Concurrent D-loop cleavage by Mus81 and Yen1 yields half-crossover precursors.
Raquel CarreiraTomas Lama-DiazMaria CrugeirasF Javier AguadoMarek SebestaLumír KrejčíMiguel G BlancoPublished in: Nucleic acids research (2024)
Homologous recombination involves the formation of branched DNA molecules that may interfere with chromosome segregation. To resolve these persistent joint molecules, cells rely on the activation of structure-selective endonucleases (SSEs) during the late stages of the cell cycle. However, the premature activation of SSEs compromises genome integrity, due to untimely processing of replication and/or recombination intermediates. Here, we used a biochemical approach to show that the budding yeast SSEs Mus81 and Yen1 possess the ability to cleave the central recombination intermediate known as the displacement loop or D-loop. Moreover, we demonstrate that, consistently with previous genetic data, the simultaneous action of Mus81 and Yen1, followed by ligation, is sufficient to recreate the formation of a half-crossover precursor in vitro. Our results provide not only mechanistic explanation for the formation of a half-crossover, but also highlight the critical importance for precise regulation of these SSEs to prevent chromosomal rearrangements.
Keyphrases
- cell cycle
- dna repair
- dna damage
- open label
- copy number
- double blind
- cell proliferation
- transcription factor
- placebo controlled
- induced apoptosis
- genome wide
- cell cycle arrest
- cell death
- electronic health record
- clinical trial
- oxidative stress
- randomized controlled trial
- locally advanced
- radiation therapy
- machine learning
- rectal cancer
- cell wall
- artificial intelligence