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

Riboswitches01:56

Riboswitches

Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...

You might also read

Related Articles

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

Sort by
Same author

Computational selection of allosteric RNAs: A review.

International journal of biological macromolecules·2026
Same author

Rational Design of Chimeric Antisense Oligonucleotides that Target FMN Riboswitch mRNAs and Inhibit the Growth of Methicillin-Resistant <i>Staphylococcus aureus</i>.

ACS infectious diseases·2025
Same author

Targeting Bacterial Adenylate Kinase mRNA with a Chimeric Antisense Oligonucleotide for Rational Antibacterial Drug Development.

Molecules (Basel, Switzerland)·2025
Same author

Computational Design of Allosteric Ribozymes via Genetic Algorithms.

Methods in molecular biology (Clifton, N.J.)·2024
Same author

Antisense and Functional Nucleic Acids in Rational Drug Development.

Antibiotics (Basel, Switzerland)·2024
Same author

General and Specific Cytotoxicity of Chimeric Antisense Oligonucleotides in Bacterial Cells and Human Cell Lines.

Antibiotics (Basel, Switzerland)·2024

Related Experiment Video

Updated: May 16, 2026

Assay Development for High-Throughput Drug Screening Against Mycobacteria
07:50

Assay Development for High-Throughput Drug Screening Against Mycobacteria

Published on: October 25, 2024

Riboswitch-based antibacterial drug discovery using high-throughput screening methods.

Robert Penchovsky1, Cvetelina C Stoilova

  • 1Sofia University "St. Kliment Ohridski", Department of Genetics, Sofia, Bulgaria. robert.penchovsky@hotmail.com

Expert Opinion on Drug Discovery
|November 21, 2012
PubMed
Summary
This summary is machine-generated.

Bacterial riboswitches are RNA molecules that control gene expression. Researchers have identified 17 classes of these RNA switches in 36 bacterial pathogens, offering new targets for developing novel antibiotics.

More Related Videos

A High-throughput, High-content, Liquid-based C. elegans Pathosystem
09:44

A High-throughput, High-content, Liquid-based C. elegans Pathosystem

Published on: July 1, 2018

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses
11:34

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses

Published on: May 5, 2014

Related Experiment Videos

Last Updated: May 16, 2026

Assay Development for High-Throughput Drug Screening Against Mycobacteria
07:50

Assay Development for High-Throughput Drug Screening Against Mycobacteria

Published on: October 25, 2024

A High-throughput, High-content, Liquid-based C. elegans Pathosystem
09:44

A High-throughput, High-content, Liquid-based C. elegans Pathosystem

Published on: July 1, 2018

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses
11:34

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses

Published on: May 5, 2014

Area of Science:

  • Molecular Biology
  • Genetics
  • Microbiology

Background:

  • Bacterial riboswitches are RNA domains in mRNA that bind metabolites to regulate gene expression.
  • These RNA switches allow bacteria to sense physiological changes and control metabolic pathways.
  • The discovery of riboswitches has rapidly expanded over the last decade, revealing their widespread use in bacteria.

Purpose of the Study:

  • To review mechanisms of bacterial riboswitch gene expression control.
  • To highlight riboswitches in human bacterial pathogens as potential antibacterial drug targets.
  • To discuss high-throughput screening approaches for riboswitch-targeted drug development.

Main Methods:

  • Literature review of bacterial riboswitches and their functions.
  • Analysis of riboswitch classes found in human bacterial pathogens.
  • Discussion of in silico, in vitro, and in vivo screening methods for drug discovery.

Main Results:

  • 17 distinct classes of bacterial riboswitches identified in 36 human pathogens.
  • Riboswitches regulate the synthesis of essential metabolites in bacteria.
  • These riboswitches represent promising targets for novel antibacterial agents.

Conclusions:

  • Bacterial riboswitches are crucial regulatory elements with therapeutic potential.
  • Targeting riboswitches in pathogens offers a strategy to combat antibiotic resistance.
  • High-throughput screening is vital for developing new antibiotics against bacterial riboswitches.