Larsen Nicolai B, Hickson Ian D, Mankouri Hocine W
The Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.
Methods Mol Biol. 2018;1672:295-309. doi: 10.1007/978-1-4939-7306-4_20.
Site-specific arrest of DNA replication is a useful tool for analyzing cellular responses to DNA replication perturbation. The E. coli Tus-Ter replication barrier can be reconstituted in eukaryotic cells as a system to engineer an unscheduled collision between a replication fork and an "alien" impediment to DNA replication. To further develop this system as a versatile tool, we describe a set of reagents and a detailed protocol that can be used to engineer Tus-Ter barriers into any locus in the budding yeast genome. Because the Tus-Ter complex is a bipartite system with intrinsic DNA replication-blocking activity, the reagents and protocols developed and validated in yeast could also be optimized to engineer site-specific replication fork barriers into other eukaryotic cell types.
DNA复制的位点特异性停滞是分析细胞对DNA复制扰动反应的有用工具。大肠杆菌Tus-Ter复制屏障可以在真核细胞中重建,作为一种在复制叉与DNA复制的“外来”障碍之间制造意外碰撞的系统。为了将该系统进一步开发成一种通用工具,我们描述了一组试剂和详细方案,可用于在芽殖酵母基因组的任何位点构建Tus-Ter屏障。由于Tus-Ter复合物是一个具有内在DNA复制阻断活性的二分系统,在酵母中开发和验证的试剂和方案也可以进行优化,以便在其他真核细胞类型中构建位点特异性复制叉屏障。