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Journal of Virology, May 2000, p. 4612-4620, Vol. 74, No. 10
Division of Hematology, Department of
Medicine, and Markey Molecular Medicine Center, University of
Washington, Seattle, Washington 98195-7720
Received 23 November 1999/Accepted 21 February 2000
Adeno-associated virus (AAV) vectors can transduce cells by several
mechanisms, including (i) gene addition by chromosomal integration or
episomal transgene expression or (ii) gene targeting by modification of
homologous chromosomal sequences. The latter process can be used to
correct a variety of mutations in chromosomal genes with high fidelity
and specificity. In this study, we used retroviral vectors to introduce
mutant alkaline phosphatase reporter genes into normal human cells and
subsequently corrected these mutations with AAV gene targeting vectors.
We find that increasing the length of homology between the AAV vector
and the target locus improves gene correction rates, as does
positioning the mutation to be corrected in the center of the AAV
vector genome. AAV-mediated gene targeting increases with time and
multiplicity of infection, similar to AAV-mediated gene addition.
However, in contrast to gene addition, genotoxic stress did not affect
gene targeting rates, suggesting that different cellular factors are
involved. In the course of these studies, we found that (i) vector
genomes less than half of wild-type size could be packaged as monomers or dimers and (ii) packaged dimers consist of inverted repeats with
covalently closed hairpins at either end. These studies should prove
helpful in designing AAV gene targeting vectors for basic research or
gene therapy.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Design and Packaging of Adeno-Associated Virus Gene
Targeting Vectors
*
Corresponding author. Mailing address: Division of
Hematology and Markey Molecular Medicine Center, University of
Washington, Box 357720, Seattle, WA 98195. Phone: (206) 616-4562. Fax:
(206) 616-8298. E-mail: drussell{at}u.washington.edu.
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