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Delineating the position of rad4+/cut5+ within the DNA-structure checkpoint pathways in Schizosaccharomyces pombe.
Harris, Sheila; Kemplen, Caroline; Caspari, Thomas; Chan, Christopher; Lindsay, Howard D; Poitelea, Marius; Carr, Antony M; Price, Clive.
Afiliación
  • Harris S; Krebs Institute for Biomolecular Research, Department of Molecular Biology and Biotechnology, University of Sheffield, PO Box 594, Western Bank, Sheffield S10 2TN, UK.
J Cell Sci ; 116(Pt 17): 3519-29, 2003 Sep 01.
Article en En | MEDLINE | ID: mdl-12865439
The fission yeast BRCT domain protein Rad4/Cut5 is required for genome integrity checkpoint responses and DNA replication. Here we address the position at which Rad4/Cut5 acts within the checkpoint response pathways. Rad4 is shown to act upstream of the effector kinases Chk1 and Cds1, as both Chk1 phosphorylation and Cds1 kinase activity require functional Rad4. Phosphorylation of Rad9, Rad26 and Hus1 in response to either DNA damage or inhibition of DNA replication are independent of Rad4/Cut5 checkpoint function. Further we show that a novel, epitope-tagged allele of rad4+/cut5+ acts as a dominant suppressor of the checkpoint deficiencies of rad3-, rad26- and rad17- mutants. Suppression results in the restoration of mitotic arrest and is dependent upon the remaining checkpoint Rad proteins and the two effector kinases. High-level expression of the rad4+/cut5+ allele in rad17 mutant cells restores the nuclear localization of Rad9, but this does not fully account for the observed suppression. We conclude from these data that Rad4/Cut5 acts with Rad3, Rad26 and Rad17 to effect the checkpoint response, and a model for its function is discussed.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Quinasas / Schizosaccharomyces / Transglutaminasas / Proteínas de Ciclo Celular / Proteínas de Schizosaccharomyces pombe / Proteínas de Unión al ADN Idioma: En Revista: J Cell Sci Año: 2003 Tipo del documento: Article Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Quinasas / Schizosaccharomyces / Transglutaminasas / Proteínas de Ciclo Celular / Proteínas de Schizosaccharomyces pombe / Proteínas de Unión al ADN Idioma: En Revista: J Cell Sci Año: 2003 Tipo del documento: Article Pais de publicación: Reino Unido