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Biological features between miRNAs and their targets are unveiled from deep learning models
MicroRNAs (miRNAs) are ~ 22 nucleotide ubiquitous gene regulators. They modulate a broad range of essential cellular processes linked to human health and diseases. Consequently, identifying miRNA targets and understanding how they function are critical for treating miRNA associated diseases. In our...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664955/ https://www.ncbi.nlm.nih.gov/pubmed/34893648 http://dx.doi.org/10.1038/s41598-021-03215-w |
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author | Gu, Tongjun Xie, Mingyi Barbazuk, W. Brad Lee, Ji-Hyun |
author_facet | Gu, Tongjun Xie, Mingyi Barbazuk, W. Brad Lee, Ji-Hyun |
author_sort | Gu, Tongjun |
collection | PubMed |
description | MicroRNAs (miRNAs) are ~ 22 nucleotide ubiquitous gene regulators. They modulate a broad range of essential cellular processes linked to human health and diseases. Consequently, identifying miRNA targets and understanding how they function are critical for treating miRNA associated diseases. In our earlier work, a hybrid deep learning-based approach (miTAR) was developed for predicting miRNA targets. It performs substantially better than the existing methods. The approach integrates two major types of deep learning algorithms: convolutional neural networks (CNNs) and recurrent neural networks (RNNs). However, the features in miRNA:target interactions learned by miTAR have not been investigated. In the current study, we demonstrated that miTAR captures known features, including the involvement of seed region and the free energy, as well as multiple novel features, in the miRNA:target interactions. Interestingly, the CNN and RNN layers of the model perform differently at capturing the free energy feature: the units in RNN layer is more unique at capturing the feature but collectively the CNN layer is more efficient at capturing the feature. Although deep learning models are commonly thought “black-boxes”, our discoveries support that the biological features in miRNA:target can be unveiled from deep learning models, which will be beneficial to the understanding of the mechanisms in miRNA:target interactions. |
format | Online Article Text |
id | pubmed-8664955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86649552021-12-15 Biological features between miRNAs and their targets are unveiled from deep learning models Gu, Tongjun Xie, Mingyi Barbazuk, W. Brad Lee, Ji-Hyun Sci Rep Article MicroRNAs (miRNAs) are ~ 22 nucleotide ubiquitous gene regulators. They modulate a broad range of essential cellular processes linked to human health and diseases. Consequently, identifying miRNA targets and understanding how they function are critical for treating miRNA associated diseases. In our earlier work, a hybrid deep learning-based approach (miTAR) was developed for predicting miRNA targets. It performs substantially better than the existing methods. The approach integrates two major types of deep learning algorithms: convolutional neural networks (CNNs) and recurrent neural networks (RNNs). However, the features in miRNA:target interactions learned by miTAR have not been investigated. In the current study, we demonstrated that miTAR captures known features, including the involvement of seed region and the free energy, as well as multiple novel features, in the miRNA:target interactions. Interestingly, the CNN and RNN layers of the model perform differently at capturing the free energy feature: the units in RNN layer is more unique at capturing the feature but collectively the CNN layer is more efficient at capturing the feature. Although deep learning models are commonly thought “black-boxes”, our discoveries support that the biological features in miRNA:target can be unveiled from deep learning models, which will be beneficial to the understanding of the mechanisms in miRNA:target interactions. Nature Publishing Group UK 2021-12-10 /pmc/articles/PMC8664955/ /pubmed/34893648 http://dx.doi.org/10.1038/s41598-021-03215-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gu, Tongjun Xie, Mingyi Barbazuk, W. Brad Lee, Ji-Hyun Biological features between miRNAs and their targets are unveiled from deep learning models |
title | Biological features between miRNAs and their targets are unveiled from deep learning models |
title_full | Biological features between miRNAs and their targets are unveiled from deep learning models |
title_fullStr | Biological features between miRNAs and their targets are unveiled from deep learning models |
title_full_unstemmed | Biological features between miRNAs and their targets are unveiled from deep learning models |
title_short | Biological features between miRNAs and their targets are unveiled from deep learning models |
title_sort | biological features between mirnas and their targets are unveiled from deep learning models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664955/ https://www.ncbi.nlm.nih.gov/pubmed/34893648 http://dx.doi.org/10.1038/s41598-021-03215-w |
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