Reference: da Silva SCR and Bastos de Oliveira FM (2025) The bur1-107 mutant delays G1/S transition and alleviates hydroxyurea sensitivity in checkpoint-deficient yeast. Genetics

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Abstract


In Saccharomyces cerevisiae, the cyclin-dependent kinase Bur1 is primarily known for its role in promoting transcription elongation, thereby regulating gene expression. In this study, we investigated the genetic interactions between a hypomorphic BUR1 allele (bur1-107) and null mutants of the checkpoint kinases Mec1 and Rad53. Remarkably, bur1-107 alleviated the sensitivity of mec1 and rad53 mutants to hydroxyurea (HU), suggesting that Bur1 activity becomes detrimental when checkpoint signaling is impaired. Furthermore, the bur1-107 mutation delayed the G1-to-S phase transition, implicating Bur1 as a key player in cell cycle progression. In HU-treated mec1 mutants, bur1-107 reduced γ-H2A accumulation, promoted S-phase resumption, and suppressed the formation of sub-G1 populations. Together, these findings suggest that Bur1-driven G1-to-S phase progression exacerbates DNA damage and cell death in checkpoint-deficient cells exposed to HU. This study highlights a novel role for Bur1 in modulating the cellular response to replication stress in checkpoint-compromised cells.

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Journal Article
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da Silva SCR, Bastos de Oliveira FM
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