Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1996 Jun 1;316(Pt 2):421–425. doi: 10.1042/bj3160421

Regulation of the salvage pathway of deoxynucleotides synthesis in apoptosis induced by growth factor deprivation.

F J Oliver 1, M K Collins 1, A López-Rivas 1
PMCID: PMC1217367  PMID: 8687383

Abstract

Here we describe changes in dNTP metabolism that precede DNA fragmentation in a model of apoptosis driven by deprivation of the cytokine interleukin 3 (IL-3). In haemopoietic BAF3 cells, IL-3 withdrawal leads to a rapid decrease in the size of dATP, dTTP and dGTP pools without affecting dCTP levels. This imbalance in dNTP pools precedes DNA fragmentation and is accompanied by down-regulation of enzymes controlling the de novo and salvage pathways of dNTP synthesis, ribonucleotide reductase and thymidine kinase (TK) respectively. Readdition of IL-3 results in a rapid, protein synthesis-independent restoration of normal dNTP pools, enhanced TK activity and increased precursor incorporation through the salvage pathway. Up-regulation of TK activity after IL-3 readdition is prevented by the protein kinase C (PKC) inhibitor staurosporin, but not by tyrosine kinase inhibitors. Furthermore activation of PKC by phorbol esters mimics the stimulatory effect of IL-3 on TK activity, suggesting that PKC might be involved in regulating this effect. These results indicate that regulation by IL-3 of the salvage pathway of dNTP synthesis plays a role in the maintenance of cellular dNTP pool balance and suggests that alterations in dNTP metabolism after IL-3 deprivation could be a relevant event in the commitment of haemopoietic cells to apoptosis.

Full Text

The Full Text of this article is available as a PDF (329.3 KB).

