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Related Concept Videos

Conserved Binding Sites01:49

Conserved Binding Sites

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Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
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Related Experiment Video

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A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells
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EnContact: predicting enhancer-enhancer contacts using sequence-based deep learning model.

Mingxin Gan1, Wenran Li2,3,4, Rui Jiang2

  • 1Donlinks School of Economics and Management, University of Science and Technology Beijing, Beijing, China.

Peerj
|October 1, 2019
PubMed
Summary
This summary is machine-generated.

We developed EnContact, a deep learning model that predicts enhancer-enhancer (E-E) contacts from genomic sequences. This method advances understanding of gene regulation and disease by exploring previously uncharacterized E-E interactions.

Keywords:
Attention-based RNNDeep learningEnhancer-enhancer contactsHiChIP dataHub enhancers

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Area of Science:

  • Genomics
  • Computational Biology
  • Molecular Biology

Background:

  • Chromatin contacts between regulatory elements are vital for gene transcription and disease mechanisms.
  • Current computational tools primarily predict enhancer-promoter interactions, neglecting enhancer-enhancer (E-E) contacts.

Purpose of the Study:

  • To introduce EnContact, a novel deep learning model for predicting E-E contacts using genomic sequences.
  • To evaluate EnContact's predictive performance and compare it against existing methods.

Main Methods:

  • Developed a deep learning model (EnContact) that utilizes genomic sequences for E-E contact prediction.
  • Validated the model using HiChIP data from seven cell lines.
  • Compared EnContact's performance against baseline computational methods.

Main Results:

  • EnContact demonstrated statistically significant predictive ability for E-E contacts.
  • The model outperformed existing baseline methods in predicting E-E interactions.
  • EnContact identified finer-mapping E-E interactions and a class of active 'hub enhancers' across cell lines.

Conclusions:

  • EnContact effectively predicts E-E interactions by learning features directly from genomic sequences.
  • The model enhances the exploration of E-E contacts, contributing to a deeper understanding of transcriptional regulation and disease.
  • Identified hub enhancers suggest their broad regulatory roles across different cell types.