seq and Degradome-Seq data. Our web implementation supports diverse query types and exploration of common targets, gene ontologies and pathways. The starBase is available at http://starbase.sysu.edu.cn/.
机译:MicroRNA(miRNA)代表一类重要的小型非编码RNA(sRNA),它们通过靶向信使RNA来调节基因表达。但是,将miRNA分配给其调控靶基因在技术上仍然具有挑战性。最近,高通量CLIP-Seq和降解组测序(Degradome-Seq)方法已用于分别鉴定Argonaute相互作用位点和miRNA裂解位点。在这项研究中,我们介绍了一个新颖的数据库starBase(sRNA靶标碱基),我们已开发该数据库来促进从CLIP-Seq和Degradome-Seq数据全面探索miRNA-靶标相互作用图。当前版本包括从六个生物体的21个CLIP-Seq和10个Degradome-Seq实验生成的高通量测序数据。通过分析数百万个映射的CLIP-Seq和Degradome-Seq读数,我们分别在动植物中鉴定了约100万个Ago结合簇和约200万个裂解的靶簇。对这些簇的分析以及由6个miRNA目标预测程序预测的目标位点的分析,导致我们分别从CLIP-Seq和Degradome-Seq数据中识别出约400 identification000和约66 000 miRNA-靶标调控关系。此外,提供了两个Web服务器,以从CLIP-Seq和Degradome-Seq数据中发现新的miRNA靶位点。我们的网络实施支持各种查询类型以及对共同目标,基因本体论和途径的探索。可从http://starbase.sysu.edu.cn/获得starBase。

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