Evidence map›Paper›PMID 39227799›Full record

ArticleBMC genomics2024

Predicting splicing patterns from the transcription factor binding sites in the promoter with deep learning.

Tzu-Chieh Lin, Cheng-Hung Tsai, Cheng-Kai Shiau, Jia-Hsin Huang, Huai-Kuang Tsai

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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tzu-Chieh Lin *Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
Cheng-Hung Tsai *Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
Cheng-Kai ShiauInstitute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
Jia-Hsin HuangInstitute of Information Science, Academia Sinica, Taipei, 11529, Taiwan. jiahsin.huang@gmail.com.
Huai-Kuang TsaiInstitute of Information Science, Academia Sinica, Taipei, 11529, Taiwan. hktsai@iis.sinica.edu.tw.ORCID http://orcid.org/0000-0002-4200-8137

Funding

Academia Sinica AS-GC-110-L15National Science and Technology Council 108-2221-E-001-014-MY3National Science and Technology Council 110-2221-E-001-013-MY3
6 · The paper itself

Abstract

backgroundAlternative splicing is a pivotal mechanism of post-transcriptional modification that contributes to the transcriptome plasticity and proteome diversity in metazoan cells. Although many splicing regulations around the exon/intron regions are known, the relationship between promoter-bound transcription factors and the downstream alternative splicing largely remains unexplored.

resultsIn this study, we present computational approaches to unravel the regulatory relationship between promoter-bound transcription factor binding sites (TFBSs) and the splicing patterns. We curated a fine dataset that includes DNase I hypersensitive site sequencing and transcriptomes across fifteen human tissues from ENCODE. Specifically, we proposed different representations of TF binding context and splicing patterns to examine the associations between the promoter and downstream splicing events. While machine learning models demonstrated potential in predicting splicing patterns based on TFBS occupancies, the limitations in the generalization of predicting the splicing forms of singleton genes across diverse tissues was observed with carefully examination using different cross-validation methods. We further investigated the association between alterations in individual TFBS at promoters and shifts in exon splicing efficiency. Our results demonstrate that the convolutional neural network (CNN) models, trained on TF binding changes in the promoters, can predict the changes in splicing patterns. Furthermore, a systemic in silico substitutions analysis on the CNN models highlighted several potential splicing regulators. Notably, using empirical validation using K562 CTCFL shRNA knock-down data, we showed the significant role of CTCFL in splicing regulation.

conclusionIn conclusion, our finding highlights the potential role of promoter-bound TFBSs in influencing the regulation of downstream splicing patterns and provides insights for discovering alternative splicing regulations.

Indexed as

Alternative SplicingDeep LearningPromoter Regions, GeneticTranscription FactorsBinding SitesComputational BiologyExonsHumansTranscription FactorsAlternative splicingCNNDeep learningTFBSTranscriptional regulation

Identifiers

PMID39227799
PMCPMC11373144

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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.