Estrogen treatment induces elevated expression of HMG1 in MCF-7 cells

Experimental Cell Research

Volumn 241, Issue 1, 1998, Pages 269-272

  Chau, K Y ^a,b,c   Lam, H Y Peter ^b   Lee, K L Daniel ^a  

^a HONG KONG POLYTECHNIC UNIVERSITY   (Hong Kong)

^b HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

^c SCHEPENS EYE RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ESTROGEN; HIGH MOBILITY GROUP PROTEIN;

ARTICLE; CELL STRAIN MCF 7; ESTROGEN ACTIVITY; HORMONAL REGULATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SYNTHESIS REGULATION;

EUKARYOTA; MINK CELL FOCUS-FORMING VIRUS;

EID: 0031843859     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1998.4052     Document Type: Article

References (25)

1. II30 affect estrogen receptor-mediated transcriptional activation. Mol. Endocrinol. 11(8), 1009-1019.
2. Tremethick, D. J., and Molloy, P. L. (1986). High mobility group proteins 1 and 2 stimulates transcription in vitro by RNA polymeerase II and III. J. Biol. Chem. 261(15), 6986-6992.
3. Waga, S., Mizuno, S., and Yoshida, M. (1990). Chromosomal protein HMG1 removes the transcriptional block caused by the cruciform in supercolied DNA. J. Biol. Chem. 265(32), 19424-19428.
4. Varga-Weisz, P., van Holde, K., and Zlatanova, J. (1994). Competition between linker histones and HMG1 for binding to fourway junction DNA: Implications for transcription. Biochem. Biophys. Res. Commun. 203(3), 1904-1911.
5. Ogawa, Y., Aizawa, S., Shirakawa, H., and Yoshida, M. (1995). Stimulation of transcription accompanying relaxation of chromatin structure in cells overexpressing high mobility group 1 protein. J. Biol. Chem. 270(16), 9272-9280.
6. Kato, Y., and Iwai, K. (1984). An approach to searching for specific proteins associated with active genes in hen oviduct. Endocrinol. Jpn. 31(4), 509-522.
7. Guo, J. Z., and Gorski, J. (1988). Differential stimulation of histone and high mobility group chromatin protein synthesis in the rat uterus by estrogen. Mol. Endocrinol. 2(8), 686-692.
8. Kumar, V., and Chambon, P. (1998). The estrogen receptor binds tightly to its responsive element as a ligand-induced homodimer. Cell 55, 145-156.
9. Lannigan, D. A., and Notides, A. C. (1989). Estrogen receptor selectively binds the "coding strand" of an estrogen responsive element. Proc. Natl. Acad. Sci. USA 86, 863-867.
10. Feavers, I. M., Jiricny, J., Moncharmont, B., Saluz, H. P., and Jost, J. P. (1987). Interaction of two nonhistone proteins with the estradiol response element of the avian vitellogenin gene modulates the binding of estradiol-receptor complex. Proc. Natl. Acad. Sci. USA 84, 7453-7457.
11. Mukherjee, R., and Chambon, P. (1990). A single-stranded DNA-binding protein promotes the binding of the purified oestrogen receptor to its responsive element. Nucleic Acids Res. 18(19), 5713-5716.
12. Edwards, D. P., Kuhnel, B., Estes, P. A., and Nordeen, S. K. (1989). Human progesterone receptor binding to mouse mammary tumor virus deoxyribonucleic acid: Dependence on hormone and nonreceptor nuclear factor(s). Mol. Endocrinol. 3(2), 381-391.
13. Prendergast, P., Onate, S. A., Christensen, K., and Ewards, D. P. (1994). Nuclear accessory factors enhance the binding of progesterone receptor to specific target DNA. J. Steroid Biochem. Molec. Biol. 48(1), 1-13.
14. Chomczynski, P., and Sacchi, N. (1987). Single-step method of RNA isolation by acid guanidinum thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162, 156-159.
15. Lee, K.-L. D., Pentecost, B. T., D'Anna, J. A., Tobey, R. A., Gurley, L. R., and Dixon, G. H. (1987). Characterization of cDNA sequences corresponding to three distinct HMG-1 mRNA species in line CHO Chinese hamster cells and cell cycle expression of the HMG-1 gene. Nucleic Acids Res. 15(13), 5051-5068.
16. Lam, H. Y., Ng, P. K., Goldenberg, G. J., and Wong, C. M. (1987). Estrogen receptor-binding affinity and cytotoxic activity of three new estrogen-nitrosourea conjugates in human cancer cell lines in vitro. Cancer Treat. Rep. 71(10), 901-906.
17. Jantzen, H. M., Admon, A., Bell, S. P., and Tjian, R. (1990). Nucleolar transcription factor hUBF contains a DNA-binding motif with homology to HMG proteins. Nature 344, 830-836.
18. Sinclair, A. H., Berta, P., Palmer, M. S., Hawkins, J. R., Griffiths, B. L., Smith, M. J., Foster, J. W., Frischauf, A.-M., Lovell-Badge, R., and Goodfellow, P. N. (1990). A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 346, 240-244.
19. Milatovich, A., Travis, A., Grosschedl, R., and Francke, U. (1991). Gene for lymphoid enhancer-binding factor (LEF1) mapped to human chromosome 4)q23-25) and mouse chromosome 3 near Egf. Genomics 11, 1040-1048.
20. Pil, P. M., Chow, C. S., and Lippard, S. J. (1993). High-mobility-group 1 protein mediates DNA bending as determined by ring closures. Proc. Natl. Acad. Sci. USA 90, 9465-9469.
21. Nardulli, A. M., and Shapiro, D. J. (1992). Binding of the estrogen receptor DNA-binding domain to the estrogen response element induces DNA bending. Mol. Cell. Biol. 12(5), 2037-2042.
22. Nardulli, A. M., and Shapiro, D. J. (1993). DNA bending by Nuclear receptors. Receptor 3, 247-255.
23. Onate, S. A., Prendergast, P., Wagner, J. P., Nissen, M., Reeves, R., Pettijohn, D. E., and Edwards, D. P. (1994). The DNA-bending protein HMG-1 enhances progesterone receptor binding to its target DNA sequences. Mol. Cell. Biol. 14(5), 3367-3391.
24. Glass, C. K., Rose, D. W., and Rosenfeld, G. (1997). Nuclear receptor coactivators. Curr. Opin. Cell Biol. 9, 222-232.
25. Katzenellenbogen, J. A., and Katzenellenbogen, B. B. (1996). Nuclear hormone receptors: Ligand-activated regulators of transcription and diverse cell responses. Chem. Biol. 3, 529-536.