Selected References

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

  1. Abe K., Yoshida M., Usui T., Horinouchi S., Beppu T. Highly synchronous culture of fibroblasts from G2 block caused by staurosporine, a potent inhibitor of protein kinases. Exp Cell Res. 1991 Jan;192(1):122–127. doi: 10.1016/0014-4827(91)90166-r. [DOI] [PubMed] [Google Scholar]
  2. Almasan A., Yin Y., Kelly R. E., Lee E. Y., Bradley A., Li W., Bertino J. R., Wahl G. M. Deficiency of retinoblastoma protein leads to inappropriate S-phase entry, activation of E2F-responsive genes, and apoptosis. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5436–5440. doi: 10.1073/pnas.92.12.5436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Andrejauskas E., Moroni C. Reversible abrogation of IL-3 dependence by an inducible H-ras oncogene. EMBO J. 1989 Sep;8(9):2575–2581. doi: 10.1002/j.1460-2075.1989.tb08396.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ascaso R., Marvel J., Collins M. K., López-Rivas A. Interleukin-3 and Bcl-2 cooperatively inhibit etoposide-induced apoptosis in a murine pre-B cell line. Eur J Immunol. 1994 Mar;24(3):537–541. doi: 10.1002/eji.1830240307. [DOI] [PubMed] [Google Scholar]
  5. Bebenek K., Kunkel T. A. Frameshift errors initiated by nucleotide misincorporation. Proc Natl Acad Sci U S A. 1990 Jul;87(13):4946–4950. doi: 10.1073/pnas.87.13.4946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bianchi V., Pontis E., Reichard P. Changes of deoxyribonucleoside triphosphate pools induced by hydroxyurea and their relation to DNA synthesis. J Biol Chem. 1986 Dec 5;261(34):16037–16042. [PubMed] [Google Scholar]
  7. Bianchi V., Pontis E., Reichard P. Regulation of pyrimidine deoxyribonucleotide metabolism by substrate cycles in dCMP deaminase-deficient V79 hamster cells. Mol Cell Biol. 1987 Dec;7(12):4218–4224. doi: 10.1128/mcb.7.12.4218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chang Z. F., Cheng S. M. Constitutive overexpression of DNA binding activity to the distal CCAAT box of human thymidine kinase promoter in human tumor cell lines. Cancer Res. 1993 Jul 15;53(14):3253–3256. [PubMed] [Google Scholar]
  9. Chang Z. F., Huang D. Y., Hsue N. C. Differential phosphorylation of human thymidine kinase in proliferating and M phase-arrested human cells. J Biol Chem. 1994 Aug 19;269(33):21249–21254. [PubMed] [Google Scholar]
  10. Chang Z. F., Huang D. Y. The regulation of thymidine kinase in HL-60 human promyeloleukemia cells. J Biol Chem. 1993 Jan 15;268(2):1266–1271. [PubMed] [Google Scholar]
  11. Cheng Y. C. Thymidine kinase from blast cells of myelocytic leukemia. Methods Enzymol. 1978;51:365–371. doi: 10.1016/s0076-6879(78)51049-5. [DOI] [PubMed] [Google Scholar]
  12. Cohen J. J., Duke R. C., Fadok V. A., Sellins K. S. Apoptosis and programmed cell death in immunity. Annu Rev Immunol. 1992;10:267–293. doi: 10.1146/annurev.iy.10.040192.001411. [DOI] [PubMed] [Google Scholar]
  13. Collins M. K., Marvel J., Malde P., Lopez-Rivas A. Interleukin 3 protects murine bone marrow cells from apoptosis induced by DNA damaging agents. J Exp Med. 1992 Oct 1;176(4):1043–1051. doi: 10.1084/jem.176.4.1043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Cory J. G., Russell F. A., Mansell M. M. A convenient assay for ADP reductase activity using Dowex-1-borate columns. Anal Biochem. 1973 Oct;55(2):449–456. doi: 10.1016/0003-2697(73)90135-8. [DOI] [PubMed] [Google Scholar]
  15. Elledge S. J., Zhou Z., Allen J. B. Ribonucleotide reductase: regulation, regulation, regulation. Trends Biochem Sci. 1992 Mar;17(3):119–123. doi: 10.1016/0968-0004(92)90249-9. [DOI] [PubMed] [Google Scholar]
  16. Eriksson S., Arnér E., Spasokoukotskaja T., Wang L., Karlsson A., Brosjö O., Gunvén P., Julusson G., Liliemark J. Properties and levels of deoxynucleoside kinases in normal and tumor cells; implications for chemotherapy. Adv Enzyme Regul. 1994;34:13–25. doi: 10.1016/0065-2571(94)90006-x. [DOI] [PubMed] [Google Scholar]
  17. Ferraro P., Bianchi V., Biasin M. R., Celotti L. Deoxynucleotide pools and DNA synthesis in resting and PHA-stimulated human lymphocytes treated with mutagens. Exp Cell Res. 1992 Apr;199(2):349–354. doi: 10.1016/0014-4827(92)90444-d. [DOI] [PubMed] [Google Scholar]
  18. Gao W. Y., Cara A., Gallo R. C., Lori F. Low levels of deoxynucleotides in peripheral blood lymphocytes: a strategy to inhibit human immunodeficiency virus type 1 replication. Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):8925–8928. doi: 10.1073/pnas.90.19.8925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Greger J., Dramiński M. Growth inhibition of Kirkman-Robbins hepatoma by 1-(1,3-dihydroxy-2-propoxymethyl)-5,6-tetramethyleneuracil and possible mechanism of its biological activity. Z Naturforsch C. 1989 Nov-Dec;44(11-12):985–991. [PubMed] [Google Scholar]
  20. Höglund L., Pontis E., Reichard P. Effects of deoxycytidine and thymidine kinase deficiency on substrate cycles between deoxyribonucleosides and their 5'-phosphates. Cancer Res. 1988 Jul 1;48(13):3681–3687. [PubMed] [Google Scholar]
  21. Ihle J. N. Cytokine receptor signalling. Nature. 1995 Oct 19;377(6550):591–594. doi: 10.1038/377591a0. [DOI] [PubMed] [Google Scholar]
  22. Jacobson M. D., Burne J. F., Raff M. C. Programmed cell death and Bcl-2 protection in the absence of a nucleus. EMBO J. 1994 Apr 15;13(8):1899–1910. doi: 10.1002/j.1460-2075.1994.tb06459.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kinoshita T., Yokota T., Arai K., Miyajima A. Suppression of apoptotic death in hematopoietic cells by signalling through the IL-3/GM-CSF receptors. EMBO J. 1995 Jan 16;14(2):266–275. doi: 10.1002/j.1460-2075.1995.tb07000.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Kizaki H., Shimada H., Ohsaka F., Sakurada T. Adenosine, deoxyadenosine, and deoxyguanosine induce DNA cleavage in mouse thymocytes. J Immunol. 1988 Sep 1;141(5):1652–1657. [PubMed] [Google Scholar]
