Engineering transposon-associated TnpB-1 ωRNA system for efficient gene editing and disease treatment in mouse
Li, Z.; Guo, R.; Sun, X.; Li, G.; Liu, Y.; Huo, X.; Yang, R.; Shao, Z.; Zhang, H.; Zhang, W.; Zhang, X.; Ma, S.; Yao, Y.; Liu, X.; Yang, H.; Hu, C.; Zhou, Y.; Xu, C.
Show abstract
Transposon-associated ribonucleoprotein TnpB is known to be the ancestry endonuclease of diverse Cas12 effector proteins from type-V CRISPR system. Given its small size (409 aa), it is of interest to examine whether engineered TnpB could be used for efficient mammalian genome editing. Here, we showed that the gene editing activity of native TnpB in mouse embryos was already higher than previously identified small-sized Cas12f1. Further stepwise engineering of noncoding RNA ({omega}RNA or reRNA) component of TnpB significantly elevated the nuclease activity of TnpB. Notably, an optimized TnpB-{omega}RNA system could be efficiently delivered in vivo with single adeno-associated virus (AAV) and prevented the disease phenotype in a tyrosinaemia mouse model. Thus, the engineered miniature TnpB system represents a new addition to the current genome editing toolbox, with the unique feature of the smallest effector size that facilitate efficient AAV delivery for editing of cells and tissues.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.