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Transcriptional Regulation

TFII-I Regulates Vβ Promoter Activity through an Initiator Element

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Pages 4444-4454 | Received 25 Feb 1998, Accepted 08 May 1998, Published online: 27 Mar 2023

REFERENCES

  • Anderson, S. J., H. S. Chou, and D. Y. Loh 1988. A conserved sequence in the T-cell receptor β-chain promoter region. Proc. Natl. Acad. Sci. USA 85: 3551–3554.
  • Anderson, S. J., S. Miyake, and D. Y. Loh 1989. Transcription from a murine T-cell receptor Vβ promoter depends on a conserved decamer motif similar to the cyclic AMP response element. Mol. Cell. Biol. 9: 4835–4845.
  • Burke, T. W., and J. T. Kadonaga 1996. Drosophila TFIID binds to a conserved downstream basal promoter element that is present in many TATA-box-deficient promoters. Genes Dev. 10: 711–724.
  • Burke, T. W., and J. T. Kadonaga 1997. The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila. Genes Dev. 11: 3020–3031.
  • Burley, S. K., and R. G. Roeder 1996. Biochemistry and structural biology of transcription factor IID (TFIID). Annu. Rev. Biochem. 65: 769–799.
  • Conaway, R. C., and J. W. Conaway 1993. General initiation factors for RNA polymerase II. Annu. Rev. Biochem. 62: 161–190.
  • Das, G., C. S. Hinkley, and W. Herr 1995. Basal promoter elements as a selective determinant of transcriptional activator function. Nature 374: 657–660.
  • Dignam, J. D., P. Martin, B. Shastry, and R. G. Roeder 1983. Eukaryotic gene transcription with purified components. Methods Enzymol. 101: 583–598.
  • Eichbaum, Q. G., R. Iyer, D. P. Raveh, C. Mathieu, and A. B. Ezekowitz 1994. Restriction of interferon γ responsiveness and basal expression of the myeloid human FcγR1b gene is mediated by a functional Pu.1 site and a transcriptional initiator (Inr) consensus. J. Exp. Med. 179: 1985–1986.
  • Fong, T. C., and B. M. Emerson 1992. The erythroid-specific protein cGATA-1 mediates distal enhancer activity through a specialized β-globin TATA box. Genes Dev. 6: 521–532.
  • Frankel, A. D., and P. S. Kim 1991. Modular structure of transcription factors: implications for gene regulation. Cell 65: 717–719.
  • Garraway, I. R., K. Semple, and S. T. Smale 1996. Transcription of the lymphocyte-specific terminal deoxynucleotidyltransferase gene requires a specific core promoter structure. Proc. Natl. Acad. Sci. USA 93: 4336–4341.
  • Gill, G. 1994. Transcriptional initiation: taking the initiative. Curr. Biol. 4: 374–376.
  • Grayson, J., R. S. Williams, Y. T. Yu, and R. Bassel-Duby 1995. Synergistic interactions between heterologous upstream activation elements and specific TATA sequences in a muscle-specific promoter. Mol. Cell. Biol. 15: 1870–1878.
  • Grueneberg, D. A., R. W. Henry, A. Brauer, C. D. Novina, V. Cheriyath, A. L. Roy, and M. Gilman 1997. A multifunctional DNA-binding protein that promotes the formation of serum response factor/homeodomain complexes: identity to TFII-I. Genes Dev. 11: 2482–2493.
  • Halle, J.-P., P. Haus-Seuffert, C. Woltering, G. Stelzer, and M. Meisterernst 1997. A conserved tissue-specific structure at a human T-cell receptor β-chain core promoter. Mol. Cell. Biol. 17: 4220–4229.
  • Hansen, S. K., and R. Tjian 1995. TAFs and TFIIA mediate differential utilization of the tandem Adh promoters. Cell 82: 565–575.
  • Herskowitz, I. 1987. Functional inactivation of genes by dominant negative mutations. Nature 329: 219–222.
  • Hope, I. A., and K. Struhl 1986. Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast. Cell 46: 885–894.
  • Hubbard, S. J., F. Eisenmonger, and J. M. Thornton 1994. Modeling studies of the change in conformation required for cleavage of limited proteolysis sites. Protein Sci. 3: 757–768.
  • Javahery, R., A. Khachi, K. Lo, B. Zenzie-Gregory, and S. T. Smale 1994. DNA sequence requirements for transcriptional initiator activity in mammalian cells. Mol. Cell. Biol. 14: 116–127.
  • Johansson, E., E. Skogman, and L. Thelander 1995. The TATA-less promoter of mouse ribonucleotide reductase R1 gene contains a TFII-I binding initiator element essential for cell cycle-regulated transcription. J. Biol. Chem. 270: 30162–30167.
  • Jonsen, M. D., J. M. Petersen, Q.-P. Xu, and B. J. Graves 1996. Characterization of the cooperative function of inhibitory sequences in Ets-1. Mol. Cell. Biol. 16: 2065–2073.
  • Kaufmann, J., C. P. Verrijzer, J. Shao, and S. T. Smale 1996. CIF, an essential cofactor for TFIID-dependent initiator function. Genes Dev. 10: 873–886.
