Functional Distinctions between Yeast TATA Elements

LITERATURE CITED

• Arcangioli, B., and B. Lescure. 1985. Identification of proteins involved in the regulation of yeast iso-l-cytochrome c expression by oxygen. EMBO J. 4:2627–2633.
   PubMedGoogle Scholar
• Arndt, K. T., C. Styles, and G. R. Fink. 1987. Multiple global regulators control HIS4 transcription in yeast. Science 237:874–880.
   PubMedGoogle Scholar
• Bohmann, D., T. J. Bos, A. Admon, T. Nishimura, P. K. Vogt, and R. Tjian. 1987. Human proto-oncogene c-jun encodes a DNA binding protein with structural and functional properties of transcription factor AP-1. Science 238:1386–1392.
   PubMed Web of Science ®Google Scholar
• Brandl, C. J., and K. Struhl. 1989. Yeast GCN4 transcriptional activator protein interacts with RNA polymerase II in vitro. Proc. Natl. Acad. Sci. USA 86:2652–2656.
   PubMedGoogle Scholar
• Breathnach, R., and P. Chambon. 1981. Organization and expression of eukaryotic split genes coding for proteins. Annu. Rev. Biochem. 50:349–383.
   PubMed Web of Science ®Google Scholar
• Brent, R., and M. Ptashne. 1985. A eukaryotic transcriptional activator bearing the DNA specificity of a prokaryotic repressor. Cell 43:729–736.
   PubMed Web of Science ®Google Scholar
• Chen, W., and K. Struhl. 1988. Saturation mutagenesis of a yeast his3 TATA element: genetic evidence for a specific TATA-binding protein. Proc. Natl. Acad. Sci. USA 85:2691–2695.
   PubMed Web of Science ®Google Scholar
• Chen, W., and K. Struhl. 1989. Yeast upstream activator protein GCN4 can stimulate transcription when its binding site replaces the TATA element. EMBO J. 8:261–268.
   PubMedGoogle Scholar
• Davidson, I., J. H. Xiao, R. Rosales, A. Staub, and P. Chambon. 1988. The HeLa cell protein TEF-1 binds specifically and cooperatively to two SV40 enhancer motifs of unrelated sequence. Cell 54:931–942.
   PubMedGoogle Scholar
• Davison, B. L., J.-M. Egly, E. R. Mulvihill, and P. Chambon. 1983. Formation of stable preinitiation complexes between eukaryotic class B transcription factors and promoter sequences. Nature (London) 301:680–686.
   PubMed Web of Science ®Google Scholar
• Dorn, A., J. Bollekens, A. Staub, C. Benoist, and D. Mathis. 1987. A multiplicity of CCAAT box-binding proteins. Cell 50:863–872.
   PubMed Web of Science ®Google Scholar
• Gill, G., and G. Ptashne. 1988. Negative effect of the transcriptional activator GAL4. Nature (London) 334:721–723.
   PubMed Web of Science ®Google Scholar
• Giiarente, L.. 1988. UASs and enhancers: common mechanism of transcriptional activation in yeast and mammals. Cell 52:303–305.
   PubMedGoogle Scholar
• Heimann, J. D., and M. J. Chamberlin. 1988. Structure and function of bacterial sigma factors. Annu. Rev. Biochem. 57:839–872.
   PubMedGoogle Scholar
• Hinnebusch, A. G.. 1984. Evidence for translational regulation of the activator of general amino acid control in yeast. Proc. Natl. Acad. Sci. USA 81:6442–6446.
   PubMed Web of Science ®Google Scholar
• Homa, F. L., J. C. Glorioso, and M. Levine. 1988. A specific 15-bp TATA box promoter element is required for expression of a herpes simplex virus type I late gene. Genes Dev. 2:40–53.
   PubMed Web of Science ®Google Scholar
• Hope, I. A., and K. Strubl. 1985. GCN4 protein, synthesized in vitro, binds to HIS3 regulatory sequences: implications for the general control of amino acid biosynthetic genes in yeast. Cell 43:177–188.
   PubMed Web of Science ®Google Scholar
• Hope, I. A., and K. Strubl. 1986. Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast. Cell 46:885–894.
   PubMed Web of Science ®Google Scholar
• Johnson, A. D., A. R. Poteete, G. Lauer, R. T. Sauer, G. R. Ackers, and M. Ptashne. 1981. λ repressor and cro- components of an efficient molecular switch. Nature (London) 294:217–223.
