Functional microRNA targets in protein coding sequences

Bioinformatics (Oxford, England) - Tập 28 Số 6 - Trang 771-776 - 2012
Martin Reczko1, Manolis Maragkakis1, Panagiotis Alexiou1, Ivo Große1, Artemis G. Hatzigeorgiou1
11 Institute of Molecular Oncology, Biomedical Sciences Research Center ‘Alexander Fleming’, Vari, Greece, 2Synaptic Ltd, Heraklion, Greece, 3Institute of Computer Science, Martin Luther University Halle-Wittenberg, 06120 Halle, Germany and 4Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, 19104 Philadelphia, USA

Tóm tắt

Abstract

Motivation: Experimental evidence has accumulated showing that microRNA (miRNA) binding sites within protein coding sequences (CDSs) are functional in controlling gene expression.

Results: Here we report a computational analysis of such miRNA target sites, based on features extracted from existing mammalian high-throughput immunoprecipitation and sequencing data. The analysis is performed independently for the CDS and the 3′-untranslated regions (3′-UTRs) and reveals different sets of features and models for the two regions. The two models are combined into a novel computational model for miRNA target genes, DIANA-microT-CDS, which achieves higher sensitivity compared with other popular programs and the model that uses only the 3′-UTR target sites. Further analysis indicates that genes with shorter 3′-UTRs are preferentially targeted in the CDS, suggesting that evolutionary selection might favor additional sites on the CDS in cases where there is restricted space on the 3′-UTR.

Availability: The results of DIANA-microT-CDS are available at www.microrna.gr/microT-CDS

Contact:  [email protected]; [email protected]

Supplementary information:  Supplementary data are available at Bioinformatics online.

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