De novo engineered guide RNA-directed transposition with TnpB-family proteins
TL;DR
Estimation of how Cas12 proteins and antecedent TnpB proteins can be engineered for high performance and specificity with guide RNA-directed systems in bacteria is established.
Abstract
Summary Programmable DNA integration using CRISPR-associated transposase elements (CASTs) offer powerful capabilities for genome engineering. The large single effector Cas12k CAST examples evolved from a minimal TnpB nuclease protein. Here, we engineer a de novo RNA-guided transposition systems in bacteria, where the single guide RNA effector components are repurposed nuclease-dead TnpB-family proteins. These compact systems mediate high-efficiency guide RNA-directed DNA insertion with preserved orientation control, target immunity, release of a host factor requirement, and can be paired with an exonuclease domain to mediate cut-and-paste transposition. In this engineered context, the TnpB derivatives show features not predicted from the original enzymes suggesting untapped avenues for improvement. In parallel, we show that mutations at the TniQ-TnsC interface in the Cas12k CAST system selectively attenuate off-site insertions while enhancing on-site activity. These results establish how Cas12 proteins and antecedent TnpB proteins can be engineered for high performance and specificity with guide RNA-directed systems.