Abstract
We studied the relative efficacy of polyamines to facilitate the binding of estrogen receptor to poly(dA-dC).poly(dG-dT). In the absence of polyamines, 1,400 micrograms/ml of this polynucleotide eluted 50% of bound estrogen receptor from DNA-cellulose. In contrast, 50% estrogen receptor was eluted by 65 micrograms/ml of poly(dA-dC).poly(dG-dT) complexed with 150 microM spermidine. Putrescine and spermine also enhanced the ability of poly(dA-dC).poly(dG-dT) to elute estrogen receptor, but the magnitude of the effect was not as high as that of spermidine. Control experiments with calf thymus DNA and poly(dA-dT).poly(dA-dT) showed 6- and 3-fold increase, respectively in their affinity for estrogen receptor in the presence of spermidine. The dramatic increase in the affinity of poly(dA-dC).poly(dG-dT) for estrogen receptor in the presence of polyamines might be a result of the conversion of the polynucleotide to the left-handed Z-DNA form. These results show that polyamines are capable of participating in estrogenic regulation of gene expression by altering the affinity of the receptor for specific DNA sequences.
Full text
PDF















Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ausio J., Zhou G., van Holde K. A reexamination of the reported B----Z DNA transition in nucleosomes reconstituted with poly(dG-m5dC).poly(dG-m5dC). Biochemistry. 1987 Sep 8;26(18):5595–5599. doi: 10.1021/bi00392a003. [DOI] [PubMed] [Google Scholar]
- BURTON K. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J. 1956 Feb;62(2):315–323. doi: 10.1042/bj0620315. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beato M. Induction of transcription by steroid hormones. Biochim Biophys Acta. 1987 Nov 20;910(2):95–102. doi: 10.1016/0167-4781(87)90060-1. [DOI] [PubMed] [Google Scholar]
- Dahmer M. K., Housley P. R., Pratt W. B. Effects of molybdate and endogenous inhibitors on steroid-receptor inactivation, transformation, and translocation. Annu Rev Physiol. 1984;46:67–81. doi: 10.1146/annurev.ph.46.030184.000435. [DOI] [PubMed] [Google Scholar]
- Feigon J., Wang A. H., van der Marel G. A., van Boom J. H., Rich A. Z-DNA forms without an alternating purine-pyrimidine sequence in solution. Science. 1985 Oct 4;230(4721):82–84. doi: 10.1126/science.4035359. [DOI] [PubMed] [Google Scholar]
- Gorski J., Gannon F. Current models of steroid hormone action: a critique. Annu Rev Physiol. 1976;38:425–450. doi: 10.1146/annurev.ph.38.030176.002233. [DOI] [PubMed] [Google Scholar]
- Grody W. W., Schrader W. T., O'Malley B. W. Activation, transformation, and subunit structure of steroid hormone receptors. Endocr Rev. 1982 Spring;3(2):141–163. doi: 10.1210/edrv-3-2-141. [DOI] [PubMed] [Google Scholar]
- Hamada H., Kakunaga T. Potential Z-DNA forming sequences are highly dispersed in the human genome. Nature. 1982 Jul 22;298(5872):396–398. doi: 10.1038/298396a0. [DOI] [PubMed] [Google Scholar]
- Haniford D. B., Pulleyblank D. E. Facile transition of poly[d(TG) x d(CA)] into a left-handed helix in physiological conditions. Nature. 1983 Apr 14;302(5909):632–634. doi: 10.1038/302632a0. [DOI] [PubMed] [Google Scholar]
- Hayes T. E., Dixon J. E. Z-DNA in the rat somatostatin gene. J Biol Chem. 1985 Jul 5;260(13):8145–8156. [PubMed] [Google Scholar]
