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Cryo-EM uncovers a sequential mechanism for RNA polymerase I pausing and stalling at abasic DNA lesions

Author

Listed:
  • Alicia Santos-Aledo

    (CSIC)

  • Adrián Plaza-Pegueroles

    (CSIC)

  • Marta Sanz-Murillo

    (CSIC)

  • Federico M. Ruiz

    (CSIC)

  • Peini Hou

    (UCSD)

  • Jun Xu

    (UCSD)

  • David Gil-Carton

    (Basque Resource for Electron Microscopy
    University of the Basque Country
    Basque Foundation for Science)

  • Dong Wang

    (UCSD)

  • Carlos Fernández-Tornero

    (CSIC)

Abstract

During synthesis of the ribosomal RNA precursor, RNA polymerase I (Pol I) monitors DNA integrity but its response to DNA damage remains poorly studied. Abasic sites are among the most prevalent DNA lesions in eukaryotic cells, and their detection is critical for cell survival. We report cryo-EM structures of Pol I in different stages of stalling at abasic sites, supported by in vitro transcription studies. Slow nucleotide addition opposite abasic sites occurs through base sandwiching between the RNA 3′-end and the Pol I bridge helix. Templating abasic sites can also cause Pol I cleft opening, which enables the A12 subunit to access the active center. Nucleotide addition opposite the lesion induces a translocation intermediate where DNA bases tilt to form hydrogen bonds with the new RNA base. These findings reveal unique mechanisms of Pol I stalling at abasic sites, differing from arrest by bulky lesions or abasic site handling by RNA polymerase II.

Suggested Citation

  • Alicia Santos-Aledo & Adrián Plaza-Pegueroles & Marta Sanz-Murillo & Federico M. Ruiz & Peini Hou & Jun Xu & David Gil-Carton & Dong Wang & Carlos Fernández-Tornero, 2025. "Cryo-EM uncovers a sequential mechanism for RNA polymerase I pausing and stalling at abasic DNA lesions," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60536-4
    DOI: 10.1038/s41467-025-60536-4
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    References listed on IDEAS

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    1. Seychelle M. Vos & Lucas Farnung & Henning Urlaub & Patrick Cramer, 2018. "Structure of paused transcription complex Pol II–DSIF–NELF," Nature, Nature, vol. 560(7720), pages 601-606, August.
    2. Michael Pilsl & Corinne Crucifix & Gabor Papai & Ferdinand Krupp & Robert Steinbauer & Joachim Griesenbeck & Philipp Milkereit & Herbert Tschochner & Patrick Schultz, 2016. "Structure of the initiation-competent RNA polymerase I and its implication for transcription," Nature Communications, Nature, vol. 7(1), pages 1-12, November.
    3. Jun Xu & Indrajit Lahiri & Wei Wang & Adam Wier & Michael A. Cianfrocco & Jenny Chong & Alissa A. Hare & Peter B. Dervan & Frank DiMaio & Andres E. Leschziner & Dong Wang, 2017. "Structural basis for the initiation of eukaryotic transcription-coupled DNA repair," Nature, Nature, vol. 551(7682), pages 653-657, November.
    4. Matthew J. Rossi & Prashant K. Kuntala & William K. M. Lai & Naomi Yamada & Nitika Badjatia & Chitvan Mittal & Guray Kuzu & Kylie Bocklund & Nina P. Farrell & Thomas R. Blanda & Joshua D. Mairose & An, 2021. "A high-resolution protein architecture of the budding yeast genome," Nature, Nature, vol. 592(7853), pages 309-314, April.
    5. Yashar Sadian & Florence Baudin & Lucas Tafur & Brice Murciano & Rene Wetzel & Felix Weis & Christoph W. Müller, 2019. "Molecular insight into RNA polymerase I promoter recognition and promoter melting," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    6. Christoph Engel & Sarah Sainsbury & Alan C. Cheung & Dirk Kostrewa & Patrick Cramer, 2013. "RNA polymerase I structure and transcription regulation," Nature, Nature, vol. 502(7473), pages 650-655, October.
    7. Simon Neyer & Michael Kunz & Christian Geiss & Merle Hantsche & Victor-Valentin Hodirnau & Anja Seybert & Christoph Engel & Margot P. Scheffer & Patrick Cramer & Achilleas S. Frangakis, 2016. "Structure of RNA polymerase I transcribing ribosomal DNA genes," Nature, Nature, vol. 540(7634), pages 607-610, December.
    8. Alan C. M. Cheung & Patrick Cramer, 2011. "Structural basis of RNA polymerase II backtracking, arrest and reactivation," Nature, Nature, vol. 471(7337), pages 249-253, March.
    9. Phong Quoc Nguyen & Sonia Huecas & Amna Asif-Laidin & Adrián Plaza-Pegueroles & Beatrice Capuzzi & Noé Palmic & Christine Conesa & Joël Acker & Juan Reguera & Pascale Lesage & Carlos Fernández-Tornero, 2023. "Structural basis of Ty1 integrase tethering to RNA polymerase III for targeted retrotransposon integration," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
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