Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.

Predicting RNA-binding protein (RBP) specificity is important for understanding gene expression regulation and RNA-mediated enzymatic processes. It is widely believed that RBP binding specificity is determined by both the sequence and structural contexts of RNAs. Existing approaches, including tradi...

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Main Authors: Yufeng Su, Yunan Luo, Xiaoming Zhao, Yang Liu, Jian Peng
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-09-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007283
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spelling doaj-762af1eb1e9a478da68736c9f88edd252021-04-21T15:10:18ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-09-01159e100728310.1371/journal.pcbi.1007283Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.Yufeng SuYunan LuoXiaoming ZhaoYang LiuJian PengPredicting RNA-binding protein (RBP) specificity is important for understanding gene expression regulation and RNA-mediated enzymatic processes. It is widely believed that RBP binding specificity is determined by both the sequence and structural contexts of RNAs. Existing approaches, including traditional machine learning algorithms and more recently, deep learning models, have been extensively applied to integrate RNA sequence and its predicted or experimental RNA structural probabilities for improving the accuracy of RBP binding prediction. Such models were trained mostly on the large-scale in vitro datasets, such as the RNAcompete dataset. However, in RNAcompete, most synthetic RNAs are unstructured, which makes machine learning methods not effectively extract RBP-binding structural preferences. Furthermore, RNA structure may be variable or multi-modal according to both theoretical and experimental evidence. In this work, we propose ThermoNet, a thermodynamic prediction model by integrating a new sequence-embedding convolutional neural network model over a thermodynamic ensemble of RNA secondary structures. First, the sequence-embedding convolutional neural network generalizes the existing k-mer based methods by jointly learning convolutional filters and k-mer embeddings to represent RNA sequence contexts. Second, the thermodynamic average of deep-learning predictions is able to explore structural variability and improves the prediction, especially for the structured RNAs. Extensive experiments demonstrate that our method significantly outperforms existing approaches, including RCK, DeepBind and several other recent state-of-the-art methods for predictions on both in vitro and in vivo data. The implementation of ThermoNet is available at https://github.com/suyufeng/ThermoNet.https://doi.org/10.1371/journal.pcbi.1007283
collection DOAJ
language English
format Article
sources DOAJ
author Yufeng Su
Yunan Luo
Xiaoming Zhao
Yang Liu
Jian Peng
spellingShingle Yufeng Su
Yunan Luo
Xiaoming Zhao
Yang Liu
Jian Peng
Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
PLoS Computational Biology
author_facet Yufeng Su
Yunan Luo
Xiaoming Zhao
Yang Liu
Jian Peng
author_sort Yufeng Su
title Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
title_short Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
title_full Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
title_fullStr Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
title_full_unstemmed Integrating thermodynamic and sequence contexts improves protein-RNA binding prediction.
title_sort integrating thermodynamic and sequence contexts improves protein-rna binding prediction.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-09-01
description Predicting RNA-binding protein (RBP) specificity is important for understanding gene expression regulation and RNA-mediated enzymatic processes. It is widely believed that RBP binding specificity is determined by both the sequence and structural contexts of RNAs. Existing approaches, including traditional machine learning algorithms and more recently, deep learning models, have been extensively applied to integrate RNA sequence and its predicted or experimental RNA structural probabilities for improving the accuracy of RBP binding prediction. Such models were trained mostly on the large-scale in vitro datasets, such as the RNAcompete dataset. However, in RNAcompete, most synthetic RNAs are unstructured, which makes machine learning methods not effectively extract RBP-binding structural preferences. Furthermore, RNA structure may be variable or multi-modal according to both theoretical and experimental evidence. In this work, we propose ThermoNet, a thermodynamic prediction model by integrating a new sequence-embedding convolutional neural network model over a thermodynamic ensemble of RNA secondary structures. First, the sequence-embedding convolutional neural network generalizes the existing k-mer based methods by jointly learning convolutional filters and k-mer embeddings to represent RNA sequence contexts. Second, the thermodynamic average of deep-learning predictions is able to explore structural variability and improves the prediction, especially for the structured RNAs. Extensive experiments demonstrate that our method significantly outperforms existing approaches, including RCK, DeepBind and several other recent state-of-the-art methods for predictions on both in vitro and in vivo data. The implementation of ThermoNet is available at https://github.com/suyufeng/ThermoNet.
url https://doi.org/10.1371/journal.pcbi.1007283
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