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Mismatch Repair01:20

Mismatch Repair

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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.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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Homologous Recombination02:31

Homologous Recombination

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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

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Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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Base Excision Repair01:54

Base Excision Repair

22.7K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
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Proofreading01:31

Proofreading

6.4K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity 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...
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Related Experiment Video

Updated: Jul 28, 2025

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
08:48

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

Published on: October 13, 2011

13.1K

Pulling short DNA with mismatch base pairs.

Navin Singh1, Nehal Mathur2

  • 1Department of Physics, Birla Institute of Technology and Science, Pilani, Rajasthan, 333 031, India. navin@pilani.bits-pilani.ac.in.

European Biophysics Journal : EBJ
|May 30, 2023
PubMed
Summary
This summary is machine-generated.

DNA defects compromise gene expression accuracy. This study reveals DNA with defects denatures at lower temperatures and exhibits distinct behaviors in thermal versus force ensembles.

Keywords:
DNA denaturationDefectPBD model

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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
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Related Experiment Videos

Last Updated: Jul 28, 2025

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
08:48

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

Published on: October 13, 2011

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Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis

Published on: June 19, 2018

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Area of Science:

  • Molecular Biology
  • Biophysics
  • Genetics

Background:

  • Gene replication errors can lead to DNA molecule defects.
  • These DNA defects can compromise gene expression accuracy.

Purpose of the Study:

  • To investigate the stability of DNA with varying numbers of defects (2-16).
  • To compare DNA denaturation processes in thermal and force ensembles.

Main Methods:

  • Utilized a statistical model to calculate DNA melting points.
  • Analyzed DNA stability across different defect concentrations.

Main Results:

  • DNA with defects denatures at a lower temperature compared to intact DNA.
  • Denaturation patterns differ significantly between thermal and force ensembles.
  • The pulling point is a critical factor in DNA denaturation within the force ensemble.

Conclusions:

  • DNA defects alter denaturation characteristics.
  • The ensemble type (thermal vs. force) influences DNA defect manifestation.