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Related Concept Videos

Transcription Factors02:16

Transcription Factors

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Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
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Cooperative Binding of Transcription Regulators02:13

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Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
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General Transcription Factors01:30

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Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
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Eukaryotic Transcription Activators02:42

Eukaryotic Transcription Activators

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Transcription activators are proteins that promote the transcription of genes from DNA to RNA. In most cases, these proteins contain two separate domains ‒ a domain that binds to DNA and a domain for activating transcription; however, in some cases, a single domain is responsible for both binding and activation of transcription, as seen in the glucocorticoid receptor and MyoD.
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
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Combinatorial Gene Control02:33

Combinatorial Gene Control

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Combinatorial gene control is the synergistic action of several transcriptional factors to regulate the expression of a single gene. The absence of one or more of these factors may lead to a significant difference in the level of gene expression or repression.
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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.
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GraphTGI: an attention-based graph embedding model for predicting TF-target gene interactions.

Zhi-Hua Du1, Yang-Han Wu1, Yu-An Huang1

  • 1College of Computer Science and Software Engineering, ShenZhen University, 3688 Nanhai Avenue, Shenzhen, China.

Briefings in Bioinformatics
|May 5, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces GraphTGI, a novel deep learning model for predicting transcription factor (TF)-target gene interactions. GraphTGI effectively identifies these crucial biological relationships by analyzing known interactions and gene features.

Keywords:
chemical similaritygraph auto-encodergraph neural networktranscription factortranscriptional regulatory network

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Transcription factor (TF)-target gene interactions are fundamental to transcriptional regulation.
  • Current computational methods primarily focus on predicting TF binding sites, not direct interactions.
  • Biological techniques for identifying TF-target interactions are limited.

Purpose of the Study:

  • To develop a computational model for predicting TF-target gene interactions.
  • To address the limitations of existing methods by directly predicting interactions.
  • To leverage known interaction networks and gene features for improved prediction.

Main Methods:

  • Formulated TF-target gene interaction prediction as a link prediction problem on a knowledge graph.
  • Developed a deep learning model named GraphTGI.
  • GraphTGI utilizes a graph attention-based encoder and a bilinear decoder.

Main Results:

  • The GraphTGI model achieved an average AUC of 0.8864 +/- 0.0057 in 5-fold cross-validation.
  • Demonstrated outstanding performance in predicting TF-target gene interactions on a real dataset.
  • The model effectively learns patterns from known TF-target gene interactions.

Conclusions:

  • GraphTGI is the first model to predict TF-target gene interactions by learning patterns from known networks.
  • The model offers an effective and efficient approach for large-scale TF-target gene interaction prediction.
  • The developed model advances the field of transcriptional regulation research.