Reprogramming Cas9 PAM Recognition for Allele-Specific Editing

Tartaglia, J. A.; Nguyen, V.; Desmarais, J.; Weissman, R.; Thornton, B.; Trinidad, M.; Briseno, K.; Hudson, T.; Catamura, C.; Lareau, L.; Urnov, F.; Doudna, J. A.; Savage, D.

doi:10.64898/2026.08.10.744034

bioRxiv · 10.64898/2026.08.10.744034

Reprogramming Cas9 PAM Recognition for Allele-Specific Editing

Tartaglia, J. A.·Nguyen, V.·Desmarais, J.·Weissman, R.·Thornton, B.·Trinidad, M.·Briseno, K.·Hudson, T.·Catamura, C.·Lareau, L.·Urnov, F.·Doudna, J. A.·Savage, D.

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Abstract

The therapeutic potential of CRISPR-Cas9 genome editing is fundamentally constrained by the requirement for specific short DNA sequences (PAMs) flanking the target site, limiting access to many clinically relevant genomic loci. This stringent PAM requirement is particularly problematic in applications which require precise positioning, such as base editing and allele-specific editing. Although PAM-relaxed variants have expanded the targetable genome, they incur trade-offs in on-target activity, off-target editing, and cleavage kinetics. This highlights an unmet need for variants that are re-targeted to alternative PAMs in order to maintain the specificity and enzymatic performance inherent to stringent dinucleotide PAM recognition. To overcome these limitations, we developed a yeast selection platform to engineering SpCas9 variants with re-specified PAM recognition. Using a clinically relevant Huntingtons disease gene (HTT) SNP as a proof-of-concept target, we engineered variants with reciprocal NGC and NGT PAM selectivity, as a step toward allele-specific editing in a large percentage of Huntingtons disease patients. These yeast-selected SpCas9 variants retained their modified activity across multiple endogenous HEK293T loci, demonstrating that this specificity is robust across diverse genomic contexts. The variants surpassed PAM-broadened variants on their respective on-target PAM while displaying broad loss of activity across alternative PAMs, effectively re-specifying PAM recognition toward a single dinucleotide sequence. Retargeted variants recovered on-target cleavage kinetics approaching that of wild-type SpCas9, even under competing substrate conditions, demonstrating that PAM re-specification can simultaneously restore catalytic efficiency and improve specificity. Beyond NGC and NGT, we leveraged our high-throughput platform to engineer Cas9 with re-specified activity across multiple additional non-canonical PAMs in yeast, further demonstrating its utility as a general and programmable framework for expanding the therapeutic reach of precision genome editing.

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Tartaglia, J. A., Nguyen, V., Desmarais, J., Weissman, R., Thornton, B., Trinidad, M., Briseno, K., Hudson, T., Catamura, C., Lareau, L., Urnov, F., Doudna, J. A., Savage, D.. 2026-08-11. Reprogramming Cas9 PAM Recognition for Allele-Specific Editing. https://doi.org/10.64898/2026.08.10.744034

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