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p56 chk1 protein kinase is required for the DNA replication checkpoint at 37°C in fission yeast
Author(s) -
Francesconi Stefania,
Gre Muriel,
Bouvier Dominique,
Baldacci Giuseppe
Publication year - 1997
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/16.6.1332
Subject(s) - chek1 , g2 m dna damage checkpoint , biology , cyclin dependent kinase 1 , schizosaccharomyces pombe , cell cycle checkpoint , dna replication , dna damage , control of chromosome duplication , schizosaccharomyces , s phase , dna re replication , microbiology and biotechnology , checkpoint kinase 2 , mitotic catastrophe , replication factor c , eukaryotic dna replication , cell cycle , genetics , dna , saccharomyces cerevisiae , yeast , cell
Fission yeast p56 chk1 kinase is known to be involved in the DNA damage checkpoint but not to be required for cell cycle arrest following exposure to the DNA replication inhibitor hydroxyurea (HU). For this reason, p56 chk1 is considered not to be necessary for the DNA replication checkpoint which acts through the inhibitory phosphorylation of p34 cdc2 kinase activity. In a search for Schizosaccharomyces pombe mutants that abolish the S phase cell cycle arrest of a thermosensitive DNA polymerase δ strain at 37°C, we isolated two chk1 alleles. These alleles are proficient for the DNA damage checkpoint, but induce mitotic catastrophe in several S phase thermosensitive mutants. We show that the mitotic catastrophe correlates with a decreased level of tyrosine phosphorylation of p34 cdc2 . In addition, we found that the deletion of chk1 and the chk1 alleles abolish the cell cycle arrest and induce mitotic catastrophe in cells exposed to HU, if the cells are grown at 37°C. These findings suggest that chk1 is important for the maintenance of the DNA replication checkpoint in S phase thermosensitive mutants and that the p56 chk1 kinase must possess a novel function that prevents premature activation of p34 cdc2 kinase under conditions of impaired DNA replication at 37°C.