- Jensen E. V., Suzuki T., Kawashima T., Stumpf W. E., Jungblut P. W., DeSombre E. R. A two-step mechanism for the interaction of estradiol with rat uterus. Proc Natl Acad Sci U S A. 1968 Feb;59(2):632–638. doi: 10.1073/pnas.59.2.632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jänne J., Pösö H., Raina A. Polyamines in rapid growth and cancer. Biochim Biophys Acta. 1978 Apr 6;473(3-4):241–293. doi: 10.1016/0304-419x(78)90015-x. [DOI] [PubMed] [Google Scholar]
- Kallos J., Hollander V. P. Assessment of specificity of oestrogen receptor-DNA interaction by a competitive assay. Nature. 1978 Mar 9;272(5649):177–179. doi: 10.1038/272177a0. [DOI] [PubMed] [Google Scholar]
- Kilpatrick M. W., Klysik J., Singleton C. K., Zarling D. A., Jovin T. M., Hanau L. H., Erlanger B. F., Wells R. D. Intervening sequences in human fetal globin genes adopt left-handed Z helices. J Biol Chem. 1984 Jun 10;259(11):7268–7274. [PubMed] [Google Scholar]
- King W. J., Greene G. L. Monoclonal antibodies localize oestrogen receptor in the nuclei of target cells. Nature. 1984 Feb 23;307(5953):745–747. doi: 10.1038/307745a0. [DOI] [PubMed] [Google Scholar]
- Knowler J. T., Beaumont J. M. The mechanism of action of oestrogens. Essays Biochem. 1985;20:1–39. [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Lafer E. M., Sousa R., Rich A. Anti-Z-DNA antibody binding can stabilize Z-DNA in relaxed and linear plasmids under physiological conditions. EMBO J. 1985 Dec 30;4(13B):3655–3660. doi: 10.1002/j.1460-2075.1985.tb04131.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lima G., Shiu R. P. Role of polyamines in estradiol-induced growth of human breast cancer cells. Cancer Res. 1985 Jun;45(6):2466–2470. [PubMed] [Google Scholar]
- Manni A., Wright C. Reversal of the antiproliferative effect of the antiestrogen tamoxifen by polyamines in breast cancer cells. Endocrinology. 1984 Mar;114(3):836–839. doi: 10.1210/endo-114-3-836. [DOI] [PubMed] [Google Scholar]
- Maurer R. A. Selective binding of the estradiol receptor to a region at least one kilobase upstream from the rat prolactin gene. DNA. 1985 Feb;4(1):1–9. doi: 10.1089/dna.1985.4.1. [DOI] [PubMed] [Google Scholar]
- Moreau P., Hen R., Wasylyk B., Everett R., Gaub M. P., Chambon P. The SV40 72 base repair repeat has a striking effect on gene expression both in SV40 and other chimeric recombinants. Nucleic Acids Res. 1981 Nov 25;9(22):6047–6068. doi: 10.1093/nar/9.22.6047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mulvihill E. R., LePennec J. P., Chambon P. Chicken oviduct progesterone receptor: location of specific regions of high-affinity binding in cloned DNA fragments of hormone-responsive genes. Cell. 1982 Mar;28(3):621–632. doi: 10.1016/0092-8674(82)90217-3. [DOI] [PubMed] [Google Scholar]
- Nordheim A., Rich A. Negatively supercoiled simian virus 40 DNA contains Z-DNA segments within transcriptional enhancer sequences. Nature. 1983 Jun 23;303(5919):674–679. doi: 10.1038/303674a0. [DOI] [PubMed] [Google Scholar]
- O'Malley B. W. Steroid hormone action in eucaryotic cells. J Clin Invest. 1984 Aug;74(2):307–312. doi: 10.1172/JCI111425. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Pfahl M. Specific binding of the glucocorticoid-receptor complex to the mouse mammary tumor proviral promoter region. Cell. 1982 Dec;31(2 Pt 1):475–482. doi: 10.1016/0092-8674(82)90140-4. [DOI] [PubMed] [Google Scholar]
- Rich A., Nordheim A., Wang A. H. The chemistry and biology of left-handed Z-DNA. Annu Rev Biochem. 1984;53:791–846. doi: 10.1146/annurev.bi.53.070184.004043. [DOI] [PubMed] [Google Scholar]
