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Rpd3L Contributes to the DNA Damage Sensitivity ofSaccharomyces cerevisiaeCheckpoint Mutants
Author(s) -
Belén GómezGonzález,
Harshil Patel,
Anne Early,
John F.X. Diffley
Publication year - 2018
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.118.301817
Subject(s) - g2 m dna damage checkpoint , biology , dna damage , chek1 , saccharomyces cerevisiae , checkpoint kinase 2 , genetics , histone , microbiology and biotechnology , dna repair , cell cycle checkpoint , mutation , histone deacetylase , gene , dna , cell cycle
DNA replication forks that are stalled by DNA damage activate an S-phase checkpoint that prevents irreversible fork arrest and cell death. The increased cell death caused by DNA damage in budding yeast cells lacking the Rad53 checkpoint protein kinase is partially suppressed by deletion of the EXO1 gene. Using a whole-genome sequencing approach, we identified two additional genes, RXT2 and RPH1 , whose mutation can also partially suppress this DNA damage sensitivity. We provide evidence that RXT2 and RPH1 act in a common pathway, which is distinct from the EXO1 pathway. Analysis of additional mutants indicates that suppression works through the loss of the Rpd3L histone deacetylase complex. Our results suggest that the loss or absence of histone acetylation, perhaps at stalled forks, may contribute to cell death in the absence of a functional checkpoint.

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