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Related Concept Videos

Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
Lagging Strand Synthesis01:59

Lagging Strand Synthesis

During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
The Replisome03:01

The Replisome

DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
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...
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...

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Related Experiment Video

Updated: May 22, 2026

Design and Synthesis of a Reconfigurable DNA Accordion Rack
07:44

Design and Synthesis of a Reconfigurable DNA Accordion Rack

Published on: August 15, 2018

Cooperativity, entropy, and effective concentration in DNA origami self-replication.

Heng Ni1, Feng Zhou1, Guolong Zhu2

  • 1Department of Physics, New York University, New York, NY 10003, USA.

Science Advances
|May 20, 2026
PubMed
Summary

This study presents a simplified thermodynamic model for complex DNA structures, predicting melting temperatures and aiding in the design of DNA nanotechnology devices.

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Area of Science:

  • Biotechnology
  • Nanotechnology
  • Molecular Biology

Background:

  • DNA nanotechnology has rapidly advanced, yielding novel structures and devices.
  • The thermodynamics governing complex DNA assemblies are not fully understood.

Purpose of the Study:

  • To develop a simplified thermodynamic model for predicting the assembly, melting, and activation of complex DNA structures.
  • To provide a framework for designing cooperative interactions in DNA-based systems.

Main Methods:

  • A two-state (open-close) model was employed, incorporating effective concentration and entropy effects.
  • The model was validated using DNA origami self-replication and Förster Resonance Energy Transfer (FRET) experiments.

Main Results:

  • The model accurately predicts melting temperatures, showing a significant shift due to cooperativity.
  • Experimental validation demonstrated the model's predictive power for DNA assemblies of increasing complexity.

Conclusions:

  • The simplified thermodynamic model offers a practical approach to understanding complex DNA assembly thermodynamics.
  • This model is valuable for designing dynamic DNA nanostructures and adaptable to other molecular systems.