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Related Concept Videos

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...
DNA as a Genetic Template02:05

DNA as a Genetic Template

Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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 Helicases00:55

DNA Helicases

DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
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...
Replication in Eukaryotes01:29

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...

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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

Bubbles in DNA melting.

Rodrigo Gonzalez1, Yan Zeng, Vassili Ivanov

  • 1Department of Physics and Astronomy, University of California Los Angeles, Los Angeles, CA 90095-1547, USA.

Journal of Physics. Condensed Matter : an Institute of Physics Journal
|August 6, 2011
PubMed
Summary
This summary is machine-generated.

Studying intermediate-sized DNA and RNA oligomers reveals insights into base pairing and stacking. Analysis of bubble length offers a more nuanced understanding of melting transitions than base dissociation alone.

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Area of Science:

  • Biophysics
  • Molecular Biology
  • Computational Chemistry

Background:

  • The DNA melting transition is crucial for understanding nucleic acid stability and function.
  • Existing models often simplify the complex interplay of base pairing and stacking interactions.

Purpose of the Study:

  • To investigate the DNA melting transition using intermediate-sized oligomers.
  • To evaluate models of nucleic acid thermodynamics, focusing on base pairing and stacking.
  • To explore the significance of bubble length in DNA/RNA melting dynamics.

Main Methods:

  • Review of prior experimental work on DNA melting transitions.
  • New measurements of elastic energy in sharp bends of single-stranded DNA and RNA.
  • Analysis of cooperativity parameters and modification of the nearest-neighbor model.
  • Experimental studies on the stability of DNA and RNA hairpins with short loops.

Main Results:

  • Intermediate oligomers provide critical tests for thermodynamic models.
  • Bubble length dynamics offer more detailed insights than fraction of dissociated bases.
  • The transition is rarely a simple two-state process, with nucleation sizes near 1 base pair.
  • A modified nearest-neighbor model accounting for separate pairing and stacking fits experimental data.

Conclusions:

  • Intermediate oligomers are key to refining nucleic acid stability models.
  • Further experimental and theoretical work is needed to reconcile model predictions with experimental observations.
  • Understanding hairpin stability in short loops is essential for nucleic acid structure-function relationships.