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DNA of simian virus 40 mutates Chinese hamster cells

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Summary

Infection of Chinese hamster cells with SV40 DNA gives rise to mutants resistant both to 8-azaguanine (AG) and aminopterin (AP). This mutagenic effect can be raised when facilitating DNA uptake of cells by a helper agent. The extent of mutagenic action depends further on the concentration of DNA applied to the cells, with 2 µg/ml being more effective than 10 µg/ml, as well as on the period of incubation of infected cells before onset of mutant selection (mutation expression time). Using the AG resistance marker the mutation frequency can be increased more than 8-fold compared with the spontaneous mutation frequency. Reconstituted SV 40 minichromosomes show a mutagenic action which is similar to the DNA-mediated mutagenesis whereas non-viral DNA from mammalian cells fails to induce mutations significantly. A major part of isolated clones of SV 40-induced mutants tested so far does express SV 40 T-antigen, suggesting the persistence of SV 40 genetic material in these clones. The possible existence of relations between mutagenic and transforming capacities of SV 40 is discussed.

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References

  1. Abbondandolo, A., Bonatti, S., Coletta, C., Corti, G., Matteucci, F., Mazzaccaro, A., Rainaldi, G.: A comparative study of different experimental protocols for mutagenesis assays with the 8-azaguanine resistance system in cultured Chinese hamster cells. Mutation Res.37, 293–306 (1976).

    Google Scholar 

  2. Abrahams, P. J., van der Eb, A. J.:In vitro transformation of rat and mouse cells by DNA from Simian virus 40. J. Virol.16, 206–209 (1975).

    Google Scholar 

  3. Albrecht, A. M., Biedler, J. L., Hutchison, D. J.: Two different species of dihydrofolate reductase in mammalian cells differentially resistant to amethopterin and methasquin. Cancer Res.32, 1539–1546 (1972).

    Google Scholar 

  4. Al-Moslih, M. I., Dubes, G. R.: The kinetics of DEAE-dextran induced cell sensitization to transformation. J. gen. Virol.18, 189–193 (1973).

    Google Scholar 

  5. Amati, P., Lago, C.: Sensitivity to Amphotericin B ofin vitro established cell lines. Nature247, 466–469 (1974).

    Google Scholar 

  6. Arlett, C. F., Harcourt, S. A.: Expression time and spontaneous unstability in the estimation of induced mutation frequency following treatment of Chinese hamster cells by ultraviolet light. Mutation Res.16, 301–306 (1972).

    Google Scholar 

  7. Basilico, C., Zouzias, D.: Regulation of viral transcription and tumor antigen expression in cells transformed by Simian virus 40. Proc. Nat. Acad. Sci. (Wash.)73, 1931–1935 (1976).

    Google Scholar 

  8. Bourgaux, P., Bourgaux-Ramoisy, D., Stocker, M.: Further studies on transformation by DNA from polyoma virus. Virology25, 364–371 (1965).

    Google Scholar 

  9. Caskey, C. T., Kruh, G. D.: The HPRT locus. Cell16, 1–9 (1979).

    Google Scholar 

  10. Casto, B. C., Miyagi, M., Meyers, J., DiPaolo, J. A.: Increased integration of viral genome following chemical and viral treatment of hamster embryo cells. Chem.-Biol. Interactions25, 255–269 (1979).

    Google Scholar 

  11. Chu, E. H. Y., Malling, H. V.: Mammalian cell genetics. II. Chemical induction of specific locus mutations in Chinese hamster cellsin vitro. Proc. Nat. Acad. Sci. (Wash.)61, 1306–1312 (1968).

    Google Scholar 

  12. Crawford, L. V., Cole, C. N., Smith, A. E., Paucha, E., Tegtmeyer, P., Rundell, K., Berg, P.: Organization and expression of early genes of Simian virus 40. Proc. Nat. Acad. Sci. (Wash.)75, 117–121 (1978).

