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. 1989 Nov 1;263(3):745–752. doi: 10.1042/bj2630745

Expression of a human gene for polyamine transport in Chinese-hamster ovary cells.

T L Byers 1, R Wechter 1, M E Nuttall 1, A E Pegg 1
PMCID: PMC1133495  PMID: 2512913

Abstract

A molecular-genetic approach towards isolating mammalian polyamine-transport genes and their encoded proteins was devised involving the production of Chinese-hamster ovary (CHO) cells expressing a human polyamine-transport protein. CHO cells and a polyamine-transport-deficient CHO mutant cell line (CHOMG) were equally sensitive to the antiproliferative effects of alpha-difluoromethylornithine (DFMO), which blocked endogenous polyamine synthesis. Exposure to exogenous polyamines increased intracellular polyamine levels and reversed this DFMO-induced cytostasis in the CHO cells, but not in the CHOMG cells. CHOMG cells were therefore transfected with human DNA (isolated from HT-29 colon carcinoma cells) and cells expressing the human polyamine-transport system were identified by the ability of these cells to grow in a medium containing DFMO and polyamines. A number of different positive clones were identified and shown to have the capacity for polyamine uptake and an increased sensitivity to the toxic effects of the polyamine analogue methylglyoxal bis(guanylhydrazone). Differences in these properties between the clones are consistent with a multiplicity of polyamine-transport systems. Some clones also showed a change in growth characteristics, which may indicate a relationship between genes involved in the polyamine-transport system and in cell proliferation.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alhonen-Hongisto L., Seppänen P., Jänne J. Intracellular putrescine and spermidine deprivation induces increased uptake of the natural polyamines and methylglyoxal bis(guanylhydrazone). Biochem J. 1980 Dec 15;192(3):941–945. doi: 10.1042/bj1920941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  3. Byers T. L., Kameji R., Rannels D. E., Pegg A. E. Multiple pathways for uptake of paraquat, methylglyoxal bis(guanylhydrazone), and polyamines. Am J Physiol. 1987 Jun;252(6 Pt 1):C663–C669. doi: 10.1152/ajpcell.1987.252.6.C663. [DOI] [PubMed] [Google Scholar]
  4. Chang B. K., Libby P. R., Bergeron R. J., Porter C. W. Modulation of polyamine biosynthesis and transport by oncogene transfection. Biochem Biophys Res Commun. 1988 Nov 30;157(1):264–270. doi: 10.1016/s0006-291x(88)80042-1. [DOI] [PubMed] [Google Scholar]
  5. DisPasquale A., White D., McGuire J. Epidermal growth factor stimulates putrescine transport and ornithine decarboxylase activity in cultivated human fibroblasts. Exp Cell Res. 1978 Oct 15;116(2):317–323. doi: 10.1016/0014-4827(78)90454-8. [DOI] [PubMed] [Google Scholar]
  6. Feige J. J., Chambaz E. M. Polyamine uptake by bovine adrenocortical cells. Biochim Biophys Acta. 1985 Jul 30;846(1):93–100. doi: 10.1016/0167-4889(85)90114-4. [DOI] [PubMed] [Google Scholar]
  7. Feige J. J., Madani C., Chambaz E. M. Hormonal control of polyamine levels in bovine adrenocortical cells. Endocrinology. 1986 Mar;118(3):1059–1066. doi: 10.1210/endo-118-3-1059. [DOI] [PubMed] [Google Scholar]
  8. Gawel-Thompson K., Greene R. M. Characterization of a polyamine transport system in murine embryonic palate mesenchymal cells. J Cell Physiol. 1988 Aug;136(2):237–246. doi: 10.1002/jcp.1041360205. [DOI] [PubMed] [Google Scholar]
  9. Gordonsmith R. H., Smith L. L., Cohen G. M. Pulmonary accumulation of methylglyoxal-bis(guanylhydrazone) by the oligoamine uptake system. Biochem Pharmacol. 1985 May 15;34(10):1809–1816. doi: 10.1016/0006-2952(85)90653-7. [DOI] [PubMed] [Google Scholar]
  10. Heaton M. A., Flintoff W. F. Methylglyoxal-bis(guanylhydrazone)-resistant Chinese hamster ovary cells: genetic evidence that more than a single locus controls uptake. J Cell Physiol. 1988 Jul;136(1):133–139. doi: 10.1002/jcp.1041360117. [DOI] [PubMed] [Google Scholar]
  11. Heston W. D., Charles M. Calmodulin antagonist inhibition of polyamine transport in prostatic cancer cells in vitro. Biochem Pharmacol. 1988 Jul 1;37(13):2511–2514. doi: 10.1016/0006-2952(88)90239-0. [DOI] [PubMed] [Google Scholar]
  12. Jänne J., Hölttä E., Kallio A., Käpyaho K. Role of polyamines and their antimetabolites in clinical medicine. Spec Top Endocrinol Metab. 1983;5:227–293. [PubMed] [Google Scholar]
  13. Kakinuma Y., Hoshino K., Igarashi K. Characterization of the inducible polyamine transporter in bovine lymphocytes. Eur J Biochem. 1988 Sep 15;176(2):409–414. doi: 10.1111/j.1432-1033.1988.tb14297.x. [DOI] [PubMed] [Google Scholar]
