Abstract
Hemizygous gyro male (Gy/Y) mice are a model for X-linked hypophosphataemic rickets. As in humans, the disease is caused by deletions in the Phex gene, a phosphate-regulating gene having homologies with endopeptidases on the X chromosome. Some phenotypic abnormalities in Gy/Y mice have recently been attributed to the fact that the Gy deletion also includes the neighbouring spermine synthase gene, resulting in spermine deficiency. Spermine and its precursors spermidine and putrescine are essential for cell growth and differentiation. As a novel method for studying the function of spermine, we established primary cultures of skin fibroblasts from hemizygous Gy/Y mice. The Gy/Y cells contained no detectable spermine. In view of the fact that spermine is a free-radical scavenger in vitro, we were surprised to find that Gy/Y cells were more resistant to oxidative stress than their normal (X/Y) counterparts. However, our finding that spermidine accumulates markedly in the spermine-deficient Gy/Y cells can probably explain this increased resistance. It is the first indication that spermidine can serve as a free-radical scavenger in vivo and not only in vitro. When subjecting the Gy/Y cells to UV-C irradiation we made another interesting finding: the mutant cells were more sensitive than the normal X/Y cells. This finding indicates that spermine, probably because of its high-affinity binding to DNA, is important in protection against chromatin damage.
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- Amores-Sánchez M. I., Medina M. A. Glutamine, as a precursor of glutathione, and oxidative stress. Mol Genet Metab. 1999 Jun;67(2):100–105. doi: 10.1006/mgme.1999.2857. [DOI] [PubMed] [Google Scholar]
- Auvinen M., Paasinen A., Andersson L. C., Hölttä E. Ornithine decarboxylase activity is critical for cell transformation. Nature. 1992 Nov 26;360(6402):355–358. doi: 10.1038/360355a0. [DOI] [PubMed] [Google Scholar]
- Beck L., Soumounou Y., Martel J., Krishnamurthy G., Gauthier C., Goodyer C. G., Tenenhouse H. S. Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice. J Clin Invest. 1997 Mar 15;99(6):1200–1209. doi: 10.1172/JCI119276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casero R. A., Jr, Mank A. R., Xiao L., Smith J., Bergeron R. J., Celano P. Steady-state messenger RNA and activity correlates with sensitivity to N1,N12-bis(ethyl)spermine in human cell lines representing the major forms of lung cancer. Cancer Res. 1992 Oct 1;52(19):5359–5363. [PubMed] [Google Scholar]
- Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
- Cozzi R., Perticone P., Bona R., Polani S. Antimutagenic activities of naturally occurring polyamines in Chinese hamster ovary cells in vitro. Environ Mol Mutagen. 1991;18(3):207–211. doi: 10.1002/em.2850180308. [DOI] [PubMed] [Google Scholar]
- Della Ragione F., Pegg A. E. Spermidine N-acetyltransferase. Methods Enzymol. 1983;94:321–325. doi: 10.1016/s0076-6879(83)94057-0. [DOI] [PubMed] [Google Scholar]
- Devitt G. P., Creagh E. M., Cotter T. G. The antioxidant 4b,5,9b,10-Tetrahydroindeno[1,2-b]indole inhibits apoptosis by preventing caspase activation following mitochondrial depolarization. Biochem Biophys Res Commun. 1999 Nov 2;264(3):622–629. doi: 10.1006/bbrc.1999.1576. [DOI] [PubMed] [Google Scholar]
