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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...
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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...
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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...
Gene Conversion02:08

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Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair01:36

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Related Experiment Video

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Analyzing and Building Nucleic Acid Structures with 3DNA
16:24

Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

DNA bending and sugar switching.

S Kamath1, M H Sarma, V B Zhurkin

  • 1a Institute of Biomolecular Stereodynamics, Department of Chemistry, University at Albany , SUNY 1400 Washington Avenue , Albany , NY , 12222.

Journal of Biomolecular Structure & Dynamics
|May 22, 2012
PubMed
Summary
This summary is machine-generated.

DNA sugar conformation shifts between B-like and A-like forms at A-tracts, influencing DNA bending. This dynamic process may guide protein binding to DNA junctions.

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Area of Science:

  • Molecular Biology
  • Biophysics
  • Structural Biology

Background:

  • DNA structure is crucial for its biological functions.
  • A-tracts in DNA are known to influence DNA conformation and protein binding.
  • Understanding sugar pucker dynamics is key to deciphering DNA flexibility.

Purpose of the Study:

  • To investigate sugar conformation equilibria in DNA duplexes with AAA tracts.
  • To elucidate the role of sugar conformation in DNA bending and helical parameters.
  • To propose a mechanism for protein recognition at DNA junctions.

Main Methods:

  • High-frequency antiphase Nuclear Magnetic Resonance (NMR) spectroscopy.
  • Computer simulations of antiphase NMR spectra.
  • Calculation of DNA helical parameters.

Main Results:

  • A 50-60% probability of sugar switching from S-conformer (B-like) to N-conformer (A-like) at the 3'-end of the A-tract was observed.
  • This sugar switch creates a purine-pyrimidine step with heteronomous characteristics.
  • The local B-A junction compresses the interphosphate distance and affects DNA bending parameters.

Conclusions:

  • DNA sugar conformation dynamics, particularly the mix of S and N conformers, contribute to DNA bending.
  • The heteronomous deformation in A(n)C motifs may serve as an initial recognition site for DNA-binding proteins.
  • DNA bending in A(n)C stretches is a complex dynamic process involving local conformational variations.