Abstract
BackgroundMammalian genomes encode for thousands of microRNAs, which can potentially regulate the majority of protein-coding genes. They have been implicated in development and disease, leading to great interest in understanding their function, with computational methods being widely used to predict their targets. Most computational methods rely on sequence features, thermodynamics, and conservation filters; essentially scanning the whole transcriptome to predict one set of targets for each microRNA. This has the limitation of not considering that the same microRNA could have different sets of targets, and thus different functions, when expressed in different types of cells.ResultsTo address this problem, we combine popular target prediction methods with expression profiles, via machine learning, to produce a new predictor: TargetExpress. Using independent data from microarrays and high-throughput sequencing, we show that TargetExpress outperforms existing methods, and that our predictions are enriched in functions that are coherent with the added expression profile and literature reports.ConclusionsOur method should be particularly useful for anyone studying the functions and targets of miRNAs in specific tissues or cells. TargetExpress is available at: http://targetexpress.ceiabreulab.org/.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-2695-1) contains supplementary material, which is available to authorized users.
Highlights
Mammalian genomes encode for thousands of microRNAs, which can potentially regulate the majority of protein-coding genes
We applied our model to predict targets for hsa-miR29 in two different tissues: heart and brain. We selected this micro RNA (miRNA) because it is highly expressed in several adult tissues; we focus on these two particular tissues, since they have very different gene expression profiles
Training a Support Vector Machine We developed a Machine Learning classification model (TargetExpress) to improve available miRNA target predictions by including expression profiles
Summary
Mammalian genomes encode for thousands of microRNAs, which can potentially regulate the majority of protein-coding genes They have been implicated in development and disease, leading to great interest in understanding their function, with computational methods being widely used to predict their targets. Most computational methods rely on sequence features, thermodynamics, and conservation filters; essentially scanning the whole transcriptome to predict one set of targets for each microRNA. This has the limitation of not considering that the same microRNA could have different sets of targets, and different functions, when expressed in different types of cells. MicroRNAs (miRNAs) are small non-coding RNAs that guide Argonaute proteins to post-transcriptionally repress target messenger RNAs (mRNAs) [1].
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