Retzer Thomas M, Rajappa Lional T, Takahashi Masateru, Hamdan Samir M, Duderstadt Karl E
Structure and Dynamics of Molecular Machines, Max Planck Institute of Biochemistry; Martinsried, Germany.
Department of Bioscience, Technical University of Munich; Garching, Germany.
bioRxiv. 2025 Apr 7:2025.04.01.646591. doi: 10.1101/2025.04.01.646591.
During chromosome replication, unwinding by the helicase and synthesis by the polymerases can lead to overwinding and supercoiling of DNA. The mechanical consequences of these events and resulting local dynamics at the replication fork are not well understood. To address these issues, we developed a transverse DNA flow-stretching approach to spatially resolve the parental, leading and lagging strands in real-time. Using bacteriophage T7 as a model system, this approach revealed bursts of high-speed replisome rotation that support continuous DNA synthesis. Surprisingly, excessive rotation does not reduce replisome speed, but increases pausing, reduces processivity, and increases polymerase exchange. Taken together, our observations reveal intrinsic pathways to overcome challenges posed by unfavorable DNA topologies during DNA replication.
在染色体复制过程中,解旋酶的解旋作用和聚合酶的合成作用会导致DNA过度缠绕和超螺旋化。这些事件的力学后果以及复制叉处由此产生的局部动力学尚未得到充分理解。为了解决这些问题,我们开发了一种横向DNA流动拉伸方法,以实时在空间上解析亲代链、前导链和后随链。以噬菌体T7作为模型系统,这种方法揭示了支持连续DNA合成的高速复制体旋转爆发。令人惊讶的是,过度旋转并不会降低复制体速度,反而会增加停顿、降低持续合成能力并增加聚合酶交换。综合来看,我们的观察结果揭示了克服DNA复制过程中不利DNA拓扑结构带来的挑战的内在途径。