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Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network

BACKGROUND: Piwi-interacting RNAs (piRNAs) are the small non-coding RNAs (ncRNAs) that silence genomic transposable elements. And researchers found out that piRNA also regulates various endogenous transcripts. However, there is no systematic understanding of the piRNA binding patterns and how piRNA...

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Autores principales: Yang, Tzu-Hsien, Shiue, Sheng-Cian, Chen, Kuan-Yu, Tseng, Yan-Yuan, Wu, Wei-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520261/
https://www.ncbi.nlm.nih.gov/pubmed/34656087
http://dx.doi.org/10.1186/s12859-021-04428-6
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author Yang, Tzu-Hsien
Shiue, Sheng-Cian
Chen, Kuan-Yu
Tseng, Yan-Yuan
Wu, Wei-Sheng
author_facet Yang, Tzu-Hsien
Shiue, Sheng-Cian
Chen, Kuan-Yu
Tseng, Yan-Yuan
Wu, Wei-Sheng
author_sort Yang, Tzu-Hsien
collection PubMed
description BACKGROUND: Piwi-interacting RNAs (piRNAs) are the small non-coding RNAs (ncRNAs) that silence genomic transposable elements. And researchers found out that piRNA also regulates various endogenous transcripts. However, there is no systematic understanding of the piRNA binding patterns and how piRNA targets genes. While various prediction methods have been developed for other similar ncRNAs (e.g., miRNAs), piRNA holds distinctive characteristics and requires its own computational model for binding target prediction. RESULTS: Recently, transcriptome-wide piRNA binding events in C. elegans were probed by PRG-1 CLASH experiments. Based on the probed piRNA-messenger RNAs (mRNAs) binding pairs, in this research, we devised the first deep learning architecture based on multi-head attention to computationally identify piRNA targeting mRNA sites. In the devised deep network, the given piRNA and mRNA segment sequences are first one-hot encoded and undergo a combined operation of convolution and squeezing-extraction to unravel motif patterns. And we incorporate a novel multi-head attention sub-network to extract the hidden piRNA binding rules that can simulate the biological piRNA target recognition process. Finally, the true piRNA–mRNA binding pairs are identified by a deep fully connected sub-network. Our model obtains a supreme discriminatory power of AUC [Formula: see text] 93.3% on an independent test set and successfully extracts the verified binding pattern of a synthetic piRNA. These results demonstrated that the devised model achieves high prediction performance and suggests testable potential biological piRNA binding rules. CONCLUSIONS: In this research, we developed the first deep learning method to identify piRNA targeting sites on C. elegans mRNAs. And the developed deep learning method is demonstrated to be of high accuracy and can provide biological insights into piRNA–mRNA binding patterns. The piRNA binding target identification network can be downloaded from http://cosbi2.ee.ncku.edu.tw/data_download/piRNA_mRNA_binding.
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spelling pubmed-85202612021-10-20 Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network Yang, Tzu-Hsien Shiue, Sheng-Cian Chen, Kuan-Yu Tseng, Yan-Yuan Wu, Wei-Sheng BMC Bioinformatics Methodology Article BACKGROUND: Piwi-interacting RNAs (piRNAs) are the small non-coding RNAs (ncRNAs) that silence genomic transposable elements. And researchers found out that piRNA also regulates various endogenous transcripts. However, there is no systematic understanding of the piRNA binding patterns and how piRNA targets genes. While various prediction methods have been developed for other similar ncRNAs (e.g., miRNAs), piRNA holds distinctive characteristics and requires its own computational model for binding target prediction. RESULTS: Recently, transcriptome-wide piRNA binding events in C. elegans were probed by PRG-1 CLASH experiments. Based on the probed piRNA-messenger RNAs (mRNAs) binding pairs, in this research, we devised the first deep learning architecture based on multi-head attention to computationally identify piRNA targeting mRNA sites. In the devised deep network, the given piRNA and mRNA segment sequences are first one-hot encoded and undergo a combined operation of convolution and squeezing-extraction to unravel motif patterns. And we incorporate a novel multi-head attention sub-network to extract the hidden piRNA binding rules that can simulate the biological piRNA target recognition process. Finally, the true piRNA–mRNA binding pairs are identified by a deep fully connected sub-network. Our model obtains a supreme discriminatory power of AUC [Formula: see text] 93.3% on an independent test set and successfully extracts the verified binding pattern of a synthetic piRNA. These results demonstrated that the devised model achieves high prediction performance and suggests testable potential biological piRNA binding rules. CONCLUSIONS: In this research, we developed the first deep learning method to identify piRNA targeting sites on C. elegans mRNAs. And the developed deep learning method is demonstrated to be of high accuracy and can provide biological insights into piRNA–mRNA binding patterns. The piRNA binding target identification network can be downloaded from http://cosbi2.ee.ncku.edu.tw/data_download/piRNA_mRNA_binding. BioMed Central 2021-10-16 /pmc/articles/PMC8520261/ /pubmed/34656087 http://dx.doi.org/10.1186/s12859-021-04428-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Yang, Tzu-Hsien
Shiue, Sheng-Cian
Chen, Kuan-Yu
Tseng, Yan-Yuan
Wu, Wei-Sheng
Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title_full Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title_fullStr Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title_full_unstemmed Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title_short Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention network
title_sort identifying pirna targets on mrnas in c. elegans using a deep multi-head attention network
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520261/
https://www.ncbi.nlm.nih.gov/pubmed/34656087
http://dx.doi.org/10.1186/s12859-021-04428-6
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