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Genetic Networks Required to Coordinate Chromosome Replication by DNA Polymerases α δ and ε in Saccharomyces cerevisiae

机译:酿酒酵母中通过DNA聚合酶αδ和ε协调染色体复制所需的遗传网络

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摘要

Three major DNA polymerases replicate the linear eukaryotic chromosomes. DNA polymerase α-primase (Pol α) and DNA polymerase δ (Pol δ) replicate the lagging-strand and Pol α and DNA polymerase ε (Pol ε) the leading-strand. To identify factors affecting coordination of DNA replication, we have performed genome-wide quantitative fitness analyses of budding yeast cells containing defective polymerases. We combined temperature-sensitive mutations affecting the three replicative polymerases, Pol α, Pol δ, and Pol ε with genome-wide collections of null and reduced function mutations. We identify large numbers of genetic interactions that inform about the roles that specific genes play to help Pol α, Pol δ, and Pol ε function. Surprisingly, the overlap between the genetic networks affecting the three DNA polymerases does not represent the majority of the genetic interactions identified. Instead our data support a model for division of labor between the different DNA polymerases during DNA replication. For example, our genetic interaction data are consistent with biochemical data showing that Pol ε is more important to the Pre-Loading complex than either Pol α or Pol δ. We also observed distinct patterns of genetic interactions between leading- and lagging-strand DNA polymerases, with particular genes being important for coupling proliferating cell nuclear antigen loading/unloading (, ) with nucleosome assembly (chromatin assembly factor 1, histone regulatory HIR complex). Overall our data reveal specialized genetic networks that affect different aspects of leading- and lagging-strand DNA replication. To help others to engage with these data we have generated two novel, interactive visualization tools, DIXY and Profilyzer.
机译:三种主要的DNA聚合酶可复制线性真核染色体。 DNA聚合酶α-引发酶(Polα)和DNA聚合酶δ(Polδ)复制了滞后链,而Polα和DNA聚合酶ε(Polε)形成了前导链。为了确定影响DNA复制协调的因素,我们对含有缺陷的聚合酶的酵母细胞进行了全基因组定量适应性分析。我们将影响三种复制性聚合酶Polα,Polδ和Polε的温度敏感突变与无效和降低功能突变的全基因组集合相结合。我们鉴定出大量的遗传相互作用,这些相互作用说明特定基因在帮助Polα,Polδ和Polε功能中所起的作用。出人意料的是,影响这三种DNA聚合酶的遗传网络之间的重叠并不代表所鉴定的大多数遗传相互作用。相反,我们的数据支持在DNA复制过程中不同DNA聚合酶之间的分工模型。例如,我们的遗传相互作用数据与生化数据一致,表明Polε对预加载复合物比Polα或Polδ更重要。我们还观察到了前导链和滞后链DNA聚合酶之间遗传相互作用的不同模式,其中特定的基因对于将增殖的细胞核抗原加载/卸载与核小体组装(染色质组装因子1,组蛋白调节性HIR复合体)耦合很重要。总体而言,我们的数据揭示了影响领先和落后DNA复制的不同方面的专门遗传网络。为了帮助其他人处理这些数据,我们生成了两个新颖的交互式可视化工具DIXY和Profilyzer。

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