cWords - systematic microRNA regulatory motif discovery from mRNA expression data.

Silence Pub Date : 2013-05-20 DOI:10.1186/1758-907X-4-2
Simon H Rasmussen, Anders Jacobsen, Anders Krogh
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引用次数: 31

Abstract

Background: Post-transcriptional regulation of gene expression by small RNAs and RNA binding proteins is of fundamental importance in development of complex organisms, and dysregulation of regulatory RNAs can influence onset, progression and potentially be target for treatment of many diseases. Post-transcriptional regulation by small RNAs is mediated through partial complementary binding to messenger RNAs leaving nucleotide signatures or motifs throughout the entire transcriptome. Computational methods for discovery and analysis of sequence motifs in high-throughput mRNA expression profiling experiments are becoming increasingly important tools for the identification of post-transcriptional regulatory motifs and the inference of the regulators and their targets.

Results: cWords is a method designed for regulatory motif discovery in differential case-control mRNA expression datasets. We have improved the algorithms and statistical methods of cWords, resulting in at least a factor 100 speed gain over the previous implementation. On a benchmark dataset of 19 microRNA (miRNA) perturbation experiments cWords showed equal or better performance than two comparable methods, miReduce and Sylamer. We have developed rigorous motif clustering and visualization that accompany the cWords analysis for more intuitive and effective data interpretation. To demonstrate the versatility of cWords we show that it can also be used for identification of potential siRNA off-target binding. Moreover, cWords analysis of an experiment profiling mRNAs bound by Argonaute ribonucleoprotein particles discovered endogenous miRNA binding motifs.

Conclusions: cWords is an unbiased, flexible and easy-to-use tool designed for regulatory motif discovery in differential case-control mRNA expression datasets. cWords is based on rigorous statistical methods that demonstrate comparable or better performance than other existing methods. Rich visualization of results promotes intuitive and efficient interpretation of data. cWords is available as a stand-alone Open Source program at Github https://github.com/simras/cWords and as a web-service at: http://servers.binf.ku.dk/cwords/.

Abstract Image

Abstract Image

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从mRNA表达数据中发现系统的microRNA调控基序。
背景:小RNA和RNA结合蛋白对基因表达的转录后调控在复杂生物体的发育中具有重要意义,而调控RNA的失调可以影响许多疾病的发生、进展,并可能成为治疗的靶点。小rna的转录后调控是通过与信使rna的部分互补结合介导的,在整个转录组中留下核苷酸特征或基序。在高通量mRNA表达谱实验中发现和分析序列基序的计算方法正成为鉴定转录后调控基序和推断调控因子及其靶标的重要工具。结果:cWords是一种在差异病例对照mRNA表达数据集中发现调控基序的方法。我们改进了cWords的算法和统计方法,使速度比以前的实现提高了至少100倍。在19个microRNA (miRNA)扰动实验的基准数据集上,cWords表现出与miReduce和Sylamer两种可比方法相同或更好的性能。我们已经开发了严格的基序聚类和可视化,以配合cWords分析更直观和有效的数据解释。为了证明cWords的多功能性,我们表明它也可以用于鉴定潜在的siRNA脱靶结合。此外,对Argonaute核糖核蛋白颗粒结合mrna的实验分析发现了内源性miRNA结合基序。结论:cWords是一个无偏见、灵活且易于使用的工具,用于在不同病例对照的mRNA表达数据集中发现调控基序。cWords基于严格的统计方法,证明了与其他现有方法相当或更好的性能。丰富的结果可视化促进直观和有效的数据解释。cWords作为一个独立的开源程序可以在Github https://github.com/simras/cWords上获得,也可以在http://servers.binf.ku.dk/cwords/上作为一个web服务获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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