PT  - JOURNAL ARTICLE
AU  - Janice S. Chen
AU  - Yavuz S. Dagdas
AU  - Benjamin P. Kleinstiver
AU  - Moira M. Welch
AU  - Lucas B. Harrington
AU  - Samuel H. Sternberg
AU  - J. Keith Joung
AU  - Ahmet Yildiz
AU  - Jennifer A. Doudna
TI  - Enhanced proofreading governs CRISPR-Cas9 targeting accuracy
AID  - 10.1101/160036
DP  - 2017 Jan 01
TA  - bioRxiv
PG  - 160036
4099  - http://biorxiv.org/content/early/2017/07/06/160036.short
4100  - http://biorxiv.org/content/early/2017/07/06/160036.full
AB  - The RNA-guided CRISPR-Cas9 nuclease from Streptococcus pyogenes (SpCas9) has been widely repurposed for genome editing1–4. High-fidelity (SpCas9-HF1) and enhanced specificity (eSpCas9(1.1)) variants exhibit substantially reduced off-target cleavage in human cells, but the mechanism of target discrimination and the potential to further improve fidelity were unknown5–9. Using single-molecule Förster resonance energy transfer (smFRET) experiments, we show that both SpCas9-HF1 and eSpCas9(1.1) are trapped in an inactive state10 when bound to mismatched targets. We find that a non-catalytic domain within Cas9, REC3, recognizes target mismatches and governs the HNH nuclease to regulate overall catalytic competence. Exploiting this observation, we identified residues within REC3 involved in mismatch sensing and designed a new hyper-accurate Cas9 variant (HypaCas9) that retains robust on-target activity in human cells. These results offer a more comprehensive model to rationalize and modify the balance between target recognition and nuclease activation for precision genome editing.