Abstract

Proteins belonging to the Tel2/Rad-5/Clk-2 family are conserved among eukaryotes and are involved in various cellular processes, such as cell proliferation, telomere maintenance, the biological clock, and the DNA damage checkpoint. However, the molecular mechanisms underlying the functions of these molecules remain largely unclear. Here we report that in the fission yeast, Schizosaccharomyces pombe, Tel2 is required for efficient phosphorylation of Mrc1, a mediator of DNA replication checkpoint signaling, and for activation of Cds1, a replication checkpoint kinase, when DNA replication is blocked by hydroxyurea. In fact, Tel2 is required for survival of replication fork arrest and for the replication checkpoint in cells lacking Chk1, another checkpoint kinase the role of which overlaps that of Cds1 in cell cycle arrest by replication block. In addition, Tel2 plays important roles in entry into S phase and in genome stability. Tel2 is essential for vegetative cell growth, and the tel2Delta strain accumulated cells with 1C DNA content after germination. In the absence of hydroxyurea, Tel2 is vital in the mutant lacking Swi1, a component of the replication fork protection complex, and multiple Rad22 DNA repair foci were frequently observed in Tel2-repressed swi1Delta cells especially at S phase. In contrast, the cds1Deltaswi1Delta mutant did not show such lethality. These results indicate that S. pombe Tel2 plays important roles in the Mrc1-mediated replication checkpoint as well as in the Cds1-independent regulation of genome integrity.

Highlights

  • Arrest until the DNA is fully repaired or until replication can resume [1,2,3,4,5]

  • Schizosaccharomyces pombe, among the two phosphatidylinositol 3-kinase-related proteins Rad3 and Tel1, Rad3 plays a major role in both the DNA damage checkpoint and the DNA replication checkpoint

  • Crb2 protein mediates the phosphorylation of Chk1 by Rad3-Rad26 kinase in response to DNA damage, whereas phosphorylation of Cds1 in response to replication fork stalling is mediated by Mrc1 [11,12,13,14]

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Summary

Yeast strains used in this study

Genotype hϪ leu ura4-D18 hϩ leu hϩ/hϪ tel2ϩ/tel2::ura4ϩ ade6-M216/ade6-M210 leu1-32/leu ura4-D18/ura4-D18 hϩ/hϪ tel2ϩ/tel2::ura4ϩ ade6-M216/ade6-M210 leu1-32/leu ura4-D18/ura4-D18 hϪ tel2-3HA:ura4ϩ cdc ade6-M216 ura4-D18 hϩ tel2-12myc:Kanr leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr leu ura4-D18 hϩ nmt81-tel2-12myc:LEU2ϩ:Kanr leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr cds1::ura4ϩ leu ura4-D18 hϪ rad22-YFP:Kanr swi1::LEU2ϩ leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr chk1::ura4ϩ leu ura4-D18 hϪ tel2-12myc:Kanr cds1::ura4ϩ ura4-D18 hϪ tel2-12myc:Kanr chk1::ura4ϩ ura4-D18 hϪ nmt81-tel2:12myc:LEU2ϩ:Kanr leu hϩ/hϪ ade6-M216/ade6-M210 leu1-32/leu ura4-D18/ura4-D18 hϪ tel2-12myc:Kanr mrc1-3HA:ura4ϩ leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr mrc1-3HA:ura4ϩ leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr chk1-3HA leu ura4-D18 hϪ tel2-12myc:Kanr chk1::ura4ϩ cds1::ura4ϩ ura4-D18 hϪ tel2-12myc:Kanr chk1-3HA leu ura4-D18 hϪ tel2-12myc:Kanr hϪ tel2-12myc:Kanr rad3::ura4ϩ ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr rad22-YFP:ura4ϩ leu ura4-D18 hϪ tel2-12myc:Kanr rad22-YFP:ura4ϩ ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr swi1::LEU2ϩ leu ura4-D18 hϪ tel2-12myc:Kanr swi1::LEU2ϩ leu ura4-D18 hϪ tel2-12myc:Kanr mrc1-3HA:ura4ϩ cds1::ura4ϩ leu ura4-D18 hϪ tel2-12myc:Kanr swi1::LEU2ϩ cds1::ura4ϩ leu ura4-D18 hϪ nmt81-tel2-12myc:LEU2ϩ:Kanr swi1::LEU2ϩ rad22-YFP:ura leu ura4-D18 telomeric DNA in vitro, suggesting that it regulates telomere length by binding to the ends of telomeres [35,36,37]. Ahmed et al [41] showed that rad-5 is allelic to clk-2, and cloning of the rad-5/ clk-2 gene revealed that it encodes a protein homologous to S. cerevisiae Tel2 [42, 43]. The rad-5/clk-2 mutant is sensitive to HU treatment and is defective in the DNA replication checkpoint [41]. Rad-5/Clk-2 has been shown to function downstream of ATL-1 (C. elegans ATR) in the DNA replication checkpoint pathway [44]. The molecular mechanisms of action of Rad-5/Clk-2 or hCLK2 in DNA replication remain unknown. We report the identification and characterization of tel2ϩ, the gene encoding the fission yeast TEL2/Rad-5/Clk-2related protein. We found that Tel is required for HU-induced activation of the Mrc1-Cds DNA replication checkpoint. The genetic interaction between tel and swi indicates that Tel plays an important role in maintenance of genome integrity, especially at S phase

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