Integrating DNA delivery systems hold promise for many applications including treatment of diseases; however， targeted integration is needed for improved safety. The piggyBac (PB) transposon system is a highly active non-viral gene delivery system capable of integrating defined DNA segments into host chromosomes without requiring homologous recombination. We systematically compared four different engineered zinc finger proteins (ZFP)， four transcription activator-like effector proteins (TALE)， CRISPR associated protein 9 (SpCas9) and the catalytically inactive dSpCas9 protein fused to the amino-terminus of the transposase enzyme designed to target the hypoxanthine phosphoribosyltransferase (HPRT) gene loc... More
Integrating DNA delivery systems hold promise for many applications including treatment of diseases; however， targeted integration is needed for improved safety. The piggyBac (PB) transposon system is a highly active non-viral gene delivery system capable of integrating defined DNA segments into host chromosomes without requiring homologous recombination. We systematically compared four different engineered zinc finger proteins (ZFP)， four transcription activator-like effector proteins (TALE)， CRISPR associated protein 9 (SpCas9) and the catalytically inactive dSpCas9 protein fused to the amino-terminus of the transposase enzyme designed to target the hypoxanthine phosphoribosyltransferase (HPRT) gene located on human chromosome X. Chimeric transposases were evaluated for expression， transposition activity， chromatin immunoprecipitation at the target loci， and targeted knockout of the HPRT gene in human cells. One ZFP-PB and one TALE-PB chimera demonstrated notable HPRT gene targeting. In contrast， Cas9/dCas9-PB chimeras did not result in gene targeting. Instead， the HPRT locus appeared to be protected from transposon integration. Supplied separately， PB permitted highly efficient isolation of Cas9-mediated knockout of HPRT， with zero transposon integrations in HPRT by deep sequencing. In summary， these tools may allow isolation of 'targeted-only' cells， be utilized to protect a genomic locus from transposon integration， and enrich for Cas9-mutated cells.
