Evidence map›Paper›PMID 34656087›Full record

ArticleBMC bioinformatics2021

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

Tzu-Hsien Yang, Sheng-Cian Shiue, Kuan-Yu Chen, Yan-Yuan Tseng, Wei-Sheng Wu

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 16 citations in OpenAlex.

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  8. In Silico Study of piRNA Interactions with the SARS-CoV-2 Genome.International journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Tzu-Hsien YangDepartment of Information Management, National University of Kaohsiung, Kaohsiung, Taiwan.
Sheng-Cian ShiueDepartment of Electrical Engineering, National Cheng Kung University, Tainan, Taiwan.
Kuan-Yu ChenDepartment of Electrical Engineering, National Cheng Kung University, Tainan, Taiwan.
Yan-Yuan TsengCenter for Molecular Medicine and Genetics, Wayne State University, School of Medicine, Detroit, MI, USA.
Wei-Sheng WuDepartment of Electrical Engineering, National Cheng Kung University, Tainan, Taiwan. wessonwu@mail.ncku.edu.tw.
National Cheng Kung University · TWNational University of Kaohsiung · TWWayne State University · US

Funding

Ministry of Science and Technology, Taiwan MOST 107-2218-E-390-009-MY3Ministry of Science and Technology, Taiwan MOST 107-2221-E-006-225-MY3Ministry of Science and Technology, Taiwan MOST 108-2628-E-006-004-MY3Ministry of Science and Technology, Taiwan MOST 110-2221-E-006-198-MY3
6 · The paper itself

Abstract

backgroundPiwi-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.

resultsRecently, 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.

conclusionsIn 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 .

Indexed as

Caenorhabditis elegans ProteinsMicroRNAsAnimalsArgonaute ProteinsCaenorhabditis elegansDNA Transposable ElementsRNA, MessengerRNA, Small InterferingArgonaute ProteinsCaenorhabditis elegans ProteinsDNA Transposable ElementsMicroRNAsPRG-1 protein, C elegansRNA, MessengerRNA, Small InterferingCLASHDeep learningMulti-head attentionpiRNA

Identifiers

PMID34656087
PMCPMC8520261
OpenAlexW3206978724

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.