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 Experiment Videos

Hypothesis: hypersensitive plasmid copy number control for ColE1

M Ehrenberg1

  • 1Department of Molecular Biology, Uppsala University, Sweden. ehrenberg@xray.bmc.uu.se

Biophysical Journal
|January 1, 1996
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population.

Molecular vision·2010
Same author

Image correlation microscopy for uniform illumination.

Journal of microscopy·2010
Same author

Maximum rrn promoter activity in Escherichia coli at saturating concentrations of free RNA polymerase.

Biochimie·2009
Same author

Varying rate of RNA chain elongation during rrn transcription in Escherichia coli.

Journal of bacteriology·2009
Same author

Spontaneous separation of bi-stable biochemical systems into spatial domains of opposite phases.

Systems biology·2006
Same author

Rate, accuracy and cost of ribosomes in bacterial cells.

Biochimie·2006
Same journal

Tau protein differentially affects Piezo1 and Kir2.1 channels in brain capillary endothelial cells.

Biophysical journal·2026
Same journal

Emergent Intercellular Junction Stability during Cyclic Tissue Loading.

Biophysical journal·2026
Same journal

Enhanced-Sampling Simulations Reveal Distinct Intermediates in SARS-CoV-2 FSE Pseudoknot Interconversion.

Biophysical journal·2026
Same journal

Structure-based simulations of the full Flock House virus capsid reveal pathways and energetics of an infection-critical peptide externalization event.

Biophysical journal·2026
Same journal

Quantifying the Peripheral Surface Information Entropy from Conformational Ensembles of Globular Protein-Peptide Complexes.

Biophysical journal·2026
Same journal

Anisotropic unbinding and location-dependent hovering of a kinesin motor head over microtubule.

Biophysical journal·2026
See all related articles

This study reveals how plasmid ColE1 replication is regulated by RNA I and the Rom protein. This mechanism ensures stable plasmid copy numbers and precise duplication timing within the cell cycle.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Plasmid ColE1 replication initiation is controlled by cis-acting RNA II.
  • Antisense RNA I regulates RNA II activity, with concentration proportional to plasmid copy number.
  • The Rom protein enhances RNA I inhibition of RNA II.

Purpose of the Study:

  • To investigate the regulatory mechanism of ColE1 plasmid replication initiation.
  • To understand how RNA I and Rom protein influence plasmid stability and duplication timing.
  • To analyze the impact of transcription rates on plasmid loss and cell cycle synchronization.

Main Methods:

  • Mathematical modeling of RNA I inhibition kinetics.
  • Analysis of plasmid replication probability based on RNA I concentration.

Related Experiment Videos

  • Simulation of plasmid loss rates and duplication time distributions.
  • Main Results:

    • The RNA I concentration-dependent inhibition mechanism reduces plasmid loss.
    • Increased transcription rates of RNA II lead to decreased plasmid loss and narrower duplication time distributions.
    • The Rom protein further enhances plasmid stability and narrows duplication time distributions for single-copy plasmids.

    Conclusions:

    • The described regulatory mechanism ensures stable plasmid copy numbers and timely replication.
    • Fine-tuning transcription rates and Rom protein activity optimizes plasmid maintenance.
    • This system provides a model for understanding genetic element stability and cell cycle regulation.