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Analysis of site‐specific transgene integration following cotransduction with recombinant adeno‐associated virus and a rep encodingplasmid
Author(s) -
Huttner Nadja A.,
Girod Anne,
Schnittger Susanne,
Schoch Claudia,
Hallek Michael,
Büning Hildegard
Publication year - 2003
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.324
Subject(s) - transduction (biophysics) , transgene , biology , adeno associated virus , plasmid , microbiology and biotechnology , transfection , recombinant dna , gene , chromosome , southern blot , hela , genetics , virology , vector (molecular biology) , cell , biochemistry
Background Recombinant adeno‐associated virus (rAAV) has many advantages for gene therapeutic applications in comparison with other vector systems. One of the most promising features is the ability of wild‐type (wt) AAV to integrate site‐specifically into human chromosome 19. However, this feature is lost in rAAV vectors due to the removal of the rep ‐coding sequences. Methods HeLa cells were transfected with a rep expression plasmid, infected by rAAV and grown with or without selection pressure. Single cell clones were generated and genomic DNA was analyzed for site‐specific integration by Southern blotting analysis and fluorescence in situ hybridization (FISH). Results Transfection of HeLa cells with a rep expression plasmid followed by transduction with a rAAV vector resulted in site‐specific integration of the transgene at AAVS1 on human chromosome 19 in 7 of 10 cell clones analyzed. In marked contrast, transduction of cells with rAAV alone did not result in any site‐specific integration of the transgene. Conclusions The high frequency with which the site‐specific integration took place in the presence of Rep protein is comparable with the results observed with wtAAV. These results offer opportunities for the development of specifically integrating rAAV vectors. Copyright © 2002 John Wiley & Sons, Ltd.