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Association of Purα and E2F-1 suppresses transcriptional activity of E2F-1

Abstract

Protein-protein interaction can play an important role in the control of several biological events including gene transcription, replication and cell proliferation. E2F-1 is a DNA-binding transcription factor which, upon interaction with its target DNA sequence, induces expression of several S phase specific genes allowing progression of the cell cycle. Evidently, the activity of this protein is modulated by its cellular partner, pRb, which in the hypophosphorylated form, binds to E2F-1 and inactivates its transcriptional ability. In this study, we have demonstrated that expression of a sequence-specific single-stranded DNA binding protein, Purα, in cells decreases the ability of E2F-1 to exert its transcriptional activity upon the responsive promoter derived from DHFR. Results from band shift experiments revealed that while Purα does not recognize the double-stranded DNA fragment containing the E2F-1 binding site, it has the ability to inhibit E2F-1 interaction with its target DNA sequence. Results from GST pull-down assays and the combined immunoprecipitation/Western blot analysis of nuclear extracts revealed a direct association of E2F-1 with Purα in the absence of the DNA molecule containing the E2F-1 binding site. The association of Purα with E2F-1 may increase the stability of E2F-1, as a higher level of E2F-1 was detected in cells co-expressing Purα and E2F-1. The importance of these observations with respect to the role of Purα in the control of cell cycle progression is discussed.

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References

  • Bergemann AD and Johnson EM. . 1992 Mol. Cell. Biol. 12: 1257–1265.

  • Bergemann AD, Ma ZW and Johnson EM. . 1992 Mol. Cell. Biol. 12: 5673–5682.

  • Chen NN and Khalili K. . 1995 J. Virol. 69: 5843–5848.

  • Chen NN, Chang CF, Gallia GL, Kerr DA, Johnson EM, Krachmarov CP, Barr SM, Frisque RJ, Bollag B and Khalili K. . 1995 Proc. Natl. Acad. Sci. USA 92: 1087–1091.

  • DeCaprio JA, Ludlow JW, Figge J, Shew JY, Huang CM, Lee WH, Marsillo E, Paucha E and Livingston DM. . 1988 Cell 54: 275–283.

  • Du Q, Tomkinson AE and Gardner PD. . 1997 J. Biol. Chem. 272: 14990–14995.

  • Graham FL and van der Eb AJ. . 1973 Virology 52: 456–467.

  • Haas S, Thatikunta P, Steplewski A, Johnson EM, Khalili, K and Amini S. . 1995 J. Cell. Biol. 130: 1171–1179.

  • Johnson EM, Chen PL, Krachmarov CP, Barr SM, Kanovsky M, Ma ZW and Lee WH. . 1995 J. Biol. Chem. 270: 24352–24360.

  • Kelm RJ, Elder PK, Strauch AR and Getz MJ. . 1997 J. Biol. Chem. 272: 26727–26733.

  • Krachmarov CP, Chepenik LG, Barr-Vagell S, Khalili K and Johnson EM. . 1996 Proc. Natl. Acad. Sci. USA 93: 14112–14117.

  • Kundu M, Guermah M, Roeder RG, Amini S and Khalili K. . 1997 J. Biol. Chem. 272: 29468–29474.

  • LaThangue NB. . 1994 Curr. Opin. Cell Biol. 6: 443–450.

  • Ma ZW, Bergemann AD and Johnson EM. . 1994 Gene 149: 311–314.

  • Nevins JR. . 1992 Science 258: 424–429.

  • Weinberg RA. . 1995 Cell 81: 323–330.

  • Zambrano N, DeRenzis S, Minopoli G, Faraonio R, Donini V, Scaloni A, Cimino F and Russo T. . 1997 Biochem. J. 328: 293–300.

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Acknowledgements

We wish to thank all past and present members of the Center for NeuroVirology and NeuroOncology for sharing of ideas and reagents. We also thank Cynthia Schriver for editorial assistance. This work was made possible by grants awarded by NIH to K Khalili.

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Darbinian, N., Gallia, G., Kundu, M. et al. Association of Purα and E2F-1 suppresses transcriptional activity of E2F-1. Oncogene 18, 6398–6402 (1999). https://doi.org/10.1038/sj.onc.1203011

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