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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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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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Overview of DNA Repair02:25

Overview of DNA Repair

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In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
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DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

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In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
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Base Excision Repair01:54

Base Excision Repair

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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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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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Related Experiment Video

Updated: Jul 6, 2025

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage
10:44

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage

Published on: January 31, 2018

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Compartmentalizing damaged DNA: A double-edged sword.

Emily Georgiades1, Nicola Crosetto2, Magda Bienko2

  • 1Human Technopole, Viale Rita Levi-Montalcini 1, 20157 Milano, Italy.

Molecular Cell
|January 5, 2024
PubMed
Summary
This summary is machine-generated.

Researchers discovered a new "damaged" chromatin compartment that aids DNA repair but may also raise cancer risk by promoting translocations.

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Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
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Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
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Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging

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Last Updated: Jul 6, 2025

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Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
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Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging

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Area of Science:

  • Genetics
  • Molecular Biology
  • Cell Biology

Background:

  • DNA double-strand breaks (DSBs) are severe DNA lesions.
  • DSBs can lead to genomic instability and cancer if not repaired accurately.
  • Chromatin organization plays a critical role in DNA repair processes.

Purpose of the Study:

  • To identify and characterize novel structural components involved in DNA double-strand break repair.
  • To investigate the functional implications of these components in both DNA repair and genome stability.

Main Methods:

  • High-resolution microscopy techniques to visualize chromatin structures.
  • Biochemical assays to assess DNA repair factor recruitment.
  • Genetic manipulation to study the role of the D compartment in DSB repair and translocation formation.

Main Results:

  • A novel chromatin compartment, the "damaged" or "D" compartment, was identified.
  • The D compartment is enriched in DNA repair factors and facilitates DSB repair.
  • Formation of the D compartment is associated with an increased risk of oncogenic translocations.

Conclusions:

  • The D compartment represents a newly discovered functional unit of chromatin organization during DNA repair.
  • While crucial for efficient DSB repair, the D compartment's activity carries a risk of potentially oncogenic translocations.
  • Understanding the D compartment could lead to new therapeutic strategies targeting cancer-related genomic instability.