Expanding plant genome-editing scope by an engineered iSpyMacCas9 system that targets A-rich PAM sequences

The most popular CRISPR-SpCas9 system recognizes canonical NGG protospacer adjacent motifs (PAMs). Previously engineered SpCas9 variants, such as Cas9-NG, favor G-rich PAMs in genome editing. In this manuscript, we describe a new plant genome-editing system based on a hybrid iSpyMacCas9 platform that allows for targeted mutagenesis, C to T base editing, and A to G base editing at A-rich PAMs. This study fills a major technology gap in the CRISPR-Cas9 system for editing NAAR PAMs in plants, which greatly expands the targeting scope of CRISPR-Cas9. Finally, our vector systems are fully compatible with Gateway cloning and will work with all existing single-guide RNA expression systems, facilitating easy adoption of the systems by others. We anticipate that more tools, such as prime editing, homology-directed repair, CRISPR interference, and CRISPR activation, will be further developed based on our promising iSpyMacCas9 platform.

Automated summary

This study presents a new plant genome-editing system based on the hybrid iSpyMacCas9 platform, allowing for targeted mutagenesis and base editing at A-rich PAMs. It fills a significant technology gap in the CRISPR-Cas9 system for editing NAAR PAMs in plants, greatly expanding the targeting scope of CRISPR-Cas9. The vector systems are fully compatible with Gateway cloning and existing single-guide RNA expression systems, making it easy for others to adopt.