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176 related items for PubMed ID: 9742103

  • 1. ADR1-mediated transcriptional activation requires the presence of an intact TFIID complex.
    Komarnitsky PB, Klebanow ER, Weil PA, Denis CL.
    Mol Cell Biol; 1998 Oct; 18(10):5861-7. PubMed ID: 9742103
    [Abstract] [Full Text] [Related]

  • 2. Dissection of the ADR1 protein reveals multiple, functionally redundant activation domains interspersed with inhibitory regions: evidence for a repressor binding to the ADR1c region.
    Cook WJ, Chase D, Audino DC, Denis CL.
    Mol Cell Biol; 1994 Jan; 14(1):629-40. PubMed ID: 8264631
    [Abstract] [Full Text] [Related]

  • 3. ADR1 activation domains contact the histone acetyltransferase GCN5 and the core transcriptional factor TFIIB.
    Chiang YC, Komarnitsky P, Chase D, Denis CL.
    J Biol Chem; 1996 Dec 13; 271(50):32359-65. PubMed ID: 8943299
    [Abstract] [Full Text] [Related]

  • 4. The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex.
    Drysdale CM, Jackson BM, McVeigh R, Klebanow ER, Bai Y, Kokubo T, Swanson M, Nakatani Y, Weil PA, Hinnebusch AG.
    Mol Cell Biol; 1998 Mar 13; 18(3):1711-24. PubMed ID: 9488488
    [Abstract] [Full Text] [Related]

  • 5. Mutations in the TATA-binding protein, affecting transcriptional activation, show synthetic lethality with the TAF145 gene lacking the TAF N-terminal domain in Saccharomyces cerevisiae.
    Kobayashi A, Miyake T, Ohyama Y, Kawaichi M, Kokubo T.
    J Biol Chem; 2001 Jan 05; 276(1):395-405. PubMed ID: 11035037
    [Abstract] [Full Text] [Related]

  • 6. Region of yeast TAF 130 required for TFIID to associate with promoters.
    Mencía M, Struhl K.
    Mol Cell Biol; 2001 Feb 05; 21(4):1145-54. PubMed ID: 11158301
    [Abstract] [Full Text] [Related]

  • 7. Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns.
    Kirschner DB, vom Baur E, Thibault C, Sanders SL, Gangloff YG, Davidson I, Weil PA, Tora L.
    Mol Cell Biol; 2002 May 05; 22(9):3178-93. PubMed ID: 11940675
    [Abstract] [Full Text] [Related]

  • 8. Characterization of a p53-related activation domain in Adr1p that is sufficient for ADR1-dependent gene expression.
    Young ET, Saario J, Kacherovsky N, Chao A, Sloan JS, Dombek KM.
    J Biol Chem; 1998 Nov 27; 273(48):32080-7. PubMed ID: 9822683
    [Abstract] [Full Text] [Related]

  • 9. Adr1 and Cat8 synergistically activate the glucose-regulated alcohol dehydrogenase gene ADH2 of the yeast Saccharomyces cerevisiae.
    Walther K, Schüller HJ.
    Microbiology (Reading); 2001 Aug 27; 147(Pt 8):2037-2044. PubMed ID: 11495982
    [Abstract] [Full Text] [Related]

  • 10. Specific interactions with TBP and TFIIB in vitro suggest that 14-3-3 proteins may participate in the regulation of transcription when part of a DNA binding complex.
    Pan S, Sehnke PC, Ferl RJ, Gurley WB.
    Plant Cell; 1999 Aug 27; 11(8):1591-602. PubMed ID: 10449590
    [Abstract] [Full Text] [Related]

  • 11. ADH2 expression is repressed by REG1 independently of mutations that alter the phosphorylation of the yeast transcription factor ADR1.
    Dombek KM, Camier S, Young ET.
    Mol Cell Biol; 1993 Jul 27; 13(7):4391-9. PubMed ID: 8321238
    [Abstract] [Full Text] [Related]

  • 12. Identification of highly conserved amino-terminal segments of dTAFII230 and yTAFII145 that are functionally interchangeable for inhibiting TBP-DNA interactions in vitro and in promoting yeast cell growth in vivo.
    Kotani T, Miyake T, Tsukihashi Y, Hinnebusch AG, Nakatani Y, Kawaichi M, Kokubo T.
    J Biol Chem; 1998 Nov 27; 273(48):32254-64. PubMed ID: 9822704
    [Abstract] [Full Text] [Related]

  • 13. Mechanisms of transcriptional activation and repression can both involve TFIID.
    Manley JL, Um M, Li C, Ashali H.
    Philos Trans R Soc Lond B Biol Sci; 1996 Apr 29; 351(1339):517-26. PubMed ID: 8735274
    [Abstract] [Full Text] [Related]

  • 14. Functional interaction of CCR4-NOT proteins with TATAA-binding protein (TBP) and its associated factors in yeast.
    Badarinarayana V, Chiang YC, Denis CL.
    Genetics; 2000 Jul 29; 155(3):1045-54. PubMed ID: 10880468
    [Abstract] [Full Text] [Related]

  • 15. Adenovirus E1A requires the yeast SAGA histone acetyltransferase complex and associates with SAGA components Gcn5 and Tra1.
    Kulesza CA, Van Buskirk HA, Cole MD, Reese JC, Smith MM, Engel DA.
    Oncogene; 2002 Feb 21; 21(9):1411-22. PubMed ID: 11857084
    [Abstract] [Full Text] [Related]

  • 16. Incorporation of Drosophila TAF110 into the yeast TFIID complex does not permit the Sp1 glutamine-rich activation domain to function in vivo.
    Keaveney M, Struhl K.
    Genes Cells; 1999 Apr 21; 4(4):197-203. PubMed ID: 10336691
    [Abstract] [Full Text] [Related]

  • 17. The histone H3-like TAF is broadly required for transcription in yeast.
    Moqtaderi Z, Keaveney M, Struhl K.
    Mol Cell; 1998 Nov 21; 2(5):675-82. PubMed ID: 9844639
    [Abstract] [Full Text] [Related]

  • 18. Glucose repression of the yeast ADH2 gene occurs through multiple mechanisms, including control of the protein synthesis of its transcriptional activator, ADR1.
    Vallari RC, Cook WJ, Audino DC, Morgan MJ, Jensen DE, Laudano AP, Denis CL.
    Mol Cell Biol; 1992 Apr 21; 12(4):1663-73. PubMed ID: 1549119
    [Abstract] [Full Text] [Related]

  • 19. yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex.
    Natarajan K, Jackson BM, Rhee E, Hinnebusch AG.
    Mol Cell; 1998 Nov 21; 2(5):683-92. PubMed ID: 9844640
    [Abstract] [Full Text] [Related]

  • 20. Yeast TAF(II)90 is required for cell-cycle progression through G2/M but not for general transcription activation.
    Apone LM, Virbasius CM, Reese JC, Green MR.
    Genes Dev; 1996 Sep 15; 10(18):2368-80. PubMed ID: 8824595
    [Abstract] [Full Text] [Related]

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