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Model-based analysis of DNA replication profiles: predicting replication fork velocity and initiation rate by profiling free-cycling cells

机译:DNA复制配置文件的基于模型的分析:通过分析自由循环细胞来预测复制叉的速度和起始速率

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摘要

Eukaryotic cells initiate DNA synthesis by sequential firing of hundreds of origins. This ordered replication is described by replication profiles, which measure the DNA content within a cell population. Here, we show that replication dynamics can be deduced from replication profiles of free-cycling cells. While such profiles lack explicit temporal information, they are sensitive to fork velocity and initiation capacity through the passive replication pattern, namely the replication of origins by forks emanating elsewhere. We apply our model-based approach to a compendium of profiles that include most viable budding yeast mutants implicated in replication. Predicted changes in fork velocity or initiation capacity are verified by profiling synchronously replicating cells. Notably, most mutants implicated in late (or early) origin effects are explained by global modulation of fork velocity or initiation capacity. Our approach provides a rigorous framework for analyzing DNA replication profiles of free-cycling cells.
机译:真核细胞通过顺序激发数百个来源来启动DNA合成。这种有序的复制由复制概况描述,该概况测量细胞群体内的DNA含量。在这里,我们表明复制动力学可以从自由循环细胞的复制概况中推导出来。尽管此类配置文件缺少明确的时间信息,但它们通过被动复制模式对分叉速度和启动能力敏感,即通过散发于其他位置的分叉来复制起点。我们将基于模型的方法应用于概要文件,该概要文件包括复制中涉及的大多数可行的出芽酵母突变体。通过分析同步复制的细胞,可以验证叉速或启动能力的预测变化。值得注意的是,大多数涉及晚期(或早期)起源效应的突变体是通过对叉子速度或启动能力的整体调节来解释的。我们的方法为分析自由循环细胞的DNA复制概况提供了严格的框架。

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