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Torsion is a dynamic regulator of DNA replication stalling and reactivation

Author

Listed:
  • Xiaomeng Jia

    (Cornell University, Howard Hughes Medical Institute
    Cornell University, Department of Physics & LASSP)

  • Xiang Gao

    (Cornell University, Howard Hughes Medical Institute
    Cornell University, Department of Physics & LASSP)

  • Shuming Zhang

    (Cornell University, Howard Hughes Medical Institute
    Cornell University, Department of Physics & LASSP)

  • James T. Inman

    (Cornell University, Howard Hughes Medical Institute
    Cornell University, Department of Physics & LASSP)

  • Yifeng Hong

    (Cornell University, Department of Electrical and Computer Engineering)

  • Anupam Singh

    (Rutgers University, Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School)

  • Fahad Rashid

    (Johns Hopkins University School of Medicine, Department of Biophysics and Biophysical Chemistry)

  • James M. Berger

    (Johns Hopkins University School of Medicine, Department of Biophysics and Biophysical Chemistry)

  • Smita S. Patel

    (Rutgers University, Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School)

  • Michelle D. Wang

    (Cornell University, Howard Hughes Medical Institute
    Cornell University, Department of Physics & LASSP)

Abstract

DNA’s helical structure necessitates replisome rotation relative to DNA during replication, creating inevitable topological challenges. How replication generates and overcomes torsional stress remains unclear. Here, we developed a high-resolution, label-free, real-time assay to track DNA rotation by T7 replisome and its slowing under torsional stress. While helicase or DNA polymerase (DNAP) alone is a weak rotary motor, together they form the most powerful DNA rotary motor yet studied, generating ~22 pN·nm torque before stalling, twice that of E. coli RNA polymerase. Upon stalling, helicase-DNAP interactions stabilize the fork; without them, regression can extend hundreds of base pairs. Prolonged stalling inactivates the replisome, but excess DNAP, aided by interactions with helicase, promotes restart. Gyrase supports steady replication and enables timely restart of stalled forks. These findings demonstrate that helicase-DNAP synergy is essential for maintaining fork integrity under torsion, and that torsion is a key regulator of replication stalling and reactivation.

Suggested Citation

  • Xiaomeng Jia & Xiang Gao & Shuming Zhang & James T. Inman & Yifeng Hong & Anupam Singh & Fahad Rashid & James M. Berger & Smita S. Patel & Michelle D. Wang, 2025. "Torsion is a dynamic regulator of DNA replication stalling and reactivation," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
    • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-65567-5
    DOI: 10.1038/s41467-025-65567-5
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