Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Improving Translational Accuracy02:07

Improving Translational Accuracy

13.9K
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...
13.9K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

11.5K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
11.5K
Mismatch Repair01:20

Mismatch Repair

6.1K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
6.1K
Mismatch Repair01:36

Mismatch Repair

43.3K
Overview
43.3K
RNA Editing02:23

RNA Editing

9.6K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.6K
Proofreading01:31

Proofreading

8.4K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
8.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Enhanced IGFL1 translation in response to IL-1β is controlled by distinct 3'UTR elements.

PloS one·2026
Same author

Autoencoder/RandomForest-TabPFN for cross-cancer metabolomics: prostate and breast cancer diagnosis using paper spray and ion mobility-mass spectrometry techniques.

GigaScience·2026
Same author

A leader-repeat hairpin blocks extraneous CRISPR RNA production in diverse CRISPR-Cas13 systems.

The EMBO journal·2026
Same author

Comprehensive analysis of CRISPR array repeat mutations reveals subtype-specific patterns and links to spacer dynamics.

microLife·2026
Same author

The complexity of multiple CRISPR arrays in strains with (co-occurring) CRISPR systems.

microLife·2026
Same author

CoMPaseD: advanced planning of proteomic experiments aiming to identify small proteins.

microLife·2026

Related Experiment Video

Updated: Dec 20, 2025

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

5.0K

CopomuS-Ranking Compensatory Mutations to Guide RNA-RNA Interaction Verification Experiments.

Martin Raden1, Fabio Gutmann1, Michael Uhl1

  • 1Bioinformatics, Department of Computer Science, University Freiburg, Georges-Koehler-Allee 106, 79110 Freiburg, Germany.

International Journal of Molecular Sciences
|June 3, 2020
PubMed
Summary

Selecting compensatory mutations for RNA-RNA interaction verification is challenging. Our tool, CopomuS (COmPensatOry MUtation Selector), objectively ranks mutation candidates, improving experimental design for RNA interactions.

Keywords:
RNA-RNA interactioncompensatory mutationdesignmutationsRNA

More Related Videos

A Novel Saturation Mutagenesis Approach: Single Step Characterization of Regulatory Protein Binding Sites in RNA Using Phosphorothioates
11:49

A Novel Saturation Mutagenesis Approach: Single Step Characterization of Regulatory Protein Binding Sites in RNA Using Phosphorothioates

Published on: August 21, 2018

6.9K
A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
08:53

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency

Published on: September 15, 2021

3.1K

Related Experiment Videos

Last Updated: Dec 20, 2025

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

5.0K
A Novel Saturation Mutagenesis Approach: Single Step Characterization of Regulatory Protein Binding Sites in RNA Using Phosphorothioates
11:49

A Novel Saturation Mutagenesis Approach: Single Step Characterization of Regulatory Protein Binding Sites in RNA Using Phosphorothioates

Published on: August 21, 2018

6.9K
A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
08:53

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency

Published on: September 15, 2021

3.1K

Area of Science:

  • Computational Biology
  • Molecular Biology
  • Bioinformatics

Background:

  • In silico RNA-RNA interaction prediction identifies potential partners.
  • Experimental verification often uses compensatory mutations, but selection is subjective.
  • Objective criteria are needed to guide compensatory mutation selection.

Purpose of the Study:

  • Introduce CopomuS, a tool to objectively select compensatory mutations for RNA-RNA interactions.
  • Improve the reliability and efficiency of designing verification experiments.
  • Provide a computational aid for RNA-RNA interaction studies.

Main Methods:

  • Utilized the IntaRNA prediction tool for RNA-RNA interaction assessment.
  • Analyzed characteristics of experimentally validated RNA-RNA interactions from literature.
  • Developed CopomuS based on objective criteria derived from interaction analysis.
  • Evaluated CopomuS performance using validated compensatory mutations of prokaryotic sRNAs and target mRNAs.

Main Results:

  • CopomuS provides objective criteria for evaluating mutation effects on RNA-RNA interactions.
  • The tool outputs a reliable ranking of compensatory mutation candidates.
  • CopomuS predictions show high agreement with experimentally validated results.
  • The tool is integrated into the IntaRNA package and available as a webserver.

Conclusions:

  • CopomuS is a valuable tool for supporting the design of RNA-RNA interaction verification experiments.
  • Objective selection of compensatory mutations enhances experimental reliability.
  • The tool facilitates in silico analysis and in vitro validation of RNA interactions.