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Analysis of Rad3 and Chk1 protein kinases defines different checkpoint responses.

Research output: Contribution to journalJournal articlepeer-review

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  • Rui G. Martinho
  • Howard D. Lindsay
  • Gail Flaggs
  • Anthony J DeMaggio
  • Merl F. Hoekstra
  • Antony M. Carr
  • Nicola J. Bentley
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<mark>Journal publication date</mark>15/12/1998
<mark>Journal</mark>EMBO Journal
Issue number24
Volume17
Number of pages11
Pages (from-to)7239-7249
Publication StatusPublished
<mark>Original language</mark>English

Abstract

Eukaryotic cells respond to DNA damage and S phase replication blocks by arresting cell-cycle progression through the DNA structure checkpoint pathways. In Schizosaccharomyces pombe, the Chk1 kinase is essential for mitotic arrest and is phosphorylated after DNA damage. During S phase, the Cds1 kinase is activated in response to DNA damage and DNA replication blocks. The response of both Chk1 and Cds1 requires the six 'checkpoint Rad' proteins (Rad1, Rad3, Rad9, Rad17, Rad26 and Hus1). We demonstrate that DNA damage-dependent phosphorylation of Chk1 is also cell-cycle specific, occurring primarily in late S phase and G2, but not during M/G1 or early S phase. We have also isolated and characterized a temperature-sensitive allele of rad3. Rad3 functions differently depending on which checkpoint pathway is activated. Following DNA damage, rad3 is required to initiate but not maintain the Chk1 response. When DNA replication is inhibited, rad3 is required for both initiation and maintenance of the Cds1 response. We have identified a strong genetic interaction between rad3 and cds1, and biochemical evidence shows a physical interaction is possible between Rad3 and Cds1, and between Rad3 and Chk1 in vitro. Together, our results highlight the cell-cycle specificity of the DNA structure-dependent checkpoint response and identify distinct roles for Rad3 in the different checkpoint responses.