- Eicher E. M., Southard J. L., Scriver C. R., Glorieux F. H. Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4667–4671. doi: 10.1073/pnas.73.12.4667. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Erwin B. G., Pegg A. E. Regulation of spermidine/spermine N1-acetyltransferase in L6 cells by polyamines and related compounds. Biochem J. 1986 Sep 1;238(2):581–587. doi: 10.1042/bj2380581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fozard J. R., Part M. L., Prakash N. J., Grove J., Schechter P. J., Sjoerdsma A., Koch-Weser J. L-Ornithine decarboxylase:an essential role in early mammalian embryogenesis. Science. 1980 May 2;208(4443):505–508. doi: 10.1126/science.6768132. [DOI] [PubMed] [Google Scholar]
- Friedman J., Cerutti P. The induction of ornithine decarboxylase by phorbol 12-myristate 13-acetate or by serum is inhibited by antioxidants. Carcinogenesis. 1983 Nov;4(11):1425–1427. doi: 10.1093/carcin/4.11.1425. [DOI] [PubMed] [Google Scholar]
- Grieff M., Whyte M. P., Thakker R. V., Mazzarella R. Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX. Genomics. 1997 Sep 1;44(2):227–231. doi: 10.1006/geno.1997.4876. [DOI] [PubMed] [Google Scholar]
- Ha H. C., Sirisoma N. S., Kuppusamy P., Zweier J. L., Woster P. M., Casero R. A., Jr The natural polyamine spermine functions directly as a free radical scavenger. Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11140–11145. doi: 10.1073/pnas.95.19.11140. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ha H. C., Yager J. D., Woster P. A., Casero R. A., Jr Structural specificity of polyamines and polyamine analogues in the protection of DNA from strand breaks induced by reactive oxygen species. Biochem Biophys Res Commun. 1998 Mar 6;244(1):298–303. doi: 10.1006/bbrc.1998.8258. [DOI] [PubMed] [Google Scholar]
- Harari P. M., Tome M. E., Fuller D. J., Carper S. W., Gerner E. W. Effects of diethyldithiocarbamate and endogenous polyamine content on cellular responses to hydrogen peroxide cytotoxicity. Biochem J. 1989 Jun 1;260(2):487–490. doi: 10.1042/bj2600487. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heby O., Persson L. Molecular genetics of polyamine synthesis in eukaryotic cells. Trends Biochem Sci. 1990 Apr;15(4):153–158. doi: 10.1016/0968-0004(90)90216-x. [DOI] [PubMed] [Google Scholar]
- Heller J. S., Fong W. F., Canellakis E. S. Induction of a protein inhibitor to ornithine decarboxylase by the end products of its reaction. Proc Natl Acad Sci U S A. 1976 Jun;73(6):1858–1862. doi: 10.1073/pnas.73.6.1858. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Iordanov M. S., Magun B. E. Different mechanisms of c-Jun NH(2)-terminal kinase-1 (JNK1) activation by ultraviolet-B radiation and by oxidative stressors. J Biol Chem. 1999 Sep 3;274(36):25801–25806. doi: 10.1074/jbc.274.36.25801. [DOI] [PubMed] [Google Scholar]
- Iordanov M. S., Pribnow D., Magun J. L., Dinh T. H., Pearson J. A., Magun B. E. Ultraviolet radiation triggers the ribotoxic stress response in mammalian cells. J Biol Chem. 1998 Jun 19;273(25):15794–15803. doi: 10.1074/jbc.273.25.15794. [DOI] [PubMed] [Google Scholar]
- Jansen C., Mattox D. E., Miller K. D., Brownell W. E. An animal model of hearing loss from alpha-difluoromethylornithine. Arch Otolaryngol Head Neck Surg. 1989 Oct;115(10):1234–1237. doi: 10.1001/archotol.1989.01860340088024. [DOI] [PubMed] [Google Scholar]
- Jänne J., Williams-Ashman H. G. On the purification of L-ornithine decarboxylase from rat prostate and effects of thiol compounds on the enzyme. J Biol Chem. 1971 Mar 25;246(6):1725–1732. [PubMed] [Google Scholar]
- KAISER D., TABOR H., TABOR C. W. Spermine protection of coliphage lambda DNA against breakage by hydrodynamic shear. J Mol Biol. 1963 Feb;6:141–147. doi: 10.1016/s0022-2836(63)80130-8. [DOI] [PubMed] [Google Scholar]
- Khan A. U., Di Mascio P., Medeiros M. H., Wilson T. Spermine and spermidine protection of plasmid DNA against single-strand breaks induced by singlet oxygen. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11428–11430. doi: 10.1073/pnas.89.23.11428. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Khan A. U., Mei Y. H., Wilson T. A proposed function for spermine and spermidine: protection of replicating DNA against damage by singlet oxygen. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11426–11427. doi: 10.1073/pnas.89.23.11426. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lorenz B., Francis F., Gempel K., Böddrich A., Josten M., Schmahl W., Schmidt J., Lehrach H., Meitinger T., Strom T. M. Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene. Hum Mol Genet. 1998 Mar;7(3):541–547. doi: 10.1093/hmg/7.3.541. [DOI] [PubMed] [Google Scholar]
- Lyon M. F., Scriver C. R., Baker L. R., Tenenhouse H. S., Kronick J., Mandla S. The Gy mutation: another cause of X-linked hypophosphatemia in mouse. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4899–4903. doi: 10.1073/pnas.83.13.4899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Løvaas E. Antioxidative and metal-chelating effects of polyamines. Adv Pharmacol. 1997;38:119–149. doi: 10.1016/s1054-3589(08)60982-5. [DOI] [PubMed] [Google Scholar]
- Matsufuji S., Matsufuji T., Miyazaki Y., Murakami Y., Atkins J. F., Gesteland R. F., Hayashi S. Autoregulatory frameshifting in decoding mammalian ornithine decarboxylase antizyme. Cell. 1995 Jan 13;80(1):51–60. doi: 10.1016/0092-8674(95)90450-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meyer R. A., Jr, Henley C. M., Meyer M. H., Morgan P. L., McDonald A. G., Mills C., Price D. K. Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse. Genomics. 1998 Mar 15;48(3):289–295. doi: 10.1006/geno.1997.5169. [DOI] [PubMed] [Google Scholar]
- Mizuno N., Kono T., Taniguchi S., Fukuda M., Maekawa N., Hisa T., Otani S., Hamada T. Effects of ultraviolet-B and PUVA on ornithine decarboxylase activity, DNA synthesis, and protein kinase C activity in mouse skin. J Dermatol. 1993 Feb;20(2):74–78. doi: 10.1111/j.1346-8138.1993.tb03834.x. [DOI] [PubMed] [Google Scholar]
- Murakami Y., Matsufuji S., Kameji T., Hayashi S., Igarashi K., Tamura T., Tanaka K., Ichihara A. Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination. Nature. 1992 Dec 10;360(6404):597–599. doi: 10.1038/360597a0. [DOI] [PubMed] [Google Scholar]
- Nilsson J., Koskiniemi S., Persson K., Grahn B., Holm I. Polyamines regulate both transcription and translation of the gene encoding ornithine decarboxylase antizyme in mouse. Eur J Biochem. 1997 Dec 1;250(2):223–231. doi: 10.1111/j.1432-1033.1997.0223a.x. [DOI] [PubMed] [Google Scholar]
- Oredsson S. M., Billgren M., Heby O. Induction of F9 embryonal carcinoma cell differentiation by inhibition of polyamine synthesis. Eur J Cell Biol. 1985 Sep;38(2):335–343. [PubMed] [Google Scholar]
- 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]
- Persson L., Holm I., Heby O. Regulation of ornithine decarboxylase mRNA translation by polyamines. Studies using a cell-free system and a cell line with an amplified ornithine decarboxylase gene. J Biol Chem. 1988 Mar 5;263(7):3528–3533. [PubMed] [Google Scholar]
- Pollard K. J., Samuels M. L., Crowley K. A., Hansen J. C., Peterson C. L. Functional interaction between GCN5 and polyamines: a new role for core histone acetylation. EMBO J. 1999 Oct 15;18(20):5622–5633. doi: 10.1093/emboj/18.20.5622. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seiler N., Knödgen B. High-performance liquid chromatographic procedure for the simultaneous determination of the natural polyamines and their monoacetyl derivatives. J Chromatogr. 1980 Dec 12;221(2):227–235. doi: 10.1016/s0378-4347(00)84307-8. [DOI] [PubMed] [Google Scholar]
- Shantz L. M., Pegg A. E. Overproduction of ornithine decarboxylase caused by relief of translational repression is associated with neoplastic transformation. Cancer Res. 1994 May 1;54(9):2313–2316. [PubMed] [Google Scholar]
- Snyder R. D. Inhibition of X-ray-induced DNA strand break repair in polyamine-depleted HeLa cells. Int J Radiat Biol. 1989 May;55(5):773–782. doi: 10.1080/09553008914550821. [DOI] [PubMed] [Google Scholar]
- Snyder R. D., Schroeder K. K. Radiosensitivity of polyamine-depleted HeLa cells and modulation by the aminothiol WR-1065. Radiat Res. 1994 Jan;137(1):67–75. [PubMed] [Google Scholar]
- Snyder R. D., Sunkara P. S. Effect of polyamine depletion on DNA damage and repair following UV irradiation of HeLa cells. Photochem Photobiol. 1990 Sep;52(3):525–532. doi: 10.1111/j.1751-1097.1990.tb01795.x. [DOI] [PubMed] [Google Scholar]
- Soriani M., Luscher P., Tyrrell R. M. Direct and indirect modulation of ornithine decarboxylase and cyclooxygenase by UVB radiation in human skin cells. Carcinogenesis. 1999 Apr;20(4):727–732. doi: 10.1093/carcin/20.4.727. [DOI] [PubMed] [Google Scholar]
- Splinter T. A., Romijn J. C. Phase I study of alpha-difluoromethylornithine and methyl-GAG. Eur J Cancer Clin Oncol. 1986 Jan;22(1):61–67. doi: 10.1016/0277-5379(86)90343-3. [DOI] [PubMed] [Google Scholar]
- Strom T. M., Francis F., Lorenz B., Böddrich A., Econs M. J., Lehrach H., Meitinger T. Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia. Hum Mol Genet. 1997 Feb;6(2):165–171. doi: 10.1093/hmg/6.2.165. [DOI] [PubMed] [Google Scholar]
- TABOR H. The protective effect of spermine and other polyamines against heat denaturation of deoxyribonucleic acid. Biochemistry. 1962 May 25;1:496–501. doi: 10.1021/bi00909a021. [DOI] [PubMed] [Google Scholar]
- Terleth C., van Laar T., Schouten R., van Steeg H., Hodemaekers H., Wormhoudt T., Cornelissen-Steijger P. D., Abrahams P. J., van der Eb A. J. A lack of radiation-induced ornithine decarboxylase activity prevents enhanced reactivation of herpes simplex virus and is linked to non-cancer proneness in xeroderma pigmentosum patients. Cancer Res. 1997 Oct 1;57(19):4384–4392. [PubMed] [Google Scholar]
- Thornalley P. J., Vasák M. Possible role for metallothionein in protection against radiation-induced oxidative stress. Kinetics and mechanism of its reaction with superoxide and hydroxyl radicals. Biochim Biophys Acta. 1985 Jan 21;827(1):36–44. doi: 10.1016/0167-4838(85)90098-6. [DOI] [PubMed] [Google Scholar]
- Tyrrell R. M. UV activation of mammalian stress proteins. EXS. 1996;77:255–271. [PubMed] [Google Scholar]
- Verma A. K., Lowe N. J., Boutwell R. K. Induction of mouse epidermal ornithine decarboxylase activity and DNA synthesis by ultraviolet light. Cancer Res. 1979 Mar;39(3):1035–1040. [PubMed] [Google Scholar]
- Widmann C., Gibson S., Johnson G. L. Caspase-dependent cleavage of signaling proteins during apoptosis. A turn-off mechanism for anti-apoptotic signals. J Biol Chem. 1998 Mar 20;273(12):7141–7147. doi: 10.1074/jbc.273.12.7141. [DOI] [PubMed] [Google Scholar]
- Williams K. Interactions of polyamines with ion channels. Biochem J. 1997 Jul 15;325(Pt 2):289–297. doi: 10.1042/bj3250289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Buul P. P., Tuinenburg-Bolraap A., Searle A. G., Natarajan A. T. A search for radiosensitive mouse mutants by use of the micronucleus technique. Mutat Res. 1987 Jul-Aug;191(3-4):163–169. doi: 10.1016/0165-7992(87)90148-5. [DOI] [PubMed] [Google Scholar]