Mohebi Saed, Lambert Sarah A E, Carr Antony M
Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, John Maynard Smith Building, Falmer, Brighton, BN1 9RQ, UK.
Methods Mol Biol. 2015;1300:239-59. doi: 10.1007/978-1-4939-2596-4_15.
The study of how eukaryotic cells overcome problems associated with dysfunctional DNA replication forks is assisted by experimental systems that allow site-specific replication fork arrest. Here we provide protocols for the use of the fission yeast RTS1 replication fork barrier. The RTS1 barrier is a directional, or polar, replication fork barrier that evolved to ensure directional replication of the fission yeast mating-type locus. We have moved the 859 bp RTS1 sequence to another locus in the genome and demonstrated that it arrests replication forks in a dysfunctional confirmation and that replication is restarted within ~20 min by the action of homologous recombination. We describe here the barrier constructs currently available, the methods by which we regulate the activity of the barrier, how to synchronize cells for analysis of replication intermediates by 2D gel electrophoresis, and the use of a replication slippage assay to measure fork fidelity.
对真核细胞如何克服与功能失调的DNA复制叉相关问题的研究,可借助能实现位点特异性复制叉停滞的实验系统来推进。在此,我们提供使用裂殖酵母RTS1复制叉屏障的方案。RTS1屏障是一种定向的,即极性的复制叉屏障,其进化目的是确保裂殖酵母交配型位点的定向复制。我们已将859 bp的RTS1序列转移至基因组中的另一位点,并证明它能在功能失调的状态下使复制叉停滞,且通过同源重组作用,复制在约20分钟内重新启动。我们在此描述目前可用的屏障构建体、调节屏障活性的方法、如何同步细胞以便通过二维凝胶电泳分析复制中间体,以及使用复制滑移测定法来测量叉保真度。