- Ringold G. M. Steroid hormone regulation of gene expression. Annu Rev Pharmacol Toxicol. 1985;25:529–566. doi: 10.1146/annurev.pa.25.040185.002525. [DOI] [PubMed] [Google Scholar]
- Russell D. H. Clinical relevance of polyamines. Crit Rev Clin Lab Sci. 1983;18(3):261–311. doi: 10.3109/10408368209085073. [DOI] [PubMed] [Google Scholar]
- Shen L. P., Rutter W. J. Sequence of the human somatostatin I gene. Science. 1984 Apr 13;224(4645):168–171. doi: 10.1126/science.6142531. [DOI] [PubMed] [Google Scholar]
- Sherman M. R., Stevens J. Structure of mammalian steroid receptors: evolving concepts and methodological developments. Annu Rev Physiol. 1984;46:83–105. doi: 10.1146/annurev.ph.46.030184.000503. [DOI] [PubMed] [Google Scholar]
- 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]
- Thomas T. J., Bloomfield V. A. Quasielastic laser light scattering and electron microscopy studies of the conformational transitions and condensation of poly(dA-dT).poly(dA-dT). Biopolymers. 1985 Dec;24(12):2185–2194. doi: 10.1002/bip.360241203. [DOI] [PubMed] [Google Scholar]
- Thomas T. J., Meryhew N. L., Messner R. P. DNA sequence and conformation specificity of lupus autoantibodies. Preferential binding to the left-handed Z-DNA form of synthetic polynucleotides. Arthritis Rheum. 1988 Mar;31(3):367–377. doi: 10.1002/art.1780310308. [DOI] [PubMed] [Google Scholar]
- Thomas T. J., Messner R. P. A left-handed (Z) conformation of poly(dA-dC).poly(dG-dT) induced by polyamines. Nucleic Acids Res. 1986 Aug 26;14(16):6721–6733. doi: 10.1093/nar/14.16.6721. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas T., Kiang D. T. Additive growth-inhibitory effects of DL-alpha-difluoromethylornithine and antiestrogens on MCF-7 breast cancer cell line. Biochem Biophys Res Commun. 1987 Nov 13;148(3):1338–1345. doi: 10.1016/s0006-291x(87)80279-6. [DOI] [PubMed] [Google Scholar]
- Thomas T., Kiang D. T. Effect of ribonuclease on the physico-chemical properties of estrogen receptor. J Steroid Biochem. 1985 Jul;23(1):19–25. doi: 10.1016/0022-4731(85)90255-9. [DOI] [PubMed] [Google Scholar]
- Thomas T., Kiang D. T. Ribonuclease-induced transformation of progesterone receptor from rabbit uterus. J Steroid Biochem. 1986 Feb;24(2):505–511. doi: 10.1016/0022-4731(86)90112-3. [DOI] [PubMed] [Google Scholar]
- Thomas T., Kiang D. T. Structural alterations and stabilization of rabbit uterine estrogen receptors by natural polyamines. Cancer Res. 1987 Apr 1;47(7):1799–1804. [PubMed] [Google Scholar]
- Thomas T., Leung B. S. Characterization of nuclear estradiol receptors released by micrococcal nuclease and deoxyribonuclease I. J Steroid Biochem. 1984 Jul;21(1):35–42. doi: 10.1016/0022-4731(84)90057-8. [DOI] [PubMed] [Google Scholar]
- Théveny B., Bailly A., Rauch C., Rauch M., Delain E., Milgrom E. Association of DNA-bound progesterone receptors. Nature. 1987 Sep 3;329(6134):79–81. doi: 10.1038/329079a0. [DOI] [PubMed] [Google Scholar]
- Weichman B. M., Notides A. C. Estradiol-binding kinetics of the activated and nonactivated estrogen receptor. J Biol Chem. 1977 Dec 25;252(24):8856–8862. [PubMed] [Google Scholar]
- Welshons W. V., Lieberman M. E., Gorski J. Nuclear localization of unoccupied oestrogen receptors. Nature. 1984 Feb 23;307(5953):747–749. doi: 10.1038/307747a0. [DOI] [PubMed] [Google Scholar]
- Yamamoto K. R. Steroid receptor regulated transcription of specific genes and gene networks. Annu Rev Genet. 1985;19:209–252. doi: 10.1146/annurev.ge.19.120185.001233. [DOI] [PubMed] [Google Scholar]
