A CDK-Dependent Phosphorylation of a Novel Domain of Rif1 Regulates its Function during Telomere Damage and Other Types of Stress

Rif1 mediates telomere length, DNA replication, and DNA damage responses in budding yeast. Previous work identified several posttranslational modifications of Rif1, however none of these was shown to mediate the molecular or cellular responses to DNA damage, including telomere damage. We searched for such modifications using immunoblotting methods and the cdc13-1 and tlc1 Delta models of telomere damage. We found that Rif1 is phosphorylated during telomere damage, and that serines 57 and 110 within a novel phospho-gate domain (PGD) of Rif1 are important for this modification, in cdc13-1 cells. The phosphorylation of Rif1 appeared to inhibit its accumulation on damaged chromosomes and the proliferation of cells with telomere damage. Moreover, we found that checkpoint kinases were upstream of this Rif1 phosphorylation and that the Cdk1 activity was essential for maintaining it. Apart from telomere damage, S57 and S110 were essential for Rif1 phosphorylation during the treatment of cells with genotoxic agents or during mitotic stress. We propose a speculative Pliers model to explain the role of the PGD phosphorylation during telomere and other types of damage.

Automated summary

Rif1 is involved in telomere length regulation, DNA replication, and DNA damage responses in budding yeast. We identified a novel phosphorylation of Rif1 during telomere damage, and serines 57 and 110 within a phospho-gate domain (PGD) were found to be important for this modification. The phosphorylation of Rif1 inhibits its accumulation on damaged chromosomes and the proliferation of cells with telomere damage.