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. 2020 Dec 2;48(21):12169-12187. doi: 10.1093/nar/gkaa963.
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.
高度保守的 Tof1/Timeless 蛋白可最大程度减少复制应激,并促进正常的 DNA 复制。它们介导着 DNA 复制检查点(DRC),即蛋白质分叉阻挡物处叉的稳定暂停,在复制应激(RS)期间解旋酶和聚合酶功能的偶联,以及在叉前优先解决 DNA 拓扑学压力。在这里,我们证明了酿酒酵母 Timeless 蛋白 Tof1 在 DRC 信号转导和 DNA 拓扑学压力缓解中的作用需要该蛋白的独特的 N 端和 C 端区域,而 Tof1 的其他功能则与其与组成型结合伙伴 Csm3/Tipin 的稳定相互作用密切相关。通过将 Tof1 在 DRC 中的作用与叉稳定和偶联分开,我们表明 Tof1 在检查点激活和复制体稳定性方面具有不同的活性,以确保在复制应激后 DNA 复制的有效完成。