RNA-guided CRISPR nuclease Cas9 cannot reliably differentiate between single nucleotide variations (SNVs) of targeted DNA sequences determined by their guide RNA (gRNA): they typically exhibit similar nuclease activities at any of those variations, unless the variation occurs with specific sequence contexts known as protospacer adjacent motifs (PAMs). Our approach, "TOP-SECRETS," generates gRNA variants that allow Cas9 ribonucleoproteins (RNPs) to reliably discriminate between healthy and disease-associated SNVs outside of PAMs.
TOP-SECRETS enables Cas9 nucleases to discriminate SNVs outside of PAMs.
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作者:Herring-Nicholas Ashley, Fisher-Huynh Stephanie, Josephs Eric A
| 期刊: | bioRxiv | 影响因子: | 0.000 |
| 时间: | 2025 | 起止号: | 2025 May 10 |
| doi: | 10.1101/2025.05.06.652491 | ||
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