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The glucocorticoid receptor precludes the binding of a transcriptional repressor protein to the long terminal repeat of the mouse mammary tumor virus

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Abstract

The long terminal repeat (LTR) of the mouse mammary tumor virus was used as a template to examine the dual binding parameters of the glucocorticoid-receptor (GR) and a repressor protein termed Inhibitory Factor 1 (IF1). The roceptor binds specifically to the glucocorticoid response element and precludes the binding of IF1 to its juxtaposed binding site within the LTR. When the two DNA targets are separated by the insertion of an additional 52 base pairs, coincident binding of both proteins is observed. Gel retention assays reveal three distinct nucleoprotein complexes. The first complex consists of the receptor and the LTR, the second is comprised of IF1 and DNA and the third is a multiprotein-DNA complex consisting of the GR, IF1 and DNA, migrating at a higher molecular weight position. The inhibition of IF1 binding by the presence of prebound GR leads to the repression of transcription of juxtaposed genes. The GR may act to block access of a sequence, used by the cell to titrate repressor proteins and facilitate the onset of gene expression. (Mol Cell Biochem122: 25–37, 1993)

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References

  1. Majors J: The structure and function of retroviral long terminal repeats. Curr Top Micro 157: 50–59, 1990

    Google Scholar 

  2. Lee F, Mulligan R, Berg P, Ringold G: Glucocorticoids regulate expression of dihydrofolate reductase cDNA in a mouse mammary tumor virus chimaeric plasmids. Nature 294: 228–232, 1981

    Google Scholar 

  3. Huang AL, Ostrowski MC, Berard D, Hager GL: Glucocorticoid regulation of the Ha-MuSV p21 gene conferred by sequences from mouse mammary tumor virus Cell 27: 245–255, 1981

    Google Scholar 

  4. Yamamoto KR: Steroid receptor regulated transcription of specific genes and gene networks. Ann Rev Genet 19: 209–252, 1985

    Google Scholar 

  5. Cordingley MG, Riegel AT, Hager GL: Steroid-dependent interaction of transcription factors with the inducible promoter of mouse mammary tumor virusin vivo. Cell 48: 261–270, 1987

    Google Scholar 

  6. Kuo W-L, Vilander LR, Huang M, Peterson DO: A transcriptionally defective long terminal repeat within an endogenous copy of mouse mammary tumor virus proviral DNA. J Virol 62: 2394–2402, 1988

    Google Scholar 

  7. Richard-Foy H, Hager GL: Sequence-specific positioning over the steroid inducible MMTV promoter. EMBO J 6: 2321–2328, 1987

    Google Scholar 

  8. Perlmann T, Wrange O: Specific glucocorticoid receptor binding to DNA reconstituted in a nucleosome. EMBO J 7: 3073–3079, 1988

    Google Scholar 

  9. Piña B, Brüggemeier U, Beato M: Nucleosome positioning modulates accessibility of regulatory proteins to the mouse mammary tumor virus promoter Cell 60: 719–731, 1990

    Google Scholar 

  10. Archer TK, Cordingley MG, Wolford RG, Hager GL: Transcription factor access is mediated by accurately positioned nucleosomes on the mouse mammary tumor virus promoter. Mol Cell Biol 11 2: 688–698, 1991

    Google Scholar 

  11. Li H-L, Kmiec EB: A glucocorticoid response element enhances transcription of a methionine tRNA genein cis andtrans. Mol Endo 4: 1173–1182, 1990

    Google Scholar 

  12. Sekiguchi JM, Kmiec EB:Cis-acting enhancement of RNA polymerase III gene expressionin vitro. Mol Gen Genet 221: 435–442, 1990

    Google Scholar 

  13. Carballo M, Beato M: Binding of glucocorticoid receptor induces a topological change in plasmids containing the hormone response element of mouse mammary tumor virus. DNA and Cell Biol 9: 519–525, 1990

    Google Scholar 

  14. Perlmann T: Glucocorticoid receptor DNA binding specificity is increased by the organization of DNA in nucleosomes. Proc Natl Acad Sci USA 89: 3884–3888, 1992

    Google Scholar 

  15. Ruberti I, Worcel A: Mechanism of chromatin assembly in Xenopus oocytes. J Mol Biol 189: 457–476, 1986

    Google Scholar 

  16. Crosten GE, Kerrigan LA, Lira LM, Marshak DR, Kadonaga JT: Sequence-specific antirepression of histone H1-mediated inhibition of basal RNA polymerase II transcription. Science 251: 643–650, 1991

    Google Scholar 

  17. Diamond M, Miner JN, Yoshinaga SK, Yamamoto KR: Transcription factor interactions: Selectors of positive or negative regulation from a single DNA element. Science 249: 1266–1272, 1990

    Google Scholar 

  18. Siddique HR, Sarkar NH: The interaction of a c-jun/fos related protein factor with the U3 sequences of the mouse mammary tumor virus LTR. Bioch Biophys Rsch Comm 172: 348–360, 1990

    Google Scholar 

  19. Miner JN, Yamamoto KR: Regulatory crosstalk at composite response elements. TIBS 16: 423–426, 1991

    Google Scholar 

  20. Peterson DL, Beifuss K, Morely KL: Context-dependent gene expression:Cis-acting negative effects of specific plasmid sequences on eukaryotic genes. Mol Cell Biol 7: 1563–1567, 1987

    Google Scholar 

  21. Razvi F, Garguilo G, Worcel A: A simple procedure for parallel sequence analysis of both strands of 5′-labeled DNA. Gene 23: 175–183, 1983

    Google Scholar 

  22. Sekiguchi JM, Swank RA, Kmiec EB: Changes in DNA topology can modulatein vitro transcription of certain RNA polymerase III genesin vitro. Mol Cell Biochem 85: 123–133, 1989

    Google Scholar 

  23. Glikin G, Ruberti I, Worcel A: Chromatin assembly in Xenopus oocytes:In vitro studies. Cell 37: 33–41, 1984

    Google Scholar 

  24. Kmiec EB, Sekiguchi JM, Cole AD: Studies on the ATP requirement ofin vitro chromatin assembly. Biochem Cell Biol 67: 443–454, 1989

    Google Scholar 

  25. Sinden RR, Carlson JO, Pettijohn DE: Torsional tension in the DNA helix measured with trimethyl psoralen in livingE. coli cells: Analogous measurements in insects and human cells. Cell 21: 773–783

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Ye, S., Kmiec, E.B. The glucocorticoid receptor precludes the binding of a transcriptional repressor protein to the long terminal repeat of the mouse mammary tumor virus. Mol Cell Biochem 122, 25–37 (1993). https://doi.org/10.1007/BF00925734

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  • DOI: https://doi.org/10.1007/BF00925734

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