Cell genomicsOct 17, 2025

How the structure and function of F. rodentium Cas9 help improve CRISPR-Cas proteins

CRISPR Gene Editing Weekly Brief ↗PubMed ↗DOI ↗

Updated Jan 3, 2026

Abstract

The Faecalibaculum rodentium CRISPR-Cas9 system shows enhanced gene-editing precision and efficiency compared to SpCas9.

Cryo-electron microscopy structures reveal the FrCas9-sgRNA-DNA complex in two distinct states.
FrCas9 specializes in recognizing the 5'-NRTA-3' protospacer adjacent motif (PAM).
The phosphate lock loop is crucial for adjusting FrCas9's off-target sensitivity and catalytic efficiency.
Targeted changes in the phosphate lock loop and PAM-distal region can improve both editing precision and efficiency.

Simplified

The Faecalibaculum rodentium (Fr) CRISPR-Cas9 system exhibits enhanced gene-editing precision and efficiency compared to SpCas9, with distinctive advantages in targeting the TATA box in eukaryotic promoters. However, the underlying molecular mechanisms remained unexplored. Here, we present cryo-electron microscopy structures of the FrCas9-single guide RNA (sgRNA)-DNA complex in both the R-loop expansion and pre-catalytic states, shedding light on its specialized recognition of the 5'-NRTA-3' protospacer adjacent motif (PAM) and the unusual overwinding of the sgRNA-DNA heteroduplex. Our investigations into the structure and extensive mutational analyses reveal that the phosphate lock loop plays a pivotal role in finely adjusting FrCas9's off-target sensitivity and catalytic efficiency. Remarkably, targeted residue substitutions in the phosphate lock loop and the PAM-distal region were found to synergistically enhance both the editing precision and efficiency of FrCas9. These findings advance our understanding of Cas9's accuracy and potency mechanisms while providing a molecular foundation for the rational design and development of next-generation CRISPR technologies.

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Funding

Competing interests

Declaration of interests R.T. is an employee of Generulor Co., Ltd.

PubMed

How the structure and function of F. rodentium Cas9 help improve CRISPR-Cas proteins

Abstract

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Abstract

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Related papers

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