基于RNA二级结构的3D图形表示的微小RNA预测。

Turkish journal of biology = Turk biyoloji dergisi Pub Date : 2019-08-05 eCollection Date: 2019-01-01 DOI:10.3906/biy-1904-59
Müşerref Duygu Saçar Demirci
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引用次数: 4

摘要

微小RNA(miRNA)是基因表达的转录后调节因子。虽然一个miRNA可以靶向数百个信使RNA,但一个mRNA可以被不同的miRNA靶向,更不用说单个miRNA在mRNA序列中可能具有不同的结合位点。因此,对miRNA进行实验研究是非常有意义的。因此,机器学习(ML)经常被用来克服这些挑战。ML分析的关键部分在很大程度上取决于输入数据的质量和描述数据的特征的能力。此前,miRNA有1000多个特征被提出。这里,表明使用36个表示RNA二级结构的特征及其动态3D图形表示提供了高达98%的准确度值。在这项研究中,提出了一种基于ML的miRNA预测的新方法。通过使用3个分类器对已知的人类miRNA和假发夹进行分类,生成了数千个模型:决策树、朴素贝叶斯和随机森林。尽管该方法基于人类数据,但最好的模型能够正确分配MirGeneDB中96%的非人发夹,这表明该方法可能对分析其他物种的miRNA有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MicroRNA prediction based on 3D graphical representation of RNA secondary structures.

MicroRNA prediction based on 3D graphical representation of RNA secondary structures.

MicroRNA prediction based on 3D graphical representation of RNA secondary structures.

MicroRNA prediction based on 3D graphical representation of RNA secondary structures.

MicroRNAs (miRNAs) are posttranscriptional regulators of gene expression. While a miRNA can target hundreds of messenger RNA (mRNAs), an mRNA can be targeted by different miRNAs, not to mention that a single miRNA might have various binding sites in an mRNA sequence. Therefore, it is quite involved to investigate miRNAs experimentally. Thus, machine learning (ML) is frequently used to overcome such challenges. The key parts of a ML analysis largely depend on the quality of input data and the capacity of the features describing the data. Previously, more than 1000 features were suggested for miRNAs. Here, it is shown that using 36 features representing the RNA secondary structure and its dynamic 3D graphical representation provides up to 98% accuracy values. In this study, a new approach for ML-based miRNA prediction is proposed. Thousands of models are generated through classification of known human miRNAs and pseudohairpins with 3 classifiers: decision tree, naïve Bayes, and random forest. Although the method is based on human data, the best model was able to correctly assign 96% of nonhuman hairpins from MirGeneDB, suggesting that this approach might be useful for the analysis of miRNAs from other species.

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