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Production of Human Tissue Plasminogen Activator in Transgenic Mouse Milk

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Abstract

We set out to express an exogenous gene in the mammary epithelium of transgenic mice in the hope that the encoded protein would be secreted into milk. The promoter and upstream regulatory sequences from the murine whey acid protein (WAP) gene were fused to cDNA encoding human tissue plasminogen activator (t–PA) with its endogenous secretion signal sequence. This hybrid gene was injected into mouse embryos, resultant transgenic mice were mated, and milk obtained from lactating females was shown to contain biologically active t–PA. This result establishes the feasibility of secretion into the milk of transgenic animals for production of biologically active heterologous proteins, and may provide a powerful method to produce such proteins on a large scale.

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References

  1. Gordon, K. and Ruddle, F.H. 1986. Gene transfer into mouse embryos. In: Development Biology. Gwatkin, R. B. L. (ed.) Plenum Publishing Corp., New York. 4: 1–36.

    Google Scholar 

  2. Palmiter, R.D. and Brinster, R.L. 1986. Germ-line transformation of mice. Ann. Rev. Genet. 20: 465–499.

    Article  CAS  Google Scholar 

  3. Hennighausen, L.G. and Sippel, A.E. 1982. Characterization and cloning of the mRNAs specific for the lactating mouse mammary gland. Eur. J. Biochem. 125: 131–141.

    Article  CAS  Google Scholar 

  4. Hobbs, A.A., Richards, D.A., Kessler, D.J., and Rosen, J.M. 1982. Complex hormonal regulation of rat casein gene expression. J. Biol. Chem. 257: 3598–3605.

    CAS  Google Scholar 

  5. Richards, D.A., Rodgers, J.R., Supowit, S.C., and Rosen, J.M. 1981. Construction and preliminary characterization of the rat casein and lactalbumin cDNA clones. J. Biol. Chem. 256: 526–532.

    CAS  PubMed  Google Scholar 

  6. Hennighausen, L.G., Sippel, A.E., Hobbs, A.A., and Rosen, J.M. 1982. Comparative sequence analysis of mRNAs coding for mouse and rat whey acid protein. Nucleic Acids Res. 10: 3732–3744.

    Google Scholar 

  7. Lubon, H. and Hennighausen, L. 1987. Nuclear proteins from lactating mammary glands bind to the promoter of a milk protein gene. Nuc. Acids Res. 15: 2103–2121.

    Article  CAS  Google Scholar 

  8. Hennighausen, L.G. and Sippel, A.E. 1982. Mouse whey acidic protein is a mouse member of the family of four “disulfide core” proteins. Nucleic Acids Res. 10: 2677–2684.

    Article  CAS  Google Scholar 

  9. Campbell, S.M., Rosen, J.M., Hennighausen, L., Strech-Jurk, U., and Sippel, A.E. 1984. Comparison of the whey acidic protein genes of the rat and mouse. Nucleic Acids Res. 12: 8685–8696.

    Article  CAS  Google Scholar 

  10. Andres, A.-C., Schonenberger, C.-A., Groner, B., Hennighausen, L., LeMeur, M., and Gerlinger, P. 1987. Ha-ras oncogene expression directed by a milk protein gene promoter: tissue specificity, hormonal regulation, and tumor induction in transgenic mice. Proc. Natl. Acad. Sci. USA 84: 1299–1303.

    Article  CAS  Google Scholar 

  11. Reddy, V.B., Garramone, A.J., Sasak, H., Wei, C.-M., Watkins, P., Galli, J., and Hsuing, N. 1987. Expression of human uterine tissue-type plasminogen activator in mouse cells using BPV vectors. DNA, in press.

  12. Craig, R.K., Perera, P.A.J., Mellor, A., and Smith, A. 1979. Initiation and processing in vitro of the primary translation products of guineapig caseins. Biochem. J. 184: 261–267.

    Article  CAS  Google Scholar 

  13. Ossowski, L., Biegel, D., and Reich, E. 1979. Mammary plasminogen activator: correlation with involution, hormonal modulation and comparison between normal and neoplastic tissue. Cell 16: 929–940.

    Article  CAS  Google Scholar 

  14. Busby, S.J., Bailey, M.C., Mulvihill, E.R., Joseph, M.L., and Kumar, A.A. 1986. Expression of human tissue plasminogen activator in transgenic mice. American Heart Assn. 74: II–247a.

    Google Scholar 

  15. Choo, K.H., Raphael, K., McAdam, W., and Peterson, M.G. 1987. Expression of active human blood clotting factor IX in transgenic mice: use of cDNA with complete mRNA sequence. Nuc. Acids Res. 15: 871–884.

    Article  CAS  Google Scholar 

  16. Hammer, R.E., Pursel, V.G., Rexroad, C.E., Wall, R.J., Bolt, D.J., Ebert, K.M., Palmiter, R.D., and Brinster, R.L. 1985. Production of transgenic rabbits, sheep and pigs by microinjection. Nature 315: 680–683.

    Article  CAS  Google Scholar 

  17. Yang, R.C.-A., Lis, J., and Wu, R. 1979. Elution of DNA from agarose gels after electrophoresis. Meth. in Enz. 68: 176–182.

    CAS  Google Scholar 

  18. Overbeek, P.A., Chepelinsky, A.B., Khillan, J.S., Piatiagorsky, J., and Westphal, H. 1985. Lens-specific expression and developmental regulation of the bacterial chloramphenicol acetyltransferase gene driven by the murine α-A crystallin promoter in transgenic mice. Proc. Natl. Acad. Sci. USA 82: 7815–7819.

    Article  CAS  Google Scholar 

  19. Hsiung, M., Fitts, R., Wilson, S., Milne, A., and Hamer, D. 1984. Efficient production of hepatitis B surface antigen using a bovine papilloma virus-metallothionein vector. Jour. Mol. and Appl. Genet. 2: 497–506.

    CAS  Google Scholar 

  20. Granelli-Piperno, A. and Reich, E.J. 1978. A study of proteases and protease inhibitor complexes in biological fluids. J. Exp. Med. 148: 223–234.

    Article  CAS  Google Scholar 

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Gordon, K., Lee, E., Vitale, J. et al. Production of Human Tissue Plasminogen Activator in Transgenic Mouse Milk. Nat Biotechnol 5, 1183–1187 (1987). https://doi.org/10.1038/nbt1187-1183

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  • DOI: https://doi.org/10.1038/nbt1187-1183

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