    Google Scholar 

  13. Flintoff, W. E., Davidson, S. V., Siminovitch, L.: Isolation and partial characterization of three methotrexate-resistant phenotypes from Chinese hamster ovary cells. Somat. Cell Gent.2, 245–261 (1976).

    Google Scholar 

  14. Geissler, E., Scherneck, S., Waehlte, H., Zimmermann, W., Luebbe, L., Krause, H., Theile, M., Herold, H.-J., Rudolph, M., Weickmann, F., Nisch, G.: Further studies on the relation of SV 40 like viruses to human tumors. 7th Cold Spring Harbor Conference on Cell Proliferation: Viruses in naturally occurring tumors (in press, 1980).

  15. Graham, F. L., van der Eb, A. J.: A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology52, 456–467 (1973).

    Google Scholar 

  16. Graham, F. L., Abrahams, P. J., Mulder, C., Heijnecker, H. L., Warnaar, S. O., de Vries, F. A. J., Fiers, W., van der Eb, A. J.: Studies onin vitro transformation by DNA fragments of human adenovirus and Simian virus 40. Cold Spring Harbor Symp. Quant. Biol.39, 637–650 (1974).

    Google Scholar 

  17. Gupta, R. S., Flintoff, W. F., Siminovitch, L.: Purification and properties of dihydrofolate reductase from methotrexate-sensitive and methotrexate-resistant Chinese hamster ovary cells. Canad. J. Biochem.55, 445–452 (1977).

    Google Scholar 

  18. Harnden, D. G.: Viruses, chromosomes and tumors: The interaction between viruses and chromosomes. In:German, J. (ed.), Chromosomes and Cancer, 151 to 190. New York: J. Wiley and Sons 1974.

    Google Scholar 

  19. Hidaka, K., Endo, H., Akiyama, S.-J., Kuwano, M.: Isolation and characterization of amphotericin B-resistant cell lines in Chinese hamster cells. Cell14, 415 to 421 (1978).

    Google Scholar 

  20. Hirai, K., Defendi, V., Diamond, L.: Enhancement of Simian virus 40 transformation and integration by 4-nitroquinoline 1-oxide. Cancer Res.34, 3497–3500 (1974).

    Google Scholar 

  21. Hirai, K., Campbell, G., Defendi, V.: Changes of regulation of host DNA synthesis and viral DNA integration in SV 40-infected cells. In: Control of proliferation in animal cells. Cold Spring Harb. Symp. on Control of Proliferation of Animal Cells (1974), 151–166. Cold Spring Harbor: 1974.

  22. Hirt, B.: Selective extraction of polyoma DNA from infected mouse cell culture. J. mol. Biol.26, 365–369 (1967).

    Google Scholar 

  23. Horan, P. K., Jett, J. H., Romero, A., Lehman, J. M.: Flow microfluorometry analysis of DNA content in Chinese hamster cells following infection with Simian virus 40. Int. J. Cancer14, 514–521 (1974).

    Google Scholar 

  24. Howard, B. V., Estes, M. K., Pagano, J. S.: The uptake of SV 40 DNA by nonpermissive cells in the presence of DEAE-dextran. Biochim. biophys. Acta.228, 105–116 (1971).

    Google Scholar 

  25. Ide, T., Anzai, K., Andoh, T.: Enhancement of SV 40 transformation by treatment of C3H2K cells with UV light and caffeine. II. The effects of multiplicity of infection, cell phase and time with caffeine. Virology72, 480–485 (1976).

    Google Scholar 

  26. Kumar, B. V., Medoff, G., Kobayashi, G., Schlesinger, D.: Uptake ofEscherichia coli DNA into HeLa cells enhanced by amphotericin B. Nature250, 323–325 (1974).

    Google Scholar 

  27. Lago, C., Sartorius, B., Tramontano, D., Amati, P.: A cell membrane alteration specifically induced by SV 40 transformation. J. Cell Physiol.92, 265–274 (1977).

