4.5 Article

An explainable artificial intelligence approach for decoding the enhancer histone modifications code and identification of novel enhancers in Drosophila

期刊

GENOME BIOLOGY
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-021-02532-7

关键词

Enhancers; Histone modifications; Explainable Artificial Intelligence; Gene regulation; Drosophila

资金

  1. University of Essex
  2. Wellcome Trust [202012/Z/16/Z]
  3. Queen Mary University of London
  4. Wellcome Trust [202012/Z/16/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

By using machine learning and explainable artificial intelligence model, the location of known enhancers in Drosophila can be predicted accurately, providing insight into the underlying histone modifications code. A large set of putative enhancers with similar epigenetic signature as known enhancers were identified, showing intermediate enrichment of mediator and cohesin complexes. 10-15% of predicted enhancers display characteristics similar to super enhancers observed in other species.
Background Enhancers are non-coding regions of the genome that control the activity of target genes. Recent efforts to identify active enhancers experimentally and in silico have proven effective. While these tools can predict the locations of enhancers with a high degree of accuracy, the mechanisms underpinning the activity of enhancers are often unclear. Results Using machine learning (ML) and a rule-based explainable artificial intelligence (XAI) model, we demonstrate that we can predict the location of known enhancers in Drosophila with a high degree of accuracy. Most importantly, we use the rules of the XAI model to provide insight into the underlying combinatorial histone modifications code of enhancers. In addition, we identified a large set of putative enhancers that display the same epigenetic signature as enhancers identified experimentally. These putative enhancers are enriched in nascent transcription, divergent transcription and have 3D contacts with promoters of transcribed genes. However, they display only intermediary enrichment of mediator and cohesin complexes compared to previously characterised active enhancers. We also found that 10-15% of the predicted enhancers display similar characteristics to super enhancers observed in other species. Conclusions Here, we applied an explainable AI model to predict enhancers with high accuracy. Most importantly, we identified that different combinations of epigenetic marks characterise different groups of enhancers. Finally, we discovered a large set of putative enhancers which display similar characteristics with previously characterised active enhancers.

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