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

Genetic Screens02:46

Genetic Screens

Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...
Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).Mechanisms of Genetic VariationThe original sources of genetic variation are mutations,...
Global Regulatory Systems01:28

Global Regulatory Systems

Global regulatory systems in bacteria enable rapid and coordinated responses to environmental changes by integrating sensory inputs with gene expression, ensuring efficient adaptation to fluctuating conditions. Key global regulatory mechanisms include regulons, two-component systems, sigma factors, and secondary messengers.Regulons and Global RegulatorsA regulon is a collection of genes and operons controlled by a common global regulator. These regulators enable bacteria to prioritize resource...

You might also read

Related Articles

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

Sort by
Same author

Structure and dynamics in the low-density phase of a two-dimensional cellular automaton model of traffic flow.

Physical review. E·2026
Same author

Differentiation between regulated and disrupted growth arrests allows tailoring of effective treatments for antibiotic persistence.

Science advances·2026
Same author

Uncovering phenotypic inheritance from single cells with Microcolony-seq.

Cell·2025
Same author

Effect of preferential node deletion on the structure of networks that evolve via preferential attachment.

Physical review. E·2025
Same author

Impact of Population Mask Wearing on Covid-19 Post Lockdown.

Infectious microbes & diseases·2025
Same author

Cancer drug-tolerant persister cells: from biological questions to clinical opportunities.

Nature reviews. Cancer·2024

Related Experiment Video

Updated: Jul 16, 2026

Sealable Femtoliter Chamber Arrays for Cell-free Biology
13:44

Sealable Femtoliter Chamber Arrays for Cell-free Biology

Published on: March 11, 2015

Stochastic simulations of genetic switch systems.

Adiel Loinger1, Azi Lipshtat, Nathalie Q Balaban

  • 1Racah Institute of Physics, The Hebrew University, Jerusalem 91904, Israel.

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|March 16, 2007
PubMed
Summary

Genetic switches with mutual repression can be bistable, showing two stable states. This study reveals bistability can occur even without cooperative binding, depending on network structure and stochastic effects.

More Related Videos

Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion
09:17

Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion

Published on: March 1, 2022

An Ecdysone Receptor-based Singular Gene Switch for Deliberate Expression of Transgene with Robustness, Reversibility, and Negligible Leakiness
06:21

An Ecdysone Receptor-based Singular Gene Switch for Deliberate Expression of Transgene with Robustness, Reversibility, and Negligible Leakiness

Published on: May 7, 2018

Related Experiment Videos

Last Updated: Jul 16, 2026

Sealable Femtoliter Chamber Arrays for Cell-free Biology
13:44

Sealable Femtoliter Chamber Arrays for Cell-free Biology

Published on: March 11, 2015

Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion
09:17

Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion

Published on: March 1, 2022

An Ecdysone Receptor-based Singular Gene Switch for Deliberate Expression of Transgene with Robustness, Reversibility, and Negligible Leakiness
06:21

An Ecdysone Receptor-based Singular Gene Switch for Deliberate Expression of Transgene with Robustness, Reversibility, and Negligible Leakiness

Published on: May 7, 2018

Area of Science:

  • Systems biology
  • Molecular genetics
  • Biophysics

Background:

  • Genetic switch systems with mutual repression are crucial for cellular decision-making.
  • These systems often exhibit bistability, allowing for stable gene expression states.
  • Cooperative binding has been considered essential for achieving bistability.

Purpose of the Study:

  • To investigate bistability in genetic switch systems with mutual repression.
  • To explore the role of network structure and stochastic effects on bistability.
  • To determine conditions for bistability in the absence of cooperative binding.

Main Methods:

  • Deterministic methods: rate equations.
  • Stochastic methods: master equation and Monte Carlo simulations.
  • Analysis of genetic switch variants with varying binding and degradation mechanisms.

Main Results:

  • Identified parameter ranges for bistability in genetic switches.
  • Demonstrated that bistability can emerge without cooperative binding through network structure and stochasticity.
  • Evaluated the average time between spontaneous transitions as a function of biological parameters.

Conclusions:

  • Bistability in genetic switches is achievable through a combination of network topology and inherent stochasticity.
  • Cooperative binding is not a mandatory requirement for genetic switch bistability.
  • Stochastic effects play a significant role in the dynamics and stability of genetic switches.