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
- transcription factor
- cell proliferation
- placebo controlled
- induced apoptosis
- genome wide
- clinical trial
- cell cycle arrest
- cell free
- oxidative stress
- cell death
- electronic health record
- locally advanced
- squamous cell carcinoma
- dna binding
- radiation therapy
- gene expression
- signaling pathway
- cell wall