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Related Concept Videos

The Eukaryotic Promoter Region02:40

The Eukaryotic Promoter Region

The eukaryotic promoter region is a segment of DNA located upstream of a gene. It contains an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences.  The proximal promoter region is located in the vicinity of the gene and has cis-regulatory sequences and the core promoter. The core promoter is the binding site for RNA polymerase and is usually located between -35 and +35 nucleotides from the transcription start site. The distal promoter regions are...
The Eukaryotic Promoter Region02:40

The Eukaryotic Promoter Region

The eukaryotic promoter region is a segment of DNA located upstream of a gene. It contains an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences.  The proximal promoter region is located in the vicinity of the gene and has cis-regulatory sequences and the core promoter. The core promoter is the binding site for RNA polymerase and is usually located between -35 and +35 nucleotides from the transcription start site. The distal promoter regions are...

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Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions
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DistanceScan: a tool for promoter modeling.

Vladimir Shelest1, Daniela Albrecht, Ekaterina Shelest

  • 1Research group Systems Biology/Bioinformatics, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute, Beutenbergstr. 11a, 07745 Jena, Germany.

Bioinformatics (Oxford, England)
|April 3, 2010
PubMed
Summary

This study introduces a new R tool for promoter modeling in higher eukaryotes. It identifies functional combinations of transcription factor binding sites (TFBSs) by analyzing their distance distributions, improving promoter analysis.

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Area of Science:

  • Computational biology
  • Bioinformatics
  • Genomics

Background:

  • Current promoter modeling focuses on transcription factor binding site (TFBS) combinations rather than single sites.
  • Predicting functional TFBS combinations is crucial for understanding gene regulation in higher eukaryotes.

Purpose of the Study:

  • To develop and implement a novel computational tool for predicting functional TFBS pairs in eukaryotic promoters.
  • To enhance promoter modeling by filtering noise and identifying overrepresented TFBS combinations.

Main Methods:

  • Utilizes a previously developed method based on the distance distributions of TFBS pairs.
  • Models random distance distributions and compares them with observed distributions in query sequences.
  • Integrates with existing TFBS and motif prediction tools (Gibbs Sampler, Match, MEME/FIMO).

Main Results:

  • Identifies potentially functional TFBS combinations by filtering noise through profile comparison.
  • Outputs a list of predicted TFBS pairs with scores, P-values, and distribution plots.
  • The approach is validated as an effective filtering technique for promoter modeling.

Conclusions:

  • The developed R tool advances the state of the art in promoter modeling for higher eukaryotes.
  • The method effectively identifies overrepresented TFBS pairs, aiding in the discovery of functional regulatory elements.
  • The tool provides a valuable resource for researchers in computational biology and genomics.