Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Homologous Recombination02:31

Homologous Recombination

50.6K
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...
50.6K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.8K
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,...
5.8K
Nucleotide Excision Repair01:08

Nucleotide Excision Repair

37.2K
Overview
37.2K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.7K
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...
12.7K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.0K
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...
6.0K
Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

7.0K
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:
7.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The multifaceted roles of the Ctf4 replisome hub in the maintenance of genome integrity.

DNA repair·2024
Same author

SnapShot: DNA repair pathways.

Molecular cell·2024
Same author

SnapShot: Tolerating replication stress.

Molecular cell·2024
Same author

FANCJ DNA helicase is recruited to the replisome by AND-1 to ensure genome stability.

EMBO reports·2024
Same author

PCNA recruits cohesin loader Scc2 to ensure sister chromatid cohesion.

Nature structural & molecular biology·2023
Same author

Rad51-mediated replication of damaged templates relies on monoSUMOylated DDK kinase.

Nature communications·2022

Related Experiment Video

Updated: Jul 17, 2025

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
06:24

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

Published on: February 13, 2019

8.1K

Hot on RAD51C: structure and functions of RAD51C-XRCC3.

Barnabas Szakal1, Dana Branzei1,2

  • 1IFOM ETS, The AIRC Institute of Molecular Oncology, Milan, Italy.

Molecular Oncology
|September 8, 2023
PubMed
Summary

Researchers solved the structure of the RAD51C-XRCC3 (CX3) heterodimer, revealing two distinct roles in DNA replication fork stability and restart mechanisms during replication stress.

Keywords:
DNA bindingFork protectionFork restartRAD51 filament cappingRAD51 paralogsRAD51-XRCC3

More Related Videos

Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy
11:40

Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy

Published on: June 25, 2013

12.1K
Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
07:55

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

Published on: September 11, 2022

1.9K

Related Experiment Videos

Last Updated: Jul 17, 2025

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
06:24

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

Published on: February 13, 2019

8.1K
Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy
11:40

Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy

Published on: June 25, 2013

12.1K
Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
07:55

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

Published on: September 11, 2022

1.9K

Area of Science:

  • Molecular Biology
  • DNA Replication
  • Protein Structure

Background:

  • RAD51C-XRCC3 (CX3) is a crucial heterodimer involved in DNA repair and replication fork stability.
  • Understanding the structural basis of CX3 function is essential for comprehending genome integrity maintenance.

Purpose of the Study:

  • To determine the high-resolution structure of the RAD51C-XRCC3 (CX3) heterodimer bound to an ATP analog.
  • To elucidate the distinct functional roles of the CX3 heterodimer in maintaining replication fork stability.

Main Methods:

  • X-ray crystallography to solve the structure of the CX3 heterodimer.
  • Biochemical assays to assess the functional roles of identified structural interfaces.

Main Results:

  • The study identified two primary structural interfaces within the CX3 heterodimer.
  • One interface facilitates CX3 assembly on nascent DNA, crucial for replication fork restart after stress.
  • The second interface is vital for 5' RAD51 filament capping, influencing filament dynamics and fork protection.

Conclusions:

  • The solved CX3 structure reveals separable roles in replication fork stability and restart.
  • CX3's ability to assemble on DNA and cap filaments are distinct functions critical for genome stability.