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  • Viral Transfer Technology
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A binary adenoviral vector system for expressing high levels of the proapoptotic gene bax

Abstract

The bax gene plays a critical role in signaling apoptosis and expression through gene transfer may be valuable in the treatment of a variety of apoptosis-related diseases such as cancer. However, constructing an adenoviral vector expressing a bax gene driven by a constitutive promoter has been difficult, presumably because of the gene's high proapoptotic activity. Here we report a system that induces the expression of the bax gene safely by adenovirus-mediated gene cotransfer. Briefly, the system involves an adenoviral vector containing a human bax cDNA driven by a synthetic promoter consisting of five GAL4-binding sites and a TATA box (GT). This vector expresses a minimal background level of bax protein in cultured mammalian cells thus preventing apoptosis of packaging cells, however, expression of the bax gene can be induced substantially in vitro and in vivo by transferring it into target cells along with an adenoviral vector expressing the transactivator, fusion protein GAL4/VP16. Extensive apoptosis was observed after induction of the bax gene both in cultured human lung carcinoma cells and in the livers of Balb/c mice. Our results suggest that this GAL4 gene regulatory system provides an alternative approach to constructing viral vectors that express potentially toxic genes.

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References

  1. Kovesdi I et al. Adenoviral vectors for gene transfer Curr Opin Biotech 1997 8: 583–589

    Article  CAS  PubMed  Google Scholar 

  2. Yeh P, Perricaudet M . Advances in adenoviral vectors: from genetic engineering to their biology FASEB J 1997 11: 615–623

    Article  CAS  PubMed  Google Scholar 

  3. Larregina AT et al. FasL induces Fas/Apol-mediated apoptosis in human embryonic kidney 293 cells routinely used to generate E1-deleted adenoviral vectors Gene Therapy 1998 5: 563–568

    Article  CAS  PubMed  Google Scholar 

  4. Arai H, Gordon D, Nabel EG, Nabel GJ . Gene transfer of Fas ligand induces tumor regression in vivo Proc Natl Acad Sci USA 1997 94: 13862–13867

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Okuyama T et al. Efficient Fas-ligand gene expression in rodent liver after intravenous injection of a recombinant adenovirus by the use of a Cre-mediated switching system Gene Therapy 1998 5: 1047–1053

    Article  CAS  PubMed  Google Scholar 

  6. Shinoura N et al. Construction, propagation, and titer estimation of recombinant adenoviruses carrying proapoptotic genes Hum Gene Ther 1998 9: 2683–2689

    Article  CAS  PubMed  Google Scholar 

  7. Apte SS, Mattei MG, Olsen BR . Mapping of the human BAX gene to chromosome 19q13.3-q13.4 and isolation of a novel alternatively spliced transcript, BAX delta Genomics 1995 26: 592–594

    Article  CAS  PubMed  Google Scholar 

  8. Oltvai ZN, Milliman CL, Korsmeyer SJ . Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death Cell 1993 74: 609–619

    Article  CAS  PubMed  Google Scholar 

  9. Coll JL et al. Antitumor activity of bax and p53 naked gene transfer in lung cancer: in vitro and in vivo analysis Hum Gene Ther 1998 9: 2063–2074

    Article  CAS  PubMed  Google Scholar 

  10. Fang B, Ji L, Bouvet M, Roth JA . Evaluation of GAL4/TATA in vivo. Induction of transgene expression by adenovirally mediated gene codelivery J Biol Chem 1998 273: 4972–4975

    Article  CAS  PubMed  Google Scholar 

  11. Zhang WW et al. Generation and identification of recombinant adenovirus by liposome-mediated transfection and PCR analysis Biotechniques 1993 15: 868–872

    CAS  PubMed  Google Scholar 

  12. Fueyo J et al. Overexpression of E2F-1 in glioma triggers apoptosis and suppresses tumor growth in vitro and in vivo Nature Med 1998 4: 685–690

    Article  CAS  PubMed  Google Scholar 

  13. Tewari M et al. Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly (ADP-ribose) polymerase Cell 1995 81: 801–809

    Article  CAS  PubMed  Google Scholar 

  14. Lieber A et al. The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors J Virol 1997 71: 8798–8807

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Yang Y et al. Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy Proc Natl Acad Sci USA 1994 91: 4407–4411

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We thank Jude Richard for editorial review and Monica Contreras for assistance in preparing this manuscript. This study was funded by a grant from The University of Texas Physicians Referral Service, an NIH grant for a Specialized Program of Research Excellence (SPORE) in Lung Cancer (P50–CA70907), and an NIH Core Grant for DNA sequencing (CA 16672).

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Kagawa, S., Pearson, S., Ji, L. et al. A binary adenoviral vector system for expressing high levels of the proapoptotic gene bax. Gene Ther 7, 75–79 (2000). https://doi.org/10.1038/sj.gt.3301048

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