Adenovirus vector technology: An efficient method for constructing recombinant adenovirus and on/off switching of gene expression

Pediatrics International

Volumn 38, Issue 2, 1996, Pages 182-188

  Kanegae, Yumi ^a   Miyake, Sanae ^a   Sato, Yumi ^a   Lee, Gwang ^a   Saito, Izumu ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

Adenovirus vector; Cre recombinase; Gene therapy

Indexed keywords

RECOMBINASE; VIRUS DNA; VIRUS PROTEIN; VIRUS VECTOR;

ADENOVIRUS; ANIMAL CELL; DNA PROTEIN COMPLEX; GENE ACTIVATION; GENE EXPRESSION; GENE STRUCTURE; GENE THERAPY; NONHUMAN; PRIORITY JOURNAL; RECOMBINANT DNA TECHNOLOGY; REPORTER GENE; REVIEW; TECHNIQUE; VIRUS RECOMBINANT;

ADENOVIRIDAE; ANIMALS; BASE SEQUENCE; DNA NUCLEOTIDYLTRANSFERASES; GENE EXPRESSION; GENE THERAPY; GENES, SWITCH; GENETIC VECTORS; INTEGRASES; MOLECULAR SEQUENCE DATA; PLASMIDS; RECOMBINATION, GENETIC; VIRAL PROTEINS;

EID: 0029966617     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.1996.tb03466.x     Document Type: Article

References (22)

1. Zabner J., Couture LA, Gregory RJ, Graham SM, Smith AE, Welsh MJ. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. Cell 1993; 75: 207–16.
2. Crystal RG, McElvaney NG, Rosenfeld MA et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis. Nature Genet. 1994; 8: 42–51.
3. Chanda PK, Natuk RJ, Mason BB et al. High level expression of the envelope glycoproteins of the human immunodeficiency virus type 1 in presence of rev gene using helper-independent adenovirus type 7 recombinants. Virology 1990; 175: 535–47.
4. Le Salle Gal La G., Robert JJ, Berrard S. et al. An adenovirus vector for gene transfer into neurons and glia in the brain. Science 1993; 259: 988–90.
5. Ragot T., Vincent N., Chafey P. et al. Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice. Nature 1993; 361: 647–50.
6. Sharp PA, Moore C., Haverty JL. The infectivity of adenovirus 5 DNA-protein complex. Virology 1976; 75: 442–56.
7. Saito I., Oya Y., Yamamoto K., Yuasa T., Shimojo H. Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome. J. Virol. 1995; 54: 711–19.
8. Sauer B., Henderson N. Cre-stimulated recombination at loxP-containing DNA sequences placed into the mammalian genome. Nucleic Acids Res. 1989; 17: 147–61.
9. O'Gorman S., Fox DT, Wahl GM. Recombinase-mediated gene activation and site-specific integration in mammalian cells. Science 1991; 251: 1351–5.
10. Gu H., Marth JD, Orban PC, Mossmann H., Rajewsky K. Deletion of a DNA polymerase β gene segment in T cells using cell type-specific gene targeting. Science 1994; 265: 103–6.
11. Miyake S., Makimura M., Kanegae Y. et al. Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome. Proc. Natl Acad. Sci. USA 1996 (In Press).
12. Kanegae Y., Lee G., Sato Y. et al. Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase. Nucleic Acids Res. 1995; 23: 3816–21.
13. Saito I., Stark GR. Charomids: Cosmid vectors for efficient cloning and a mapping of large or small restriction fragments. Proc. Natl Acad. Sci. USA 1986; 83: 8664–8.
14. Jones N., Shenk T. Isolation of deletion and substitution mutants of adenovirus type 5. Cell 1978; 13: 181–8.
15. Precious B., Russell WC. Growth, purification and titration of adenovirus. In: Many BWJ (ed.). Virology: A Practical Approach. Oxford: IRL Press, 1985; 193–205.
16. Sambrook J., Fritsch EF, Maniatis T. Molecular Cloning: A Laboratory Manual, 2nd edn. Plainview, NY: Cold Spring Harbor Lab. Press, 1989.
17. Graham FL, Smiley J., Russell WC, Narin R. Characteristics of a human cell line transformed by DNA. J. Gen. Virol. 1977; 36: 59–72.
18. Stow ND. The infectivity of adenovirus genomes lacking DNA sequences from their left-hand termini. Nucleic Acids Res. 1983; 10: 5105–19.
19. Gu H., Zou Y-R, Rajewsky K. Independent control of immunoglobulin switch recombination at individual switch regions evidenced through Cre-IoxP-mediated gene targeting. Cell 1993; 73: 1155–64.
20. Niwa H., Yamamura K., Miyazaki J. Efficient selection for high-expression transfectants with a novel eukaryotic vector Gene 1991; 108: 193–200.
21. Bett AJ, Haddara W., Prevec L., Graham FL. An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3. Proc. Natl Acad. Sci. USA 1994; 91: 8802–6.
22. Ketner G., Spencer F., Tugendreich S., Connelly C., Hieter P. Efficient manipulation of the human adenovirus genome as an infectious yeast artificial chromosome clone. Proc. Natl Acad. Sci. USA 1994; 91: 6186–90.