RNA-Triggered Protein Cleavage and Applications by the CRISPR Cas7-11-Csx29 Complex

The type III-E CRISPR–Cas7-11 effector binds a CRISPR RNA (crRNA) and the putative protease Csx29 and catalyzes crRNA-guided RNA cleavage. We report cryo–electron microscopy structures of the Cas7-11–crRNA–Csx29 complex with and without target RNA (tgRNA), and demonstrate that tgRNA binding induces conformational changes in Csx29. Biochemical experiments revealed tgRNA-dependent cleavage of the accessory protein Csx30 by Csx29. Reconstitution of the system in bacteria showed that Csx30 cleavage yields toxic protein fragments that cause growth arrest, which is regulated by Csx31. Csx30 binds Csx31 and the associated sigma factor RpoE (RNA polymerase, extracytoplasmic E), suggesting that Csx30-mediated RpoE inhibition modulates the cellular response to infection. We engineered the Cas7-11–Csx29–Csx30 system for programmable RNA sensing in mammalian cells. Overall, the Cas7-11–Csx29 effector is an RNA-dependent nuclease-protease.

Researchers

Omar Abudayyeh / Jonathan Gootenberg / Kaiyi Jiang / Hiroshi Nishimasu / Kazuki Kato / Cian Schmitt-Ulms

Departments: McGovern Institute for Brain Research, Biological Engineering, Brain and Cognitive Sciences
Technology Areas: Biotechnology: DNA & RNA Editing
Impact Areas: Healthy Living

  • rna-triggered protein cleavage and applications by the crispr cas7-11-csx29 complex
    United States of America | Pending
  • rna-triggered protein cleavage and applications by the crispr cas7-11-csx29 complex
    Patent Cooperation Treaty | Published application

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