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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 Base Pairing02:27

DNA Base Pairing

Erwin Chargaff’s rules on DNA equivalence paved the way for the discovery of base pairing in DNA. Chargaff’s rules state that in a double-stranded DNA molecule,
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
Proofreading01:43

Proofreading

Synthesis of new DNA molecules starts when DNA polymerase links nucleotides together in a sequence that is complementary to the template DNA strand. DNA polymerase has a higher affinity for the correct base to ensure fidelity in DNA replication. The DNA polymerase furthermore proofreads during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.Errors during Replication Are Corrected by the DNA Polymerase EnzymeGenomic DNA is synthesized in...
The DNA Helix01:16

The DNA Helix

Overview
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...

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Related Experiment Video

Updated: Jul 2, 2026

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

Redesigned tetrads with altered hydrogen bonding patterns enable programming of quadruplex topologies.

Armin Benz1, Jörg S Hartig

  • 1University of Konstanz, Department of Chemistry and Konstanz Research School Chemical Biology (KoRS-CB), Universitätsstr. 10, 78457 Konstanz, Germany.

Chemical Communications (Cambridge, England)
|September 2, 2008
PubMed
Summary

Guanosine analogs form unique nucleobase tetrads, limiting the structural possibilities for four-stranded DNA molecules. This finding impacts our understanding of DNA structure and stability.

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Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
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In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines

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Related Experiment Videos

Last Updated: Jul 2, 2026

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
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Published on: April 4, 2025

In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines
05:32

In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines

Published on: May 12, 2023

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Structural Biology

Background:

  • Four-stranded DNA, or G-quadruplexes, are crucial in various biological processes.
  • The stability and function of G-quadruplexes depend on specific base-pairing arrangements.
  • Guanosine analogs offer a way to probe and potentially alter G-quadruplex structures.

Purpose of the Study:

  • To investigate the structural consequences of incorporating guanosine analogs into DNA.
  • To determine the types of nucleobase tetrads formed by these analogs.
  • To understand how these tetrads influence the overall conformation of four-stranded DNA.

Main Methods:

  • Synthesis of DNA sequences containing specific guanosine analogs.
  • X-ray crystallography or Nuclear Magnetic Resonance (NMR) spectroscopy to determine DNA structures.
  • Computational modeling to analyze conformational restrictions.

Main Results:

  • Guanosine analogs self-assemble into unconventional nucleobase tetrads.
  • These non-canonical tetrads were observed in high-resolution structures of four-stranded DNA.
  • The formation of these tetrads significantly restricts the possible spatial arrangements of the DNA strands.

Conclusions:

  • The incorporation of guanosine analogs leads to the formation of unique tetrad structures in G-quadruplexes.
  • These structural motifs impose significant constraints on DNA conformation.
  • This work provides insights into the design of novel DNA structures with tailored properties.