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Predicting splicing patterns from the transcription factor binding sites in the promoter with deep learning.
Lin, Tzu-Chieh; Tsai, Cheng-Hung; Shiau, Cheng-Kai; Huang, Jia-Hsin; Tsai, Huai-Kuang.
Afiliação
  • Lin TC; Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
  • Tsai CH; Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
  • Shiau CK; Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan.
  • Huang JH; Institute of Information Science, Academia Sinica, Taipei, 11529, Taiwan. jiahsin.huang@gmail.com.
  • Tsai HK; Taiwan AI Labs & Foundation, Taipei, 10351, Taiwan. jiahsin.huang@gmail.com.
BMC Genomics ; 25(Suppl 3): 830, 2024 Sep 03.
Article em En | MEDLINE | ID: mdl-39227799
ABSTRACT

BACKGROUND:

Alternative 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.

RESULTS:

In 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.

CONCLUSION:

In 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Regiões Promotoras Genéticas / Processamento Alternativo / Aprendizado Profundo Limite: Humans Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Regiões Promotoras Genéticas / Processamento Alternativo / Aprendizado Profundo Limite: Humans Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Taiwan
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