  14. Kramer D. L., Paul B., Porter C. W. Effect of pretreatment with alpha-difluoromethylornithine on the selectivity of methylglyoxal bis(guanylhydrazone) for tumor tissue in L1210 leukemic mice. Cancer Res. 1985 Jun;45(6):2512–2515. [PubMed] [Google Scholar]
  15. Mandel J. L., Flintoff W. F. Isolation of mutant mammalian cells altered in polyamine transport. J Cell Physiol. 1978 Dec;97(3 Pt 1):335–343. doi: 10.1002/jcp.1040970308. [DOI] [PubMed] [Google Scholar]
  16. Pegg A. E., Borchardt R. T., Coward J. K. Effects of inhibitors of spermidine and spermine synthesis on polyamine concentrations and growth of transformed mouse fibroblasts. Biochem J. 1981 Jan 15;194(1):79–89. doi: 10.1042/bj1940079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pegg A. E., McCann P. P. Polyamine metabolism and function. Am J Physiol. 1982 Nov;243(5):C212–C221. doi: 10.1152/ajpcell.1982.243.5.C212. [DOI] [PubMed] [Google Scholar]
  18. Pegg A. E. Polyamine metabolism and its importance in neoplastic growth and a target for chemotherapy. Cancer Res. 1988 Feb 15;48(4):759–774. [PubMed] [Google Scholar]
  19. Pegg A. E. Recent advances in the biochemistry of polyamines in eukaryotes. Biochem J. 1986 Mar 1;234(2):249–262. doi: 10.1042/bj2340249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Persson L., Holm I., Ask A., Heby O. Curative effect of DL-2-difluoromethylornithine on mice bearing mutant L1210 leukemia cells deficient in polyamine uptake. Cancer Res. 1988 Sep 1;48(17):4807–4811. [PubMed] [Google Scholar]
  21. Pohjanpelto P. Putrescine transport is greatly increased in human fibroblasts initiated to proliferate. J Cell Biol. 1976 Mar;68(3):512–520. doi: 10.1083/jcb.68.3.512. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Porter C. W., Bergeron R. J. Enzyme regulation as an approach to interference with polyamine biosynthesis--an alternative to enzyme inhibition. Adv Enzyme Regul. 1988;27:57–79. doi: 10.1016/0065-2571(88)90009-x. [DOI] [PubMed] [Google Scholar]
  23. Porter C. W., McManis J., Casero R. A., Bergeron R. J. Relative abilities of bis(ethyl) derivatives of putrescine, spermidine, and spermine to regulate polyamine biosynthesis and inhibit L1210 leukemia cell growth. Cancer Res. 1987 Jun 1;47(11):2821–2825. [PubMed] [Google Scholar]
  24. Porter C. W., Miller J., Bergeron R. J. Aliphatic chain length specificity of the polyamine transport system in ascites L1210 leukemia cells. Cancer Res. 1984 Jan;44(1):126–128. [PubMed] [Google Scholar]
  25. Rinehart C. A., Jr, Chen K. Y. Characterization of the polyamine transport system in mouse neuroblastoma cells. Effects of sodium and system A amino acids. J Biol Chem. 1984 Apr 25;259(8):4750–4756. [PubMed] [Google Scholar]
  26. Rodrigues M. T., Palkonyay L., Sircar S., Fleurent J., Dessureault J., Weber J. M. Isolation and uptake characteristics of adenovirus transformed cell revertants resistant to the antiproliferative effects of methylglyoxal bis(guanylhydrazone). Biochem Biophys Res Commun. 1987 Sep 15;147(2):675–681. doi: 10.1016/0006-291x(87)90983-1. [DOI] [PubMed] [Google Scholar]
  27. Rubin J. S., Joyner A. L., Bernstein A., Whitmore G. F. Molecular identification of a human DNA repair gene following DNA-mediated gene transfer. Nature. 1983 Nov 10;306(5939):206–208. doi: 10.1038/306206a0. [DOI] [PubMed] [Google Scholar]
  28. Seppänen P., Alhonen-Hongisto L., Jänne J. Death of tumor cells in response to the use of a system of stimulated polyamine uptake from the transport of methylglyoxal bis(guanylhydrazone). Eur J Biochem. 1981 Sep 1;118(3):571–576. doi: 10.1111/j.1432-1033.1981.tb05557.x. [DOI] [PubMed] [Google Scholar]
  29. Sircar S., Palkonyay L., Rodrigues M., Allaire S., Horvath J., Thirion J. P., Weber J. Isolation of variants resistant to methylglyoxal bis(guanylhydrazone) from adenovirus-transformed rat cells. Cancer Res. 1987 Mar 1;47(5):1339–1343. [PubMed] [Google Scholar]
  30. Smith L. L., Wyatt I. The accumulation of putrescine into slices of rat lung and brain and its relationship to the accumulation of paraquat. Biochem Pharmacol. 1981 May 15;30(10):1053–1058. doi: 10.1016/0006-2952(81)90441-x. [DOI] [PubMed] [Google Scholar]
  31. Tabor C. W., Tabor H. Polyamines. Annu Rev Biochem. 1984;53:749–790. doi: 10.1146/annurev.bi.53.070184.003533. [DOI] [PubMed] [Google Scholar]
  32. Wallace H. M., Keir H. M. A comparison of polyamine metabolism in normal and transformed baby-hamster-kidney cells. Biochem J. 1982 Mar 15;202(3):785–790. doi: 10.1042/bj2020785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wigler M., Silverstein S., Lee L. S., Pellicer A., Cheng Y. c., Axel R. Transfer of purified herpes virus thymidine kinase gene to cultured mouse cells. Cell. 1977 May;11(1):223–232. doi: 10.1016/0092-8674(77)90333-6. [DOI] [PubMed] [Google Scholar]

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