  25. Kwok J. B., Tattersall M. H. DNA fragmentation, dATP pool elevation and potentiation of antifolate cytotoxicity in L1210 cells by hypoxanthine. Br J Cancer. 1992 Apr;65(4):503–508. doi: 10.1038/bjc.1992.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lindberg U., Skoog L. A method for the determination of dATP and dTTP in picomole amounts. Anal Biochem. 1970 Mar;34:152–160. doi: 10.1016/0003-2697(70)90096-5. [DOI] [PubMed] [Google Scholar]
  27. Mathews C. K., Ji J. DNA precursor asymmetries, replication fidelity, and variable genome evolution. Bioessays. 1992 May;14(5):295–301. doi: 10.1002/bies.950140502. [DOI] [PubMed] [Google Scholar]
  28. Mattano S. S., Palella T. D., Mitchell B. S. Mutations induced at the hypoxanthine-guanine phosphoribosyltransferase locus of human T-lymphoblasts by perturbations of purine deoxyribonucleoside triphosphate pools. Cancer Res. 1990 Aug 1;50(15):4566–4571. [PubMed] [Google Scholar]
  29. Metcalf D. The molecular control of cell division, differentiation commitment and maturation in haemopoietic cells. Nature. 1989 May 4;339(6219):27–30. doi: 10.1038/339027a0. [DOI] [PubMed] [Google Scholar]
  30. Miyashita T., Reed J. C. bcl-2 gene transfer increases relative resistance of S49.1 and WEHI7.2 lymphoid cells to cell death and DNA fragmentation induced by glucocorticoids and multiple chemotherapeutic drugs. Cancer Res. 1992 Oct 1;52(19):5407–5411. [PubMed] [Google Scholar]
  31. North T. W., Bestwick R. K., Mathews C. K. Detection of activities that interfere with the enzymatic assay of deoxyribonucleoside 5'-triphosphates. J Biol Chem. 1980 Jul 25;255(14):6640–6645. [PubMed] [Google Scholar]
  32. Oliver F. J., Marvel J., Collins M. K., López-Rivas A. Bcl-2 oncogene protects a bone marrow-derived pre-B-cell line from 5'-fluor,2'-deoxyuridine-induced apoptosis. Biochem Biophys Res Commun. 1993 Jul 15;194(1):126–132. doi: 10.1006/bbrc.1993.1794. [DOI] [PubMed] [Google Scholar]
  33. Palacios R., Steinmetz M. Il-3-dependent mouse clones that express B-220 surface antigen, contain Ig genes in germ-line configuration, and generate B lymphocytes in vivo. Cell. 1985 Jul;41(3):727–734. doi: 10.1016/s0092-8674(85)80053-2. [DOI] [PubMed] [Google Scholar]
  34. Petersen L. N., Orren D. K., Bohr V. A. Gene-specific and strand-specific DNA repair in the G1 and G2 phases of the cell cycle. Mol Cell Biol. 1995 Jul;15(7):3731–3737. doi: 10.1128/mcb.15.7.3731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Rao P., Kitamura T., Miyajima A., Mufson R. A. Human IL-3 receptor signaling: rapid induction of phosphatidylcholine hydrolysis is independent of protein kinase C but dependent on tyrosine phosphorylation in transfected NIH 3T3 cells. J Immunol. 1995 Feb 15;154(4):1664–1674. [PubMed] [Google Scholar]
  36. Reichard P. Interactions between deoxyribonucleotide and DNA synthesis. Annu Rev Biochem. 1988;57:349–374. doi: 10.1146/annurev.bi.57.070188.002025. [DOI] [PubMed] [Google Scholar]
  37. Rodriguez-Tarduchy G., Collins M., López-Rivas A. Regulation of apoptosis in interleukin-3-dependent hemopoietic cells by interleukin-3 and calcium ionophores. EMBO J. 1990 Sep;9(9):2997–3002. doi: 10.1002/j.1460-2075.1990.tb07492.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sato N., Sakamaki K., Terada N., Arai K., Miyajima A. Signal transduction by the high-affinity GM-CSF receptor: two distinct cytoplasmic regions of the common beta subunit responsible for different signaling. EMBO J. 1993 Nov;12(11):4181–4189. doi: 10.1002/j.1460-2075.1993.tb06102.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Schrader J. W. The panspecific hemopoietin of activated T lymphocytes (interleukin-3). Annu Rev Immunol. 1986;4:205–230. doi: 10.1146/annurev.iy.04.040186.001225. [DOI] [PubMed] [Google Scholar]
  40. Whetton A. D., Monk P. N., Consalvey S. D., Huang S. J., Dexter T. M., Downes C. P. Interleukin 3 stimulates proliferation via protein kinase C activation without increasing inositol lipid turnover. Proc Natl Acad Sci U S A. 1988 May;85(10):3284–3288. doi: 10.1073/pnas.85.10.3284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Williams G. T., Smith C. A., Spooncer E., Dexter T. M., Taylor D. R. Haemopoietic colony stimulating factors promote cell survival by suppressing apoptosis. Nature. 1990 Jan 4;343(6253):76–79. doi: 10.1038/343076a0. [DOI] [PubMed] [Google Scholar]
  42. Wojcik B. E., Dermody J. J., Ozer H. L., Mun B., Mathews C. K. Temperature-sensitive DNA mutant of Chinese hamster ovary cells with a thermolabile ribonucleotide reductase activity. Mol Cell Biol. 1990 Nov;10(11):5688–5699. doi: 10.1128/mcb.10.11.5688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Yoshioka A., Tanaka S., Hiraoka O., Koyama Y., Hirota Y., Ayusawa D., Seno T., Garrett C., Wataya Y. Deoxyribonucleoside triphosphate imbalance. 5-Fluorodeoxyuridine-induced DNA double strand breaks in mouse FM3A cells and the mechanism of cell death. J Biol Chem. 1987 Jun 15;262(17):8235–8241. [PubMed] [Google Scholar]
  44. al-Nabulsi I., Takamiya Y., Voloshin Y., Dritschilo A., Martuza R. L., Jorgensen T. J. Expression of thymidine kinase is essential to low dose radiation resistance of rat glioma cells. Cancer Res. 1994 Nov 1;54(21):5614–5617. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES