Abstract

BackgroundCircular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures. Compared with the traditional linear RNA, circRNA is more stable and not easily degraded. Many studies have shown that circRNAs are involved in the regulation of various diseases and cancers. Determining the functions of circRNAs in mammalian cells is of great significance for revealing their mechanism of action in physiological and pathological processes, diagnosis and treatment of diseases. However, determining the functions of circRNAs on a large scale is a challenging task because of the high experimental costs.ResultsIn this paper, we present a hierarchical deep learning model, DeepciRGO, which can effectively predict gene ontology functions of circRNAs. We build a heterogeneous network containing circRNA co-expressions, protein–protein interactions and protein–circRNA interactions. The topology features of proteins and circRNAs are calculated using a novel representation learning approach HIN2Vec across the heterogeneous network. Then, a deep multi-label hierarchical classification model is trained with the topology features to predict the biological process function in the gene ontology for each circRNA. In particular, we manually curated a benchmark dataset containing 185 GO annotations for 62 circRNAs, namely, circRNA2GO-62. The DeepciRGO achieves promising performance on the circRNA2GO-62 dataset with a maximum F-measure of 0.412, a recall score of 0.400, and an accuracy of 0.425, which are significantly better than other state-of-the-art RNA function prediction methods. In addition, we demonstrate the considerable potential of integrating multiple interactions and association networks.ConclusionsDeepciRGO will be a useful tool for accurately annotating circRNAs. The experimental results show that integrating multi-source data can help to improve the predictive performance of DeepciRGO. Moreover, The model also can combine RNA structure and sequence information to further optimize predictive performance.

Highlights

  • IntroductionCircular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures

  • Circular RNAs are special noncoding RNA molecules with closed loop structures

  • All the results demonstrate that DeepciRGO, using HIN2Vec to extract the topology of the global network, can greatly improve the prediction performance of circRNA function

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Summary

Introduction

Circular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures. Determining the functions of circRNAs in mammalian cells is of great significance for revealing their mechanism of action in physiological and pathological processes, diagnosis and treatment of diseases. CircRNAs are rich in miRNA binding sites to act as miRNA sponges, preventing miRNA from interacting with mRNA in the 3′ non-translated region, and indirectly regulating the expression of downstream target miRNA genes. This mechanism is called competitive endogenous RNA (ceRNA) [5]. Determining the function of circRNAs in mammalian cells is of great significance for revealing the mechanism of action, diagnosis, and prevention of diseases in physiological and pathological processes

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