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

Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
DNA Topoisomerases02:02

DNA Topoisomerases

Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types.  Type I...
The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
Nucleic Acid Structure01:25

Nucleic Acid Structure

The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA has a double-helix structure. The...
Replication in Prokaryotes01:32

Replication in Prokaryotes

DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...

You might also read

Related Articles

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

Sort by
Same author

In Silico implementation of evolutionary paradigm in therapy design: Towards anti-cancer therapy as Darwinian process.

Journal of theoretical biology·2019
Same author

A new conceptual framework for the therapy by optimized multidimensional pulses of therapeutic activity. The case of multiple myeloma model.

Journal of theoretical biology·2018
Same author

The effect of cortisol on gamma-glutamyl transpeptidase activity in the glycogen body and lumbosacral segments of developing chick spinal cord.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience·2014
Same author

Kerr constant of vesicle-like droplets.

Journal of biological physics·2013
Same author

Optimization aspects of carcinogenesis.

Medical hypotheses·2009
Same author

Subcellular redistribution of trimeric G-proteins--potential mechanism of desensitization of hormone response: internalization, solubilization, down-regulation.

Physiological research·2008

Related Experiment Video

Updated: Jul 12, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

Monomer dynamics in single- and double-stranded DNA coils.

J Tothova1, B Brutovsky, V Lisy

  • 1Institute of Physics, P.J. Safarik University, Jesenna 5, 041 54 Kosice, Slovakia.

The European Physical Journal. E, Soft Matter
|September 4, 2007
PubMed
Summary

This study refines polymer physics models for DNA dynamics. New data confirm that double- and single-stranded DNA predominantly follow Zimm-type kinetics, not Rouse kinetics, improving theoretical agreement.

More Related Videos

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase
07:37

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase

Published on: September 27, 2024

Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
15:57

Visualizing Single-molecule DNA Replication with Fluorescence Microscopy

Published on: October 9, 2009

Related Experiment Videos

Last Updated: Jul 12, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase
07:37

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase

Published on: September 27, 2024

Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
15:57

Visualizing Single-molecule DNA Replication with Fluorescence Microscopy

Published on: October 9, 2009

Area of Science:

  • Polymer Physics
  • Biophysics
  • Statistical Mechanics

Background:

  • Previous work interpreted polymer monomer kinetics using bead-spring theory and the Rouse-Zimm model.
  • Experimental data on DNA dynamics were recently corrected, necessitating a re-evaluation of theoretical fits.

Purpose of the Study:

  • To fit the Rouse-Zimm model to newly corrected experimental data for DNA dynamics.
  • To re-evaluate the kinetic behavior of double- and single-stranded DNA based on updated measurements.

Main Methods:

  • Utilized fluorescence correlation spectroscopy data.
  • Optimized the joint Rouse-Zimm polymer model to experimental measurements.
  • Analyzed monomer dynamics, including draining effects and scaling laws.

Main Results:

  • The updated data show significantly better agreement with the Rouse-Zimm theory than previous data.
  • Confirmed that double-stranded DNA (dsDNA) primarily exhibits Zimm-type kinetics.
  • Single-stranded DNA (ssDNA) also predominantly behaves as a Zimm polymer.

Conclusions:

  • The main conclusions from the prior study are upheld, though some polymer parameters have been refined.
  • The findings support the dominance of Zimm-type kinetics for both dsDNA and ssDNA, challenging prior proposals.
  • Analysis of draining effects and scaling laws (t^1/2 for Rouse, t^2/3 for Zimm) further supports the Zimm model's applicability.