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.
MeSH Terms
Animals
CHO Cells
Cell Line
Cell Line, Tumor
Cricetinae
Cricetulus
DNA Transposable Elements/genetics,physiology
DNA-Binding Proteins/chemistry,genetics,physiology
HeLa Cells
Humans
Insect Proteins/genetics,physiology
Moths/virology
Mutagenesis, Insertional
Mutagenesis, Site-Directed
Transposases/chemistry,genetics,physiology
Chemicals
DNA Transposable Elements
DNA-Binding Proteins
Insect Proteins
mariner transposases
Transposases
sleeping beauty transposase, human
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Wu Sareina Chiung-Yuan
Cancer Research Center, Medical College of Georgia, Augusta, GA 30912, USA.
Meir Yaa-Jyuhn James
Coates Craig J
Handler Alfred M
Pelczar Pawel
Moisyadi Stefan
Kaminski Joseph M
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