Source  Plant Communications

Published  May 19, 2026

DOI: 10.1016/j.xplc.2026.101921

IF 11.6

Abstract  Multiplex genome editing enables the simultaneous modification of multiple genomic loci, which is essential for understanding gene networks and engineering complex traits in crops. However, achieving high editing efficiency across multiple targets is a significant challenge. To address this, we present an optimized CRISPR system for rice that combines a monomeric TREX2-SpCas9 fusion with a novel array of tRNA-based gRNA processing elements. The TREX2-SpCas9 fusion significantly enhances editing performance, resulting in higher efficiency, larger deletions, and increased compared to wild-type SpCas9 and other exonuclease fusions. By systematic evaluating 38 endogenous ricetRNAgenes, we identified 13 high-performing candidates (e.g., tRNALeu-1and tRNAPro-1) that outperformed the widely used tRNAGlyand tRNAMet, enabling highly efficient processing of multiplexed gRNA arrays. Incorporating these top-performing tRNAs into our system enabled simultaneous editing of up to 29OsCPKgenes in a single rice plant. Furthermore, we demonstrated the cross-species applicability of this platform in the dicotNicotiana benthamianathrough transient expression, where the rice-derived tRNA elements facilitated high-efficiency editing. This optimized multiplex gene editing system provides a robust, scalable platform for accelerating plant functional genomics and improving complex agronomic traits.