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Structures of active Hantaan virus polymerase uncover the mechanisms of Hantaviridae genome replication

Author

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  • Quentin Durieux Trouilleton

    (Univ. Grenoble Alpes, CNRS, CEA, IBS)

  • Sergio Barata-García

    (Aix-Marseille Université, CNRS, AFMB UMR)

  • Benoît Arragain

    (Univ. Grenoble Alpes, CNRS, CEA, IBS
    European Molecular Biology Laboratory (EMBL))

  • Juan Reguera

    (Aix-Marseille Université, CNRS, AFMB UMR
    INSERM, AFMB UMR)

  • Hélène Malet

    (Univ. Grenoble Alpes, CNRS, CEA, IBS
    Institut Universitaire de France (IUF))

Abstract

Hantaviruses are causing life-threatening zoonotic infections in humans. Their tripartite negative-stranded RNA genome is replicated by the multi-functional viral RNA-dependent RNA-polymerase. Here we describe the structure of the Hantaan virus polymerase core and establish conditions for in vitro replication activity. The apo structure adopts an inactive conformation that involves substantial folding rearrangement of polymerase motifs. Binding of the 5′ viral RNA promoter triggers Hantaan virus polymerase reorganization and activation. It induces the recruitment of the 3′ viral RNA towards the polymerase active site for prime-and-realign initiation. The elongation structure reveals the formation of a template/product duplex in the active site cavity concomitant with polymerase core widening and the opening of a 3′ viral RNA secondary binding site. Altogether, these elements reveal the molecular specificities of Hantaviridae polymerase structure and uncover the mechanisms underlying replication. They provide a solid framework for future development of antivirals against this group of emerging pathogens.

Suggested Citation

  • Quentin Durieux Trouilleton & Sergio Barata-García & Benoît Arragain & Juan Reguera & Hélène Malet, 2023. "Structures of active Hantaan virus polymerase uncover the mechanisms of Hantaviridae genome replication," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38555-w
    DOI: 10.1038/s41467-023-38555-w
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    1. Kathryn Tunyasuvunakool & Jonas Adler & Zachary Wu & Tim Green & Michal Zielinski & Augustin Žídek & Alex Bridgland & Andrew Cowie & Clemens Meyer & Agata Laydon & Sameer Velankar & Gerard J. Kleywegt, 2021. "Highly accurate protein structure prediction for the human proteome," Nature, Nature, vol. 596(7873), pages 590-596, August.
    2. Benoît Arragain & Grégory Effantin & Piotr Gerlach & Juan Reguera & Guy Schoehn & Stephen Cusack & Hélène Malet, 2020. "Pre-initiation and elongation structures of full-length La Crosse virus polymerase reveal functionally important conformational changes," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
    3. John Jumper & Richard Evans & Alexander Pritzel & Tim Green & Michael Figurnov & Olaf Ronneberger & Kathryn Tunyasuvunakool & Russ Bates & Augustin Žídek & Anna Potapenko & Alex Bridgland & Clemens Me, 2021. "Highly accurate protein structure prediction with AlphaFold," Nature, Nature, vol. 596(7873), pages 583-589, August.
    4. Ruchao Peng & Xin Xu & Jiamei Jing & Min Wang & Qi Peng & Sheng Liu & Ying Wu & Xichen Bao & Peiyi Wang & Jianxun Qi & George F. Gao & Yi Shi, 2020. "Structural insight into arenavirus replication machinery," Nature, Nature, vol. 579(7800), pages 615-619, March.
    5. Tomas Kouba & Dominik Vogel & Sigurdur R. Thorkelsson & Emmanuelle R. J. Quemin & Harry M. Williams & Morlin Milewski & Carola Busch & Stephan Günther & Kay Grünewald & Maria Rosenthal & Stephen Cusac, 2021. "Conformational changes in Lassa virus L protein associated with promoter binding and RNA synthesis activity," Nature Communications, Nature, vol. 12(1), pages 1-18, December.
    6. Benoît Arragain & Quentin Durieux Trouilleton & Florence Baudin & Jan Provaznik & Nayara Azevedo & Stephen Cusack & Guy Schoehn & Hélène Malet, 2022. "Structural snapshots of La Crosse virus polymerase reveal the mechanisms underlying Peribunyaviridae replication and transcription," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
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    1. Quentin Durieux Trouilleton & Dominique Housset & Paco Tarillon & Benoît Arragain & Hélène Malet, 2024. "Structural characterization of the oligomerization of full-length Hantaan virus polymerase into symmetric dimers and hexamers," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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