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Related Concept Videos

Improving Translational Accuracy02:07

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 Accuracy02:07

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...
Initiation of Translation02:33

Initiation of Translation

Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
Initiation of Translation02:33

Initiation of Translation

Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
Ribosome Profiling02:24

Ribosome Profiling

Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
Leaky Scanning02:28

Leaky Scanning

During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R stands for...

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Related Experiment Video

Updated: Jun 22, 2026

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
08:23

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data

Published on: February 18, 2022

Representative transcript sets for evaluating a translational initiation sites predictor.

Jia Zeng1, Reda Alhajj, Douglas J Demetrick

  • 1Department of Computer Science, University of Calgary, Calgary, AB T2N 1N4, Canada. jzeng@ucalgary.ca

BMC Bioinformatics
|July 4, 2009
PubMed
Summary
This summary is machine-generated.

We developed a new algorithm to create reliable benchmark datasets for translational initiation site (TIS) prediction. These datasets represent real-world transcripts, improving algorithm evaluation.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Translational initiation site (TIS) prediction is crucial in bioinformatics.
  • Reliable, representative, and accessible benchmark datasets are needed for algorithm comparison.
  • Existing datasets may not accurately reflect the general protein population.

Purpose of the Study:

  • To develop a general algorithm for constructing reliable mRNA sequence collections.
  • To create benchmark datasets representative of a given organism's protein population.
  • To evaluate the effectiveness of TIS prediction algorithms using the new datasets.

Main Methods:

  • Developed a general algorithm to construct sequence collections based on protein structural parameters.
  • Generated four representative transcript collections from model organisms.
  • Removed redundant homologous proteins to create a redundancy-free dataset.

Main Results:

  • The constructed datasets are reasonable representations of proteins from cellular proteomic studies.
  • Six state-of-the-art predictors were tested on the new datasets.
  • Comparative studies demonstrated the merits of the proposed datasets over existing ones.

Conclusions:

  • The algorithm is general, widely applicable, and creates representative "real world" datasets.
  • These datasets enable more accurate evaluation of TIS identification algorithms.
  • The approach can be extended for more selective datasets, aiding specific protein structure studies.