Skip to main content
Log in

Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line

  • Published:
Somatic Cell and Molecular Genetics

Abstract

We are exploring the origin and function of amplified DNA sequences associated with double minutes (DMs) in a spontaneously transformed derivative of mouse 3T3 cells. Toward that goal, we have constructed a cDNA library using RNA from these cells and have isolated cDNA clones representing sequences that are amplified and overexpressed in these 3T3-DM cells. From results of Northern- and Southern-blot analyses, we conclude that these cDNAs represent two distinct genes, which we have designated mdm-1and mdm-2.Using DNAs from a panel of Chinese hamster-mouse somatic cell hybrids together with in situ hybridization protocols for gene mapping studies, we have found that these DM-associated, amplified DNA sequences originate from mouse chromosome 10, region C1–C3. Sequences homologous to mdm-1and mdm-2are present in the genomes of several species examined, including that of man.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. Bishop, J.M. (1983).Annu. Rev. Biochem. 52:301–354.

    PubMed  Google Scholar 

  2. George, D.L. (1984).Cancer Surv. 3:497–513.

    Google Scholar 

  3. Cowell, J.K. (1982).Annu. Rev. Genet. 16:21–59.

    PubMed  Google Scholar 

  4. Schwab, M., Alitalo, K., Varmus, H.E., Bishop, J.M., and George, D. (1983).Nature 303:497–501.

    PubMed  Google Scholar 

  5. Brodeur, G., Seeger, R.C., Schwab, M., Varmus, H.E., and Bishop, J.M. (1984).Science 224:1121–1124.

    PubMed  Google Scholar 

  6. Schwab, M., Alitalo, K., Klempnauer, K.-H., Varmus, H.E., Bishop, J.M., Gilbert, F., Brodeur, G., Goldstein, M., and Trent, J. (1983).Nature 305:245–248.

    PubMed  Google Scholar 

  7. Schwab, M., Ellison, J., Busch, M., Rosenau, W., Varmus, H.E., and Bishop, J.M. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:4940–4944.

    PubMed  Google Scholar 

  8. Little, C.D., Nau, M.M., Carney, D.N., Gazdar, A.F., and Minna, J.D. (1983).Nature 306:194–196.

    PubMed  Google Scholar 

  9. Nau, M.M., Brooks, B.J., Battey, J., Sausville, E., Gazdar, A.F., Kirsch, I.R., McBride, O.W., Bertness, V., Hollis, G.F., and Minna, J.D. (1985).Nature 318:69–73.

    PubMed  Google Scholar 

  10. Wong, A.J., Ruppert, J.M., Eggleston, J., Hamilton, S., Baylin, S.B., and Vogelstein, B. (1986).Science 233:461–464.

    PubMed  Google Scholar 

  11. George, D.L., and Powers, V.E. (1982). InGene Amplification, (ed.) Schimke, R. (Cold Spring Harbor Laboratory, Cold Spring Harbor, New York), pp. 199–204.

    Google Scholar 

  12. Matsuya, Y., and Green, H. (1969).Science 163:397–398.

    PubMed  Google Scholar 

  13. Dorman, B.P., Shimizu, N., and Ruddle, F. (1978).Proc. Natl. Acad. Sci. U.S.A. 75:2363–2367.

    PubMed  Google Scholar 

  14. George, D.L., and Francke, U. (1980).Cytogenet. Cell Genet. 28:217–226.

    PubMed  Google Scholar 

  15. George, D.L., and Powers, V.E. (1981).Cell 24:117–123.

    PubMed  Google Scholar 

  16. Topp, W.C. (1981).Virology 113:408–411.

    PubMed  Google Scholar 

  17. Cahilly, L.A., and George, D.L. (1985).Cytogenet. Cell Genet. 39:140–144.

    PubMed  Google Scholar 

  18. Cahilly, L.A., George, D.L., Daugherty, B.L., and Pestka, S. (1985).J. Int. Res. 5:391–395.

    Google Scholar 

  19. Aviv, H., and Leder, P. (1972).Proc. Natl. Acad. Sci. U.S.A. 69:1408–1412.

    PubMed  Google Scholar 

  20. Schwarzbauer, J., Tamkun, J.W., Lemischka, I.R., and Hynes, R.O. (1983).Cell 35:421–431.

    PubMed  Google Scholar 

  21. Gorecki, M., and Rozenblatt, S. (1980).Proc. Natl. Acad. Sci. U.S.A. 77:3686–3690.

    PubMed  Google Scholar 

  22. George, D.L., Scott, A.F., Trusko, S., Glick, B., Ford, E., and Dorney, D.J. (1985).EMBO J. 4:1199–1203.

    PubMed  Google Scholar 

  23. Singh, L., and Jones, K.W. (1984).Nucleic Acids Res. 12:5627–5638.

    PubMed  Google Scholar 

  24. Fujii, D., Brissenden, J.E., Derynck, R., and Francke, U. (1986).Somat. Cell Mol. Genet. 12:281–288.

    PubMed  Google Scholar 

  25. Feinberg, A.P., and Vogelstein, B. (1983).Anal. Biochem. 132:6–13.

    PubMed  Google Scholar 

  26. Francke, U., Lalley, P.A., Moss, W., Ivy, L., and Minna, J.D. (1977).Cytogenet. Cell Genet. 19:57–84.

    PubMed  Google Scholar 

  27. Francke, U., and Taggart, R.T. (1979).Proc. Natl. Acad. Sci. U.S.A. 76:5230–5233.

    PubMed  Google Scholar 

  28. Harper, M.E., Ullrich, A., and Saunders, G.F. (1981).Proc. Natl. Acad. Sci. U.S.A. 78:4458–4460.

    PubMed  Google Scholar 

  29. Lin, C.C., Draper, P.N., and DeBrackeleer, M. (1985).Cytogenet. Cell Genet. 39:269–274.

    PubMed  Google Scholar 

  30. Ellis, R.W., DeFeo, D., Shih, T.Y., Gonda, M.A., Young, H.A., Tsuchida, N., Lowy, D.R., and Scolnick, E.M. (1981).Nature 292:506–511.

    PubMed  Google Scholar 

  31. Sakaguchi, A.Y., Lalley, P.A., Zabel, B.U., Ellis, R.W., Scolnick, E.M., and Naylor, S.L. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:525–529.

    PubMed  Google Scholar 

  32. Nesbitt, M.N., and Francke, U. (1973).Chromosoma 41:145–158.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cahilly-Snyder, L., Yang-Feng, T., Francke, U. et al. Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line. Somat Cell Mol Genet 13, 235–244 (1987). https://doi.org/10.1007/BF01535205

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01535205

Keywords

Navigation