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Structural insights into how Cas9 targets nucleosomes

Author

Listed:
  • Reina Nagamura

    (The University of Tokyo)

  • Tomoya Kujirai

    (The University of Tokyo)

  • Junko Kato

    (The University of Tokyo)

  • Yutaro Shuto

    (The University of Tokyo)

  • Tsukasa Kusakizako

    (The University of Tokyo)

  • Hisato Hirano

    (The University of Tokyo)

  • Masaki Endo

    (National Agriculture and Food Research Organization)

  • Seiichi Toki

    (National Agriculture and Food Research Organization
    Yokohama City University
    Ryukoku University)

  • Hiroaki Saika

    (National Agriculture and Food Research Organization)

  • Hitoshi Kurumizaka

    (The University of Tokyo)

  • Osamu Nureki

    (The University of Tokyo)

Abstract

The CRISPR-associated endonuclease Cas9 derived from prokaryotes is used as a genome editing, which targets specific genomic loci by single guide RNAs (sgRNAs). The eukaryotes, the target of genome editing, store their genome DNA in chromatin, in which the nucleosome is a basic unit. Despite previous structural analyses focusing on Cas9 cleaving free DNA, structural insights into Cas9 targeting of DNA within nucleosomes are limited, leading to uncertainties in understanding how Cas9 operates in the eukaryotic genome. In the present study, we perform native-polyacrylamide gel electrophoresis (PAGE) analyses and find that Cas9 targets the linker DNA and the entry-exit DNA region of the nucleosome but not the DNA tightly wrapped around the histone octamer. We further determine cryo-electron microscopy (cryo-EM) structure of the Cas9-sgRNA-nucleosome ternary complex that targets linker DNA in nucleosomes. The structure suggests interactions between Cas9 and nucleosomes at multiple sites. Mutants that reduce the interaction between nucleosomal DNA and Cas9 improve nucleosomal DNA cleavage activity in vitro, although inhibition by the interaction between Cas9 and nucleosomes is limited in vivo. These findings will contribute to the development of novel genome editing tools in chromatin.

Suggested Citation

  • Reina Nagamura & Tomoya Kujirai & Junko Kato & Yutaro Shuto & Tsukasa Kusakizako & Hisato Hirano & Masaki Endo & Seiichi Toki & Hiroaki Saika & Hitoshi Kurumizaka & Osamu Nureki, 2024. "Structural insights into how Cas9 targets nucleosomes," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54768-z
    DOI: 10.1038/s41467-024-54768-z
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    References listed on IDEAS

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    1. Carolin Anders & Ole Niewoehner & Alessia Duerst & Martin Jinek, 2014. "Structural basis of PAM-dependent target DNA recognition by the Cas9 endonuclease," Nature, Nature, vol. 513(7519), pages 569-573, September.
    2. Karolin Luger & Armin W. Mäder & Robin K. Richmond & David F. Sargent & Timothy J. Richmond, 1997. "Crystal structure of the nucleosome core particle at 2.8 Å resolution," Nature, Nature, vol. 389(6648), pages 251-260, September.
    3. Martin Pacesa & Luuk Loeff & Irma Querques & Lena M. Muckenfuss & Marta Sawicka & Martin Jinek, 2022. "R-loop formation and conformational activation mechanisms of Cas9," Nature, Nature, vol. 609(7925), pages 191-196, September.
    4. Mikihiro Shibata & Hiroshi Nishimasu & Noriyuki Kodera & Seiichi Hirano & Toshio Ando & Takayuki Uchihashi & Osamu Nureki, 2017. "Real-space and real-time dynamics of CRISPR-Cas9 visualized by high-speed atomic force microscopy," Nature Communications, Nature, vol. 8(1), pages 1-9, December.
    5. Fuqiang Chen & Xiao Ding & Yongmei Feng & Timothy Seebeck & Yanfang Jiang & Gregory D. Davis, 2017. "Targeted activation of diverse CRISPR-Cas systems for mammalian genome editing via proximal CRISPR targeting," Nature Communications, Nature, vol. 8(1), pages 1-12, April.
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