Programmable multistep CRISPR gene activation via control of RNA polymerase III termination
- Anupama K. Puppala
- Andrew C. Nielsen
- Maureen Regan
- Georgina E. Mancinelli
- Renee F. De Pooter
- Stephen Arnovitz
- Caspian Harding
- Michaele McGregor
- Nikolas G. Balanis
- Ryan Clarke
- Bradley J. Merrill
2025-12-05
Although genomes encode instructions for mammalian cell differentiation with rich syntactic relationships, existing methods for genetically programming cells have only modest capabilities for stepwise gene regulation. Here, we develop a sequential genetic system that transcriptionally activates endogenous genes in a preprogrammed, stepwise manner. This system uses the removal of an RNA polymerase III termination sequence to trigger both the transcriptional activation and DNA endonuclease activities of a Cas9-VPR protein, driving progression through a cascade of gene activation events. The system’s functionality in human cells, including iPSCs, enables the development of a path for cellular programming by controlling the sequential order of gene activation to influence cellular states.