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Separable functions of Tof1/Timeless in intra-S-checkpoint signalling, replisome stability and DNA topological stress.
Westhorpe, Rose; Keszthelyi, Andrea; Minchell, Nicola E; Jones, David; Baxter, Jonathan.
Affiliation
  • Westhorpe R; Genome Damage and Stability Centre, School of Life Sciences, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex BN1 9RQ, UK.
  • Keszthelyi A; Genome Damage and Stability Centre, School of Life Sciences, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex BN1 9RQ, UK.
  • Minchell NE; Genome Damage and Stability Centre, School of Life Sciences, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex BN1 9RQ, UK.
  • Jones D; Genome Damage and Stability Centre, School of Life Sciences, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex BN1 9RQ, UK.
  • Baxter J; Genome Damage and Stability Centre, School of Life Sciences, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex BN1 9RQ, UK.
Nucleic Acids Res ; 48(21): 12169-12187, 2020 12 02.
Article in En | MEDLINE | ID: mdl-33166393
The highly conserved Tof1/Timeless proteins minimise replication stress and promote normal DNA replication. They are required to mediate the DNA replication checkpoint (DRC), the stable pausing of forks at protein fork blocks, the coupling of DNA helicase and polymerase functions during replication stress (RS) and the preferential resolution of DNA topological stress ahead of the fork. Here we demonstrate that the roles of the Saccharomyces cerevisiae Timeless protein Tof1 in DRC signalling and resolution of DNA topological stress require distinct N and C terminal regions of the protein, whereas the other functions of Tof1 are closely linked to the stable interaction between Tof1 and its constitutive binding partner Csm3/Tipin. By separating the role of Tof1 in DRC from fork stabilisation and coupling, we show that Tof1 has distinct activities in checkpoint activation and replisome stability to ensure the viable completion of DNA replication following replication stress.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Saccharomyces cerevisiae / Gene Expression Regulation, Fungal / Cell Cycle Proteins / Saccharomyces cerevisiae Proteins / DNA-Binding Proteins Language: En Journal: Nucleic Acids Res Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Saccharomyces cerevisiae / Gene Expression Regulation, Fungal / Cell Cycle Proteins / Saccharomyces cerevisiae Proteins / DNA-Binding Proteins Language: En Journal: Nucleic Acids Res Year: 2020 Type: Article