    Google Scholar 

  28. Lavialle, Ch., Stévenet, J., Morris, A. G., Suarez, H. G., Estrade, S., Salomon, J.-C., Cassingena, R.: Simian virus 40-Chinese hamster kidney cell interaction: I. Relationship of chromosome changes to transformation. Arch. Virol.49, 127–139 (1975).

    Google Scholar 

  29. Lehman, J. M., Bloustein, P.: Chromosome analysis and agglutination by concanavalin A of primary Simian virus 40-induced tumors. Int. J. Cancer14, 771–778 (1974).

    Google Scholar 

  30. Lehman, J. M.: Early chromosome changes in diploid Chinese hamster cells after infection with Simian virus 40. Int. J. Cancer13, 164–172 (1974).

    Google Scholar 

  31. Littlefield, J. W.: Hybridization of hamster cells with high and low folate reductase activity. Proc. Nat. Acad. Sci. (Wash.)62, 88–95 (1969).

    Google Scholar 

  32. Luebbe, L., Strauss, M., Geissler, E.: Reversion of HGPRT deficiency of skin fibroblasts from Lesch-Nyhan patients. In: Molecular Diseases (12th FEBS Meeting, Vol. 56, Dresden 1978), 67–78. Oxford-New York: Pergamon Press 1979.

    Google Scholar 

  33. Marshak, M. I., Varshaver, N. B., Shapiro, N. I.: Induction of gene mutations in cultured mammalian cells by the Simian virus 40. Genetika (U.S.S.R.)9, 138 141 (1973).

    Google Scholar 

  34. Martin, R. G., Persico-DiLauro, M., Edwards, C. A. F., Oppenheim, A.: The molecular basis of transformation by Simian virus 40. In: Genetic manipulation as it affects the cancer problem (Miami Winter-Symposia, Vol. 14), 87–102. New York: Academic Press 1977.

    Google Scholar 

  35. Milo, G. E., Blakeslee, J. R., Hart, R., John, D. S.: Chemical carcinogen alteration of SV 40 virus induced transformation of normal human cell populationsin vitro. Chem.-Biol. Interactions22, 185–197 (1978).

    Google Scholar 

  36. Myhr, B. C., DiPaolo, J. A.: Requirement for cell dispersion prior to selection of induced azaguanine-resistant colonies of Chinese hamster cells. Genetics80, 157–169 (1975).

    Google Scholar 

  37. Nichols, W. W., Bradt, C. I., Toji, L. H., Godley, M., Segawa, M.: Induction of sister chromatid exchanges by transformation with Simian virus 40. Cancer Res.38, 960–964 (1978).

    Google Scholar 

  38. Oudet, P., Gross-Belard, M., Chambon, P.: Electron microscopic and biochemical evidence that chromatin structure is a replicating unit. Cell4, 281–300 (1975).

    Google Scholar 

  39. Pagano, J. S.: Biological activity of isolated viral nucleic acids. Progr. med. Virol.12, 1–48 (1970).

    Google Scholar 

  40. Paucha, E., Mellor, A., Harvey, R., Smith, A. E., Hewick, R. M., Waterfield, M. D.: Large and small tumor antigens from SV 40 have identical amino termini mapping at 0.65 map units. Proc. Nat. Acad. Sci. (Wash.)75, 2165–2169 (1978).

    Google Scholar 

  41. Rigby, P.: The transforming genes of SV 40 and polyoma. Nature282, 781–784 (1979).

    Google Scholar 

  42. Sambrook, J.: The molecular biology of the papovaviruses. In:Nayak, D. P. (ed.), The molecular biology of animal viruses, Vol. 2, 589–672. New York-Basel: M. Dekker Inc. 1978.

    Google Scholar 

  43. Scherneck, S., Luebbe, L., Geissler, E., Nisch, G., Rudolph, M., Waehlte, H., Weickmann, F., Zimmermann, W.: Detection of Simian virus 40 related T-antigen in human meningiomas. Zbl. Neurochir.40, 121–130 (1979).

