A TRL-3 platform using Cas12a to enable precise insertion of large DNA cassettes in soybeans and oilseed rape. The approach synchronizes donor availability with a transient repair window and uses dual-junction-dependent selection to recover cells forming both intended genomic junctions. Proposed enhancements include donor optimization for large payloads, transient repair-pathway modulation, and optional split-donor reconstitution for larger inserts, targeting higher usable plant proportions and fewer multicopy, backbone-positive, and ectopic events.
A genetic engineering platform for oilseed crops, focused on soybeans and oilseed rape. The system uses the Cas12a nuclease to enable precise insertion of large DNA cassettes, reported in the 7–10 kb range, with future capability extending to 15–25 kb. Rather than treating donor delivery, nuclease timing, and repair as separate steps, the platform synchronizes these processes to improve the efficiency and accuracy of genetic modifications. It is designed to recover cells that form both intended genomic junctions, reducing incomplete or undesirable integration events.
Currently at TRL-3, the platform is in the experimental phase and undergoing validation. Development is organized into multiple phases, including proof-of-concept studies, regeneration, inheritance testing, and payload scaling.
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