Wenshuo Zhang, Jiawei Xu, Jiayi Yang, Guojun Shi, Jiale Wu, Ning Gao, Jianxun Feng, Qing Li
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引用次数: 0
Abstract
Deficiencies in replication-coupled (RC) nucleosome assembly often lead to reduced DNA replication rate, but the precise mechanism underlying this process remains unsolved. Here, we discovered that H3-H4, but not H2A-H2B, mediates the interaction between FACT and the primase-polymerase complex DNA Pol α. This interaction stimulates the DNA polymerase activity of Pol α, and is indispensable for Okazaki fragment synthesis and replication fork progression. Moreover, the Pol1-N domain of Pol α provides a specific binding site for FACT and H3-H4. Furthermore, CAF-1 and Rtt106-mediated replication-coupled nucleosome assembly pathways regulate this interaction. Together, we propose that the FACT-(H3-H4)-Pol α interaction acts as a “Pre-Warning System” that regulates DNA replication, ensuring proper coordination between DNA synthesis and nucleosome assembly.
复制耦合(RC)核小体组装缺陷通常会导致DNA复制率降低,但这一过程的确切机制仍未解决。我们在这里发现,H3-H4(而非 H2A-H2B)介导了 FACT 与底物酶-聚合酶复合体 DNA Pol α 之间的相互作用,这种相互作用刺激了 Pol α 的 DNA 聚合酶活性,对于冈崎片段的合成和复制叉的进展是不可或缺的。此外,Pol α的Pol1-N结构域为FACT和H3-H4提供了一个特异性结合位点。此外,CAF-1 和 Rtt106 介导的复制耦合核小体组装途径也会调节这种相互作用。综上所述,我们认为 FACT-(H3-H4)-Pol α 相互作用是调节 DNA 复制的 "预警系统",可确保 DNA 合成与核小体组装之间的适当协调。