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Structural basis of Cas8-independent Cas3 recruitment in Type I-F2 CRISPR–Cas /

Title: Structural basis of Cas8-independent Cas3 recruitment in Type I-F2 CRISPR–Cas /
Authors: Perry, Thomas Noé; Mais, Christopher-Nils; Sanchez-Londono, Mariana; Steinchen, Wieland; Plitzko, Pauline A; Randau, Lennart; Pausch, Patrick; Innis, C Axel; Bange, Gert
Source: Nucleic acids research., Oxford : Oxford University Press, 2026, vol. 54, iss. 5, art. no. gkag136, p. 1-18. ; ISSN 0305-1048 ; eISSN 1362-4962
Publication Year: 2026
Collection: Vilnius University Virtual Library (VU VL) / Vilniaus universitetas virtuali biblioteka
Description: CRISPR–Cas systems provide adaptive immunity in prokaryotes by targeting and degrading invasive genetic elements. Among them, the Type I-F2 system represents the most compact Type I CRISPR–Cas variant, distinguished by the complete absence of both large (Cas8) and small (Cas11) subunits. In other Type I systems, Cas8 is essential for protospacer adjacent motif (PAM) recognition and for triggering Cas3 recruitment, while Cas11 stabilizes the Cascade backbone and guides the nontarget DNA strand during R-loop formation. To elucidate how I-F2 executes interference in their absence, we determined the cryo-electron microscopy structure of the I-F2 Cascade bound to target DNA and Cas3. Our structure reveals that Cas5 alone mediates PAM sensing, while Cas7 subunits directly recruit Cas3, which adopts a helicase-loaded conformation compatible with DNA engagement. We show how the helicase and C-terminal domains of Cas3 capture the displaced nontarget strand to initiate directional unwinding and degradation. These findings uncover key mechanistic adaptations that enable efficient interference without canonical large and small subunits and emphasize the mechanistic diversity among closely related Type I systems, including I-E, I-F1, and I-F2. These insights provide a structural basis for engineering the hypercompact I-F2 system for genome editing and biotechnological applications.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://epublications.vu.lt/object/elaba:279338142/279338142.pdf; https://repository.vu.lt/VU:ELABAPDB279338142&prefLang=en_US
Availability: https://repository.vu.lt/VU:ELABAPDB279338142&prefLang=en_US
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.4F6DA0D6
Database: BASE