    Google Scholar 

  44. Scherneck, S., Rudolph, M., Geissler, E., Vogel, F., Luebbe, L., Waehlte, H., Nisch, G., Weickmann, F., Zimmermann, W.: Isolation of a SV 40-like papovavirus from a human glioblastoma. Int. J. Cancer24, 523–531 (1979).

    Google Scholar 

  45. Strauss, M., Theile, M., Eckert, R., Geissler, E.: Detection of antigenically active mutant HGPRT after mutagenesis with Simian virus 40. Mutation Res.51, 297–300 (1978).

    Google Scholar 

  46. Strauss, M., Theile, M., Geissler, E.: The incorporation of homologous and heterologous hypoxanthine-guanine phosphoribosyltransferase into mutant cells. Biochim. biophys. Acta.410, 426–430 (1978).

    Google Scholar 

  47. Theile, M., Scherneck, S., Geissler, E.: Mutagenesis by Simian virus 40. I. Detection of mutations in Chinese hamster cell lines using different resistance markers. Mutation Res.37, 111–124 (1976).

    Google Scholar 

  48. Theile, M., Strauss, M.: Mutagenesis by Simian virus 40. II. Changes in substrate affinities in mutant hypoxanthine-guanine phosphoribosyltransferase enzymes at different pH values. Mutation Res.45, 111–123 (1977).

    Google Scholar 

  49. Theile, M., Scherneck, S., Geissler, E.: Mutagenesis by Simian virus 40. IV. Influence of multiplicity of infection on the frequency of detectable resistance mutants in mammalian cells cultivatedin vitro. (In German.) Ergebn. exp. Med.34, 55–62 (1979).

    Google Scholar 

  50. Theile, M., Krause, H.: The combined mutagenic action of Simian virus 40 and other carcinogens in Chinese hamster cells. Stud. biophys.76, 45–46 (1979).

    Google Scholar 

  51. Theile, M., Strauss, M., Luebbe, L., Scherneck, S., Krause, H., Geissler, E.: SV 40-induced somatic mutations: Possible relevance to viral transformation. Cold Spring Harb. Symp. Quant. Biol.44, 377–382 (1980).

    Google Scholar 

  52. Varshaver, N. B., Marshak, M. I., Luss, E. V., Gorbunova, L. V., Shapiro, N. I.: Spontaneous, chemical and viral mutagenesis in temperature-sensitive glutamine-requiring Chinese hamster cells. Mutation Res.43, 263–278 (1977).

    Google Scholar 

  53. Waehlte, H., Scherneck, S.:In vitro transformation of primary Chinese hamster cells by minichromosomes from Simian virus 40. Arch. Geschwulstforsch.49, 475–484 (1979).

    Google Scholar 

  54. Weiner, L. P., Herndon, R. M., Narayan, O., Johnson, R. T., Shah, K., Rubinstein, L. J., Preziosi, T. J., Conley, F. K.: Isolation of virus related to SV 40 from patients with progressive multifocal leucoencephalopathy. N. Engl. J. Med.286, 385–390 (1972).

    Google Scholar 

  55. Weiss, A. F., Portmann, R., Fischer, H., Simon, J., Zang, K. D.: Simian virus 40-related antigens in three human meningiomas with defined chromosome loss. Proc. Nat. Acad. Sci. (Wash.)72, 609–613 (1975).

    Google Scholar 

  56. Zuna, R. E., Lehman, J. M.: Heterogeneity of karyotype and growth potential in Simian virus 40-transformed Chinese hamster cell clones. J. Nat. Cancer Inst.58, 1463–1472 (1977).

    Google Scholar 

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Theile, M., Scherneck, S. & Geissler, E. DNA of simian virus 40 mutates Chinese hamster cells. Archives of Virology 65, 293–309 (1980). https://doi.org/10.1007/BF01314545

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