piggyBac transposase tools for genome engineering

• Published in: Proceedings of the National Academy of Sciences - PNAS 2013-06, Vol.110 (25), p.E2279-E2287
• Main Authors: Li, Xianghong, Burnight, Erin R, Cooney, Ashley L, Malani, Nirav, Brady, Troy, Sander, Jeffry D, Staber, Janice, Wheelan, Sarah J, Joung, J Keith, McCray, Jr, Paul B, Bushman, Frederic D, Sinn, Patrick L, Craig, Nancy L
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Binding sites; Biological Sciences; Deoxyribonucleic acid; DNA; DNA Transposable Elements - genetics; Gene Transfer Techniques; Genetic engineering; Genetic Engineering - methods; Genome, Human - genetics; Genotype & phenotype; HEK293 Cells; HeLa Cells; Humans; Mammals; Molecular Sequence Data; Mutagenesis, Insertional - methods; Nerve Tissue Proteins - genetics; Pluripotent Stem Cells - cytology; Pluripotent Stem Cells - physiology; PNAS Plus; Proteins; Saccharomyces cerevisiae - genetics; Stem cells; Zinc Fingers - genetics
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1305987110

The transposon piggyBac is being used increasingly for genetic studies. Here, we describe modified versions of piggyBac transposase that have potentially wide-ranging applications, such as reversible transgenesis and modified targeting of insertions. piggyBac is distinguished by its ability to excise precisely, restoring the donor site to its pretransposon state. This characteristic makes piggyBac useful for reversible transgenesis, a potentially valuable feature when generating induced pluripotent stem cells without permanent alterations to genomic sequence. To avoid further genome modification following piggyBac excision by reintegration, we generated an excision competent/integration defective (Exc ⁺Int ⁻) transposase. Our findings also suggest the position of a target DNA–transposase interaction. Another goal of genome engineering is to develop reagents that can guide transgenes to preferred genomic regions. Others have shown that piggyBac transposase can be active when fused to a heterologous DNA-binding domain. An Exc ⁺Int ⁻ transposase, the intrinsic targeting of which is defective, might also be a useful intermediate in generating a transposase whose integration activity could be rescued and redirected by fusion to a site-specific DNA-binding domain. We show that fusion to two designed zinc finger proteins rescued the Int ⁻ phenotype. Successful guided transgene integration into genomic DNA would have broad applications to gene therapy and molecular genetics. Thus, an Exc ⁺Int ⁻ transposase is a potentially useful reagent for genome engineering and provides insight into the mechanism of transposase–target DNA interaction.