High-fidelity correction of mutations at multiple chromosomal positions by adeno-associated virus vectors

Journal of Virology

Volumn 73, Issue 9, 1999, Pages 7376-7380

  Inoue, Naoki ^a,b   Hirata, Roli K ^a   Russell, David W ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b CENTERS FOR DISEASE CONTROL AND PREVENTION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; VIRUS VECTOR;

ADENO ASSOCIATED VIRUS; ARTICLE; CHROMOSOME; DNA MODIFICATION; DNA REPAIR; GENE MUTATION; GENE STRUCTURE; GENE TARGETING; HUMAN; HUMAN CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0032874343     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/jvi.73.9.7376-7380.1999     Document Type: Article

References (20)

1. Bertran, J., J. L. Miller, Y. Yang, A. Fenimore Justman, F. Rueda, E. F. Vanin, and A. W. Nienhuis. 1996. Recombinant adeno-associated virus-mediated high-efficiency, transient expression of the murine cationic amino acid transporter (ecotropic retroviral receptor) permits stable transduction of human HeLa cells by ecotropic retroviral vectors. J. Virol. 70:6759-6766.
2. Brown, J. P., W. Wei, and J. M. Sedivy. 1997. Bypass of senescence after disruption of p21CIP1/WAF1 gene in normal diploid human fibroblasts. Science 277:831-834.
3. Brown, P. O. 1990. Integration of retroviral DNA. Curr. Top. Microbiol. Immunol. 157:19-48.
4. Doetschman, T., N. Maeda, and O. Smithies. 1988. Targeted mutation of the Hprt gene in mouse embryonic stem cells. Proc. Natl. Acad. Sci. USA 85:8583-8587.
5. Fujita, A., K. Sakagami, Y. Kanegae, I. Saito, and I. Kobayashi. 1995. Gene targeting with a replication-defective adenovirus vector. J. Virol. 69:6180-6190.
6. Hicks, G. G., E. G. Shi, X. M. Li, C. H. Li, M. Pawlak, and H. E. Ruley. 1997. Functional genomics in mice by tagged sequence mutagenesis. Nat. Genet. 16:338-344.
7. Inoue, N., and D. W. Russell. 1998. Packaging cells based on inducible gene amplification for the production of adeno-associated virus vectors. J. Virol. 72:7024-7031.
8. Kunkel, T. A., J. D. Roberts, and R. A. Zakour. 1987. Rapid and efficient site-specific mutagenesis without phenotypic selection. Methods Enzymol. 154:367-382.
9. Miller, A. D., J. V. Garcia, N. von Suhr, C. M. Lynch, C. Wilson, and M. V. Eiden. 1991. Construction and properties of retrovirus packaging cells based on gibbon ape leukemia virus. J. Virol. 65:2220-2224.
10. Muzyczka, N. 1992. Use of adeno-associated virus as a general transduction vector for mammalian cells. Curr. Top. Microbiol. Immunol. 158:97-129.
11. Rasheed, S., W. A. Nelson Rees, E. M. Toth, P. Arnstein, and M. B. Gardner. 1974. Characterization of a newly derived human sarcoma cell line (HT-1080). Cancer 33:1027-1033.
12. Russell, D. W., and R. K. Hirata. 1998. Human gene targeting by viral vectors. Nat. Genet. 18:325-330.
13. Rutledge, E. A., and D. W. Russell. 1997. Adeno-associated virus vector integration junctions. J. Virol. 71:8429-8436.
14. Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
15. Sandmeyer, S. B., L. J. Hansen, and D. L. Chalker. 1990. Integration specificity of retrotransposons and retroviruses. Annu. Rev. Genet. 24:491-518.
16. Thomas, K. R., C. Deng, and M. R. Capecchi. 1992. High-fidelity gene targeting in embryonic stem cells by using sequence replacement vectors. Mol. Cell. Biol. 12:2919-2923.
17. Williams, S. R., F. C. Ousley, L. J. Vitez, and R. B. DuBridge. 1994. Rapid detection of homologous recombinants in nontransformed human cells. Proc. Natl. Acad. Sci. USA 91:11943-11947.
18. Withers Ward, E. S., Y. Kitamura, J. P. Barnes, and J. M. Coffin. 1994. Distribution of targets for avian retrovirus DNA integration in vivo. Genes Dev. 8:1473-1487.
19. Yáñez, R. J., and A. C. Porter. 1998. Therapeutic gene targeting. Gene Ther. 5:149-159.
20. Yang, C. C., X. Xiao, X. Zhu, D. C. Ansardi, N. D. Epstein, M. R. Frey, A. G. Matera, and R. J. Samulski. 1997. Cellular recombination pathways and viral terminal repeat hairpin structures are sufficient for adeno-associated virus integration in vivo and in vitro. J. Virol. 71:9231-9247.