Abstract

MicroRNAs (miRNAs) are small, non-coding RNA molecules that regulate gene expression in almost all plants and animals. They play an important role in key processes, such as proliferation, apoptosis, and pathogen–host interactions. Nevertheless, the mechanisms by which miRNAs act are not fully understood. The first step toward unraveling the function of a particular miRNA is the identification of its direct targets. This step has shown to be quite challenging in animals primarily because of incomplete complementarities between miRNA and target mRNAs. In recent years, the use of machine-learning techniques has greatly increased the prediction of miRNA targets, avoiding the need for costly and time-consuming experiments to achieve miRNA targets experimentally. Among the most important machine-learning algorithms are decision trees, which classify data based on extracted rules. In the present work, we used a genetic algorithm in combination with C4.5 decision tree for prediction of miRNA targets. We applied our proposed method to a validated human datasets. We nearly achieved 93.9% accuracy of classification, which could be related to the selection of best rules.

Highlights

  • MicroRNAs are known as single-stranded non-coding RNAs ranging in length from 19 to 25 nucleotides

  • We introduce an efficient genetic algorithm-based decision tree to select the best rules among all extracted rule sets which leads to improve the accuracy of prediction

  • We introduce a genetic algorithm, which works as follows: Upon extracting rules, N classification rules are extracted in the form of ‘‘if . . . . . .” where N is total of rules in rule sets

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Summary

Introduction

MicroRNAs (miRNAs) are known as single-stranded non-coding RNAs ranging in length from 19 to 25 nucleotides (nt). A large number of miRNAs are evolutionarily conserved across species boundaries [1]. MiRNA are uncapped, unpolyadenylated small RNAs, which are transcribed by RNA polymerase II into long primary transcripts (pri-miRNAs) [2,3]. The primary transcripts are processed to mature miRNA in sequential steps by the RNase III endonucleases Drosha in the nucleus [4] and Dicer in the cytoplasm [5]. The mature miRNA is incorporated into an RNA molecule, which induces a silencing complex (RISC) and guides RISC to complementary mRNA targets.

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