Center for non-coding RNA in Technology and Health, University of Copenhagen, Frederiksberg C, Denmark.
Bioinformatics. 2011 Jan 15;27(2):211-9. doi: 10.1093/bioinformatics/btq634. Epub 2010 Nov 18.
Predicting RNA-RNA interactions is essential for determining the function of putative non-coding RNAs. Existing methods for the prediction of interactions are all based on single sequences. Since comparative methods have already been useful in RNA structure determination, we assume that conserved RNA-RNA interactions also imply conserved function. Of these, we further assume that a non-negligible amount of the existing RNA-RNA interactions have also acquired compensating base changes throughout evolution. We implement a method, PETcofold, that can take covariance information in intra-molecular and inter-molecular base pairs into account to predict interactions and secondary structures of two multiple alignments of RNA sequences.
PETcofold's ability to predict RNA-RNA interactions was evaluated on a carefully curated dataset of 32 bacterial small RNAs and their targets, which was manually extracted from the literature. For evaluation of both RNA-RNA interaction and structure prediction, we were able to extract only a few high-quality examples: one vertebrate small nucleolar RNA and four bacterial small RNAs. For these we show that the prediction can be improved by our comparative approach. Furthermore, PETcofold was evaluated on controlled data with phylogenetically simulated sequences enriched for covariance patterns at the interaction sites. We observed increased performance with increased amounts of covariance.
The program PETcofold is available as source code and can be downloaded from http://rth.dk/resources/petcofold.
预测 RNA-RNA 相互作用对于确定假定的非编码 RNA 的功能至关重要。现有的相互作用预测方法都是基于单个序列的。由于比较方法在 RNA 结构确定方面已经很有用,我们假设保守的 RNA-RNA 相互作用也暗示着保守的功能。在这些相互作用中,我们进一步假设,相当数量的现有 RNA-RNA 相互作用在进化过程中也已经获得了补偿碱基变化。我们实现了一种方法 PETcofold,它可以考虑分子内和分子间碱基对的协方差信息,以预测两个 RNA 序列的多重比对的相互作用和二级结构。
我们在一个经过精心整理的数据集上评估了 PETcofold 预测 RNA-RNA 相互作用的能力,该数据集由 32 个细菌小 RNA 及其靶标组成,这些小 RNA 及其靶标是从文献中手动提取的。为了评估 RNA-RNA 相互作用和结构预测,我们只能提取出少数高质量的例子:一个脊椎动物小核仁 RNA 和四个细菌小 RNA。对于这些例子,我们表明我们的比较方法可以提高预测的准确性。此外,我们还在具有相互作用位点协方差模式的系统发育模拟序列富集的受控数据上评估了 PETcofold。我们观察到随着协方差的增加,性能得到了提高。
PETcofold 程序作为源代码提供,可以从 http://rth.dk/resources/petcofold 下载。