  • Kaufmann, J., K. Ahrens, R. Koop, S. T. Smale, and R. Muller 1998. CIF150, a human cofactor for transcription factor IID-dependent initiator function. Mol. Cell. Biol. 18: 233–239.
  • Kim, D.-W., V. Cheriyath, A. L. Roy, and B. H. Cochran 1998. TFII-I enhances activation of the c-fos promoter through interactions with upstream elements. Mol. Cell. Biol. 18: 3310–3320.
  • Luo, X., and M. Sawadogo 1996. Functional domains of the transcription factor USF2: atypical nuclear localization signals and context-dependent transcriptional activation domains. Mol. Cell. Biol. 16: 1367–1375.
  • Ma, J., and M. Ptashne 1987. Deletion analysis of GAL4 defines two transcriptional activating segments. Cell 48: 847–853.
  • Manzano-Winkler, B., C. D. Novina, and A. L. Roy 1996. TFII-I is required for transcription of the naturally TATA-less but initiator-containing Vβ promoter. J. Biol. Chem. 271: 12076–12081.
  • Martinez, E., C. M. Chiang, H. Ge, and R. G. Roeder 1994. TAFs in TFIID function through the initiator to direct basal transcription from a TATA-less class II promoter. EMBO J. 13: 3115–3126.
  • Novina, C. D., and A. L. Roy 1996. Core promoter mediated transcription. Trends Genet. 12: 351–355.
  • Novina, C. D., V. Cheriyath, M. C. Denis, and A. L. Roy 1997. Methods for studying the biochemical properties of an Inr element binding protein: TFII-I. Methods 12: 254–263.
  • Orphanides, G., T. Lagrange, and D. Reinberg 1996. The general transcription factors of RNA polymerase II. Genes Dev. 10: 2657–2683.
  • Perez-Jurado, L. A., Y.-K. Wang, R. Peoples, A. Coloma, J. Cruces, and U. Francke 1998. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of Btk. Hum. Mol. Genet. 7: 325–334.
  • Ptashne, M., and A. Gann 1997. Transcriptional activation by recruitment. Nature 386: 569–577.
  • Roeder, R. G. 1996. The role of general initiation factors in transcription by RNA polymerase II. Trends Biochem. 21: 327–335.
  • Roy, A. L., M. Meisterernst, P. Pognonec, and R. G. Roeder 1991. Cooperative interaction of an initiator-binding transcription initiation factor and the helix-loop-helix activator USF. Nature 354: 245–248.
  • Roy, A. L., S. Malik, M. Meisterernst, and R. G. Roeder 1993. An alternative pathway for transcription initiation involving TFII-I. Nature 365: 355–359.
  • Roy, A. L., H. Du, P. D. Gregor, C. D. Novina, E. Martinez, and R. G. Roeder 1997. Cloning of an Inr- and E-box-binding protein, TFII-I, that interacts physically and functionally with USF1. EMBO J. 16: 7091–7104.
  • Simon, M. C., T. M. Fisch, B. J. Benecke, J. R. Nevins, and N. Heintz 1988. Definition of multiple, functionally distinct TATA elements, one of which is a target in the hsp70 promoter for E1A regulation. Cell 52: 723–729.
  • Smale, S. T., and D. Baltimore 1989. The “initiator” as a transcription control element. Cell 57: 103–113.
  • Smale, S. T., M. C. Schmidt, A. J. Berk, and D. Baltimore 1990. Transcriptional activation by Sp1 as directed through TATA or initiator: specific requirements for mammalian transcription factor IID. Proc. Natl. Acad. Sci. USA 87: 4509–4513.
  • Smale, S. T. 1997. Transcription initiation from TATA-less promoters within eukaryotic protein-coding genes. Biochim. Biophys. Acta 1351: 73–88.
  • Tanaka, M., R. Gupta, and B. J. Mayer 1995. Differential inhibition of signaling pathways by dominant-negative SH2/SH3 adapter proteins. Mol. Cell. Biol. 15: 6829–6837.
  • Triezenberg, S. J. 1995. Structure and function of transcriptional activation domains. Curr. Opin. Genet. Dev. 5: 190–195.
  • Verrijzer, C. P., J. L. Chen, K. Yokomori, and R. Tjian 1995. Binding of TAFs to core elements directs promoter selectivity by RNA polymerase II. Cell 81: 1115–1125.
  • Verrijzer, C. P., and R. Tjian 1996. TAFs mediate transcriptional activation and promoter selectivity. Trends Biochem. 21: 338–342.
  • Wefald, F. C., B. H. Devlin, and R. S. Williams 1990. Functional heterogeneity of mammalian TATA-box sequences revealed by interaction with a cell-specific enhancer. Nature 344: 260–262.
  • Weis, L., and D. Reinberg 1997. Accurate positioning of RNA polymerase II on a natural TATA-less promoter is independent of TATA-binding-protein-associated factors and initiator-binding proteins. Mol. Cell. Biol. 17: 2973–2984.
  • Yang, W., and S. Desiderio 1997. BAP-135, a target for Bruton’s tyrosine kinase in response to B cell receptor engagement. Proc. Natl. Acad. Sci. USA 94: 604–609.

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