Yu Chuanhe, Gan Haiyun, Zhang Zhiguo
Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.
Institute for Cancer Genetics, Department of Pediatrics, and Department of Genetics and Development, Columbia University, Irving Cancer Research Center, New York, New York, USA.
Mol Cell Biol. 2017 Oct 13;37(21). doi: 10.1128/MCB.00190-17. Print 2017 Nov 1.
Three DNA polymerases, polymerases α, δ, and ε (Pol α, Pol δ, and Pol ε), are responsible for eukaryotic genome duplication. When DNA replication stress is encountered, DNA synthesis stalls until the stress is ameliorated. However, it is not known whether there is a difference in the association of each polymerase with active and stalled replication forks. Here, we show that each DNA polymerase has a distinct pattern of association with active and stalled replication forks. Pol α is enriched at extending Okazaki fragments of active and stalled forks. In contrast, although Pol δ contacts the nascent lagging strands of active and stalled forks, it binds to only the matured (and not elongating) Okazaki fragments of stalled forks. Pol ε has greater contact with the nascent single-stranded DNA (ssDNA) of the leading strand on active forks than on stalled forks. We propose that the configuration of DNA polymerases at stalled forks facilitates the resumption of DNA synthesis after stress removal.
三种DNA聚合酶,即聚合酶α、δ和ε(Pol α、Pol δ和Pol ε),负责真核生物基因组的复制。当遇到DNA复制压力时,DNA合成会暂停,直到压力得到缓解。然而,目前尚不清楚每种聚合酶与活跃和停滞的复制叉的结合是否存在差异。在这里,我们表明每种DNA聚合酶与活跃和停滞的复制叉具有不同的结合模式。Pol α在活跃和停滞叉的延伸冈崎片段上富集。相比之下,尽管Pol δ与活跃和停滞叉的新生滞后链接触,但它只与停滞叉的成熟(而非延伸)冈崎片段结合。与停滞叉相比,Pol ε在活跃叉上与前导链的新生单链DNA(ssDNA)有更多接触。我们提出,停滞叉处的DNA聚合酶配置有助于在压力消除后恢复DNA合成。