Related Experiment Video
Updated: Jun 22, 2026

08:54
In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression
Published on: March 29, 2019
Toward a gold standard for promoter prediction evaluation
Thomas Abeel1, Yves Van de Peer, Yvan Saeys
1Department of Plant Systems Biology, VIB, Ghent University, Gent, Belgium.
Bioinformatics (Oxford, England)
|May 30, 2009
Summary
This study introduces a standardized evaluation strategy for promoter prediction programs (PPPs). The new benchmark assesses 17 PPPs, offering a gold standard for future comparisons in genome annotation.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Promoter prediction is crucial for genome annotation, yet lacks standardized evaluation methods.
- Existing promoter prediction programs (PPPs) are often inadequately compared using limited genomic data.
- A unified evaluation design is needed for robust comparison of PPPs.
Purpose of the Study:
- To develop a large-scale benchmarking study for evaluating promoter prediction programs (PPPs).
- To propose a multi-faceted evaluation strategy serving as a gold standard for promoter prediction.
- To compare the performance of 17 state-of-the-art PPPs using the proposed strategy.
Main Methods:
- Conducted a large-scale benchmark of 17 state-of-the-art promoter prediction programs (PPPs).
- Developed and applied a multi-faceted evaluation strategy for promoter prediction.
- Analyzed predictive performance, promoter class specificity, predictor overlap, and positional bias.
Main Results:
- Presented a comprehensive comparison of 17 promoter prediction programs.
- Established a novel evaluation strategy for promoter prediction, suitable as a gold standard.
- Detailed analysis revealed insights into predictor performance, specificity, overlap, and bias.
Conclusions:
- The proposed evaluation strategy provides a robust framework for comparing promoter prediction tools.
- This benchmarking study offers valuable insights into the capabilities of current promoter prediction programs.
- The study facilitates more accurate and reliable genome annotation through improved promoter prediction evaluation.
Related Concept Videos
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 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...
Transcription Initiation
Initiation is the first step of transcription in eukaryotes. Prokaryotic RNA Polymerase (RNAP) can bind to the template DNA and start transcribing. On the other hand, transcription in eukaryotes requires additional proteins, called transcription factors, to first bind to the promoter region in the DNA template. This binding helps recruit the specific RNAP that can assemble on the DNA and start transcription.
The promoters and enhancers and their accessory proteins allow tight regulation of...
The promoters and enhancers and their accessory proteins allow tight regulation of...
Improving Translational Accuracy
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Improving Translational Accuracy
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
General Transcription Factors
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...

