Nickase fidelity drives EvolvR-mediated diversification in mammalian cells

Juan E. Hurtado, Adam J. Schieferecke, Shakked O. Halperin, John Guan, Dylan Aidlen, David V. Schaffer () and John E. Dueber ()
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Juan E. Hurtado: Berkeley
Adam J. Schieferecke: Berkeley
Shakked O. Halperin: Berkeley
John Guan: Berkeley
Dylan Aidlen: Berkeley
David V. Schaffer: Berkeley
John E. Dueber: Berkeley

Nature Communications, 2025, vol. 16, issue 1, 1-13

Abstract: Abstract In vivo genetic diversifiers have previously enabled efficient searches of genetic variant fitness landscapes for continuous directed evolution. However, existing genomic diversification modalities for mammalian genomic loci exclusively rely on deaminases to generate transition mutations within target loci, forfeiting access to most missense mutations. Here, we engineer CRISPR-guided error-prone DNA polymerases (EvolvR) to diversify all four nucleotides within genomic loci in mammalian cells. We demonstrate that EvolvR generates both transition and transversion mutations throughout a mutation window of at least 40 bp and implement EvolvR to evolve previously unreported drug-resistant MAP2K1 variants via substitutions not achievable with deaminases. Moreover, we discover that the nickase’s mismatch tolerance limits EvolvR’s mutation window and substitution biases in a gRNA-specific fashion. To compensate for gRNA-to-gRNA variability in mutagenesis, we maximize the number of gRNA target sequences by incorporating a PAM-flexible nickase into EvolvR. Finally, we find a strong correlation between predicted free energy changes underlying R-loop formation and EvolvR’s performance using a given gRNA. The EvolvR system diversifies all four nucleotides to enable the evolution of mammalian cells, while nuclease and gRNA-specific properties underlying nickase fidelity can be engineered to further enhance EvolvR’s mutation rates.

Date: 2025
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DOI: 10.1038/s41467-025-58414-0

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