Skip to main content
Log in

Genetic and biochemical studies with the adenosine analogs toyocamycin and tubercidin: Mutation at the adenosine kinase locus in Chinese hamster cells

  • Published:
Somatic Cell Genetics

Abstract

The pyrrolopyrimidine nucleosides toyocamycin and tubercidin show several unique features of growth inhibition in Chinese hamster ovary (CHO) cells. Stable mutants which are more than 500-fold resistant to these drugs are obtained in CHO cells at a strikingly high frequency of approximately 10−3,in the absence of mutagenesis. The mutants resistant to toyocamycin (Toy r)and tubercidin (Tub r)exhibit similar crossresistance patterns to the two selective drugs as well as to adenosine and 6-methyl mercaptopurine riboside, indicating that the same lesion is probably involved in all cases. The mutants examined were found to be deficient in the enzyme adenosine kinase (AK), indicating that the phosphorylation of these analogs is an essential first step in their toxic action. The above mutants (AK )behaved recessively in cell hybrids, and segregation studies indicate that the AK locus is not linked to the X chromosome. The frequencies of similar Toy r mutants in other Chinese hamster lines, e.g., V79, CHW, M3-1, GM7, and CHO-K1, varied from similar to more than three logs less than that observed for CHO cells, indicating that various cell lines probably differ in the number of functional gene copies for this locus.

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.

Institutional subscriptions

Similar content being viewed by others

Literature cited

  1. Acs, G., and Reich, E. (1967). InAntibiotics, Vol. 1 (eds.) Gottlieb, D., and Shaw, P. D. (Springer-Verlag, New York), pp. 494–498.

    Google Scholar 

  2. Suhadolnik, R. J. (1970). InNucleoside Antibiotics (Wiley-Interscience, New York), pp. 298–353.

    Google Scholar 

  3. Brdar, B., Rifkin, D. B., and Reich, E. (1973).J. Biol. Chem. 248:2397–2408.

    PubMed  Google Scholar 

  4. Bloch, A., Leonard, R. J., and Nichol, C. A. (1967).Biochim. Biophys. Acta 138:10–25.

    PubMed  Google Scholar 

  5. Ross, A. F., and Jaffe, J. A. (1972).Biochem. Pharmacol. 21:3059–3069.

    PubMed  Google Scholar 

  6. Jaffe, J. A. (1975).Ann. N. Y. Acad. Sci. 255:306–316.

    PubMed  Google Scholar 

  7. Sneft, A. W., and Crabtree, G. W. (1977).Biochem. Pharmacol. 26:1847–1855.

    PubMed  Google Scholar 

  8. Owen, S. P., and Smith, P. (1964).Cancer Chemother. Rep. 36:19–22.

    PubMed  Google Scholar 

  9. Klein, E., Burgess, G. H., Bloch, A., Milgrom, H., and Holtermann, O. A. (1975).Ann. N. Y. Acad. Sci. 255:216–224.

    PubMed  Google Scholar 

  10. Gupta, R. S., and Siminovitch, L. (1976).Cell 9:213–219.

    PubMed  Google Scholar 

  11. Gupta, R.S., and Siminovitch, L. (1978).Somat. Cell Genet. 4:77–94.

    PubMed  Google Scholar 

  12. Gupta, R. S., and Siminovitch, L. (1978).Somat. Cell Genet. 4:355–374.

    PubMed  Google Scholar 

  13. Gupta, R. S., and Siminovitch, L. (1978).Somat. Cell Genet. 4:553–571.

    PubMed  Google Scholar 

  14. Kao, F. T., and Puck, T. T. (1967).Genetics 55:513–524.

    PubMed  Google Scholar 

  15. Worton, R. G., Ho, C. C., and Duff, C. (1977).Somat. Cell Genet. 3:27–45.

    PubMed  Google Scholar 

  16. McBurney, M. W., and Whitmore, G. F. (1974).Cell 2:173–188.

    PubMed  Google Scholar 

  17. Chasin, L. A. (1972).Nature (London) New Biol. 240:50–52.

    Google Scholar 

  18. Gray, J. W., Carrano, A. V., Steinmetz, L. L., Van Dilla, M. A., Moore II, D. H., Mayall, B. H., and Mendelsohn, M. L. (1975).Proc. Natl. Acad. Sci. U.S.A. 72:1231–1234.

    PubMed  Google Scholar 

  19. Thirion, J. P., Banville, D., and Noel, H. (1976).Genetics 83:173–174.

    Google Scholar 

  20. Lin, C. C., Chang, T., and Niewczas-Late, V. (1971).Can. J. Genet. Cytol. 13:9–13.

    PubMed  Google Scholar 

  21. Stanners, C. P., Elicieri, G. L., and Green, H. (1971).Nature (London) New Biol. 230:52–54.

    Google Scholar 

  22. Norwood, T. H., Zeigler, C. J., and Martin, G. M. (1976).Somat. Cell Genet. 2:263–270.

    PubMed  Google Scholar 

  23. Chan, T., Ishii, K., Long, C., and Green, H. (1973).J. Cell Physiol. 81:315–322.

    PubMed  Google Scholar 

  24. Bakay, B., Telfer, M. A., and Nyhan, W. L. (1969).Biochem. Med. 3:230–243.

    Google Scholar 

  25. Lowry, O. H., Rosebrough, N. J., Farr, A. L., and Randall, R. J. (1951).J. Biol. Chem. 193:265–275.

    PubMed  Google Scholar 

  26. Acs, G., Reich, E., and Mori, M. (1964).Proc. Natl. Acad. Sci. U.S.A. 52:493–501.

    PubMed  Google Scholar 

  27. Tavitan, A., Uretsky, S. C., and Acs, G. (1968).Biochim. Biophys. Acta 157:33–42.

    PubMed  Google Scholar 

  28. Luria, S. E., and Delbruck, M. (1943).Genetics 28:491–511.

    Google Scholar 

  29. Capizzi, R. L., and Jameson, J. W. (1973).Mutat. Res. 17:147–148.

    PubMed  Google Scholar 

  30. Bennett, L. L., Jr., Schnebli, H. P., Vail, M. H., Allan, P. W., and Montgomery, J. A. (1966).Mol. Pharmacol. 2:432–443.

    PubMed  Google Scholar 

  31. McBurney, M. W., and Whitmore, G. F. (1974).J. Cell. Physiol. 85:87–100.

    Google Scholar 

  32. Debatisse, M., and Buttin, G. (1977).Somat. Cell Genet. 3:497–511.

    PubMed  Google Scholar 

  33. Chan, T., Creagan, R. P. and Reardon, M. P. (1978).Somat. Cell Genet. 4:1–12.

    PubMed  Google Scholar 

  34. Farrell, S. A., and Worton, R. G. (1977).Somat. Cell Genet. 3:539–551.

    PubMed  Google Scholar 

  35. Gupta, R. S., Chan, D. H. Y., and Siminovitch, L. (1978).Cell 15:1007–1013.

    Google Scholar 

  36. Campbell, C., and Worton, R. G. (1978).Cell (in press).

  37. Gupta, R. S., Chan, D. H. Y., and Siminovitch, L. (1978).J. Cell. Physiol. (in press).

  38. Siminovitch, L. (1976).Cell 7:1–11.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gupta, R.S., Siminovitch, L. Genetic and biochemical studies with the adenosine analogs toyocamycin and tubercidin: Mutation at the adenosine kinase locus in Chinese hamster cells. Somat Cell Mol Genet 4, 715–735 (1978). https://doi.org/10.1007/BF01543160

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01543160

Keywords

Navigation