| Literature DB >> 17005721 |
Sareina Chiung-Yuan Wu1, Yaa-Jyuhn James Meir, Craig J Coates, Alfred M Handler, Pawel Pelczar, Stefan Moisyadi, Joseph M Kaminski.
Abstract
A nonviral vector for highly efficient site-specific integration would be desirable for many applications in transgenesis, including gene therapy. In this study we directly compared the genomic integration efficiencies of piggyBac, hyperactive Sleeping Beauty (SB11), Tol2, and Mos1 in four mammalian cell lines. piggyBac demonstrated significantly higher transposition activity in all cell lines whereas Mos1 had no activity. Furthermore, piggyBac transposase coupled to the GAL4 DNA-binding domain retains transposition activity whereas similarly manipulated gene products of Tol2 and SB11 were inactive. The high transposition activity of piggyBac and the flexibility for molecular modification of its transposase suggest the possibility of using it routinely for mammalian transgenesis.Entities:
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Year: 2006 PMID: 17005721 PMCID: PMC1622771 DOI: 10.1073/pnas.0606979103
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205