   PubMed Web of Science ®Google Scholar
• Johnson, P. F., and S. L. McKnight. 1989. Eukaryotic transcriptional regulatory proteins. Annu. Rev. Biochem. 58:799–839.
   PubMed Web of Science ®Google Scholar
• Jones, K. A., J. T. Kadonaga, P. J. Rosenfeld, T. J. Kelly, and R. Tjian. 1987. A cellular DNA-binding protein that activates eukaryotic transcription and DNA replication. Cell 48:79–89.
   PubMed Web of Science ®Google Scholar
• Landschulz, W. H., P. F. Johnson, and S. L. McKnight. 1988. The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins. Science 240:1759–1764.
   PubMed Web of Science ®Google Scholar
• Ma, J., and M. Ptashne. 1987. Deletion analysis of GAL4 defines two transcriptional activating segments. Cell 48:847–853.
   PubMed Web of Science ®Google Scholar
• Moye-Rowley, W. S., K. D. Harshman, and C. S. Parker. 1989. Yeast YAP1 encodes a novel form of the jun family of transcriptional activator proteins. Genes Dev. 3:283–292.
   PubMed Web of Science ®Google Scholar
• Oliphant, A. R., A. L. Nussbaum, and K. Struhl. 1986. Cloning of random-sequence oligodeoxynucleotides. Gene 44:177–183.
   PubMed Web of Science ®Google Scholar
• Parker, C. S., and J. Topol. 1984. A Drosophila RNA polymer ase II transcription factor contains a promoter-region specific DNA-binding activity. Cell 36:357–369.
   PubMed Web of Science ®Google Scholar
• Pfeifer, K., B. Arcangiolo, and L. Guarente. 1987. Yeast HAP1 activator competes with the factor RC2 for binding to the upstream activator site UAS1 of the CYC1 gene. Cell 49:9–18.
   PubMed Web of Science ®Google Scholar
• Pfeifer, K., T. Prezant, and L. Guarente. 1987. Yeast HAP1 activator binds to two upstream activation sites of different sequence. Cell 49:19–27.
   PubMedGoogle Scholar
• Rauscher, F. J., III, D. R. Cohen, T. Curran, T. J. Bos, P. K. Vogt, D. Bohmann, R. Tjian, and B. R. Franza. 1988. Fos-associated protein p39 is the product of the jun proto-oncogene. Science 240:1010–1016.
   PubMed Web of Science ®Google Scholar
• Ryder, K., L. F. Lau, and D. Nathans. 1988. A gene activated by growth factors is related to the oncogene v-jun. Proc. Natl. Acad. Sci. USA 85:1487–1491.
   PubMed Web of Science ®Google Scholar
• Sakai, D. D., S. Helms, J. Carlstedt-Duke, J.-A. Gustafsson, F. M. Rottman, and K. R. Yamamoto. 1988. Hormone-mediated repression: a negative glucocorticoid response element from the bovine prolactin gene. Genes Dev. 2:1144–1154.
   PubMed Web of Science ®Google Scholar
• Sawadogo, M., and R. G. Roeder. 1985. Interaction of a genespecific transcription factor with the adenovirus major late promoter upstream of the TATA box region. Cell 43:165–175.
   PubMed Web of Science ®Google Scholar
• 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 El A regulation. Cell 52:723–729.
   PubMedGoogle Scholar
• Struhl, K.. 1982. Regulatory sites for his3 expression in yeast. Nature (London) 300:284–287.
   Web of Science ®Google Scholar
• Struhl, K.. 1985. Naturally occuring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast. Proc. Natl. Acad. Sci. USA 82:8419–8423.
   PubMed Web of Science ®Google Scholar
• Struhl, K.. 1987. The DNA-binding domains of the jun oncoprotein and the yeast GCN4 transcriptional activator are functionally homologous. Cell 50:841–846.
   PubMedGoogle Scholar
• Struhl, K.. 1986. Constitutive and inducible Saccharomyces cerevisiae promoters: evidence for two distinct molecular mechanisms. Mol. Cell. Biol. 6:3847–3853.
   PubMedGoogle Scholar
• Struhl, K.. 1989. Molecular mechanisms of transcriptional regulation in yeast. Annu. Rev. Biochem. 58:1051–1077.
   PubMedGoogle Scholar
• Thireos, G., M. D. Penn, and H. Greer. 1984. 5′ untranslated sequences are required for the translational control of a yeast regulatory gene. Proc. Natl. Acad. Sci. USA 81:5096–5100.
   PubMed Web of Science ®Google Scholar