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Updated: Jun 9, 2025

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Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
Published on: September 11, 2022
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Cohesin complex oligomerization maintains end-tethering at DNA double-strand breaks.
Jamie Phipps1,2, Mathias Toulouze1,2, Cécile Ducrot1,2
1UMR Stabilité Génétique Cellules Souches et Radiations, Université Paris Cité, INSERM, CEA, Fontenay-aux-Roses, France.
Nature Cell Biology
|November 1, 2024
Summary
Cohesin
Area of Science:
- Molecular Biology
- Genetics
- Cell Biology
Background:
- Genome stability relies on efficient DNA double-strand break (DSB) repair.
- Timely DSB repair requires keeping broken DNA ends tethered.
- Two DSB end-tethering pathways exist in Saccharomyces cerevisiae: the MRX complex and an Exo1-dependent pathway with unknown bridging proteins.
Purpose of the Study:
- To identify the bridging proteins involved in the Exo1-dependent DSB end-tethering pathway.
- To elucidate the role of cohesin oligomerization in DSB repair.
Main Methods:
- Utilized Saccharomyces cerevisiae as a model organism.
- Employed microscopy-based microfluidic experiments.
- Investigated the function of cohesin, its loader, and Smc5/6 in conjunction with Exo1.
Main Results:
- Cohesin, its loader, and Smc5/6 were identified as key players in tethering DSB ends with Exo1.
- Cohesin impaired in oligomerization failed to tether DSB ends, highlighting the importance of this function.
- Cohesin was shown to play a direct role in DSB repair by ensuring end-tethering, beyond its role in sister chromatid cohesion.
Conclusions:
- Cohesin's oligomerization is essential for preventing DSB end-separation and promoting repair.
- This study reveals a novel mechanism for cohesin in safeguarding genome integrity through DSB end-tethering.
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