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Journal Abstract Search

876 related items for PubMed ID: 29176831

  • 21. A transcription factor IIA-binding site differentially regulates RNA polymerase II-mediated transcription in a promoter context-dependent manner.
    Wang J, Zhao S, He W, Wei Y, Zhang Y, Pegg H, Shore P, Roberts SGE, Deng W.
    J Biol Chem; 2017 Jul 14; 292(28):11873-11885. PubMed ID: 28539359
    [Abstract] [Full Text] [Related]

  • 22. Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID.
    Warfield L, Ramachandran S, Baptista T, Devys D, Tora L, Hahn S.
    Mol Cell; 2017 Oct 05; 68(1):118-129.e5. PubMed ID: 28918900
    [Abstract] [Full Text] [Related]

  • 23. Genome-wide localization analysis of a complete set of Tafs reveals a specific effect of the taf1 mutation on Taf2 occupancy and provides indirect evidence for different TFIID conformations at different promoters.
    Ohtsuki K, Kasahara K, Shirahige K, Kokubo T.
    Nucleic Acids Res; 2010 Apr 05; 38(6):1805-20. PubMed ID: 20026583
    [Abstract] [Full Text] [Related]

  • 24. Saccharomyces cerevisiae HMO1 interacts with TFIID and participates in start site selection by RNA polymerase II.
    Kasahara K, Ki S, Aoyama K, Takahashi H, Kokubo T.
    Nucleic Acids Res; 2008 Mar 05; 36(4):1343-57. PubMed ID: 18187511
    [Abstract] [Full Text] [Related]

  • 25. Distinct role of Mediator tail module in regulation of SAGA-dependent, TATA-containing genes in yeast.
    Ansari SA, Ganapathi M, Benschop JJ, Holstege FC, Wade JT, Morse RH.
    EMBO J; 2012 Jan 04; 31(1):44-57. PubMed ID: 21971086
    [Abstract] [Full Text] [Related]

  • 26. An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription.
    Walker AK, Shi Y, Blackwell TK.
    J Biol Chem; 2004 Apr 09; 279(15):15339-47. PubMed ID: 14726532
    [Abstract] [Full Text] [Related]

  • 27. Kin28 depletion increases association of TFIID subunits Taf1 and Taf4 with promoters in Saccharomyces cerevisiae.
    Knoll ER, Zhu ZI, Sarkar D, Landsman D, Morse RH.
    Nucleic Acids Res; 2020 May 07; 48(8):4244-4255. PubMed ID: 32182349
    [Abstract] [Full Text] [Related]

  • 28. The TATA box regulates TATA-binding protein (TBP) dynamics in vivo.
    Tora L, Timmers HT.
    Trends Biochem Sci; 2010 Jun 07; 35(6):309-14. PubMed ID: 20176488
    [Abstract] [Full Text] [Related]

  • 29. The new core promoter element XCPE1 (X Core Promoter Element 1) directs activator-, mediator-, and TATA-binding protein-dependent but TFIID-independent RNA polymerase II transcription from TATA-less promoters.
    Tokusumi Y, Ma Y, Song X, Jacobson RH, Takada S.
    Mol Cell Biol; 2007 Mar 07; 27(5):1844-58. PubMed ID: 17210644
    [Abstract] [Full Text] [Related]

  • 30. 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 07; 22(9):3178-93. PubMed ID: 11940675
    [Abstract] [Full Text] [Related]

  • 31. Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.
    Govind CK, Yoon S, Qiu H, Govind S, Hinnebusch AG.
    Mol Cell Biol; 2005 Jul 07; 25(13):5626-38. PubMed ID: 15964818
    [Abstract] [Full Text] [Related]

  • 32. Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo.
    Bhaumik SR, Green MR.
    Mol Cell Biol; 2002 Nov 07; 22(21):7365-71. PubMed ID: 12370284
    [Abstract] [Full Text] [Related]

  • 33. A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae.
    Huisinga KL, Pugh BF.
    Mol Cell; 2004 Feb 27; 13(4):573-85. PubMed ID: 14992726
    [Abstract] [Full Text] [Related]

  • 34. Architecture of the multi-functional SAGA complex and the molecular mechanism of holding TBP.
    Ben-Shem A, Papai G, Schultz P.
    FEBS J; 2021 May 27; 288(10):3135-3147. PubMed ID: 32946670
    [Abstract] [Full Text] [Related]

  • 35. Mot1 associates with transcriptionally active promoters and inhibits association of NC2 in Saccharomyces cerevisiae.
    Geisberg JV, Moqtaderi Z, Kuras L, Struhl K.
    Mol Cell Biol; 2002 Dec 27; 22(23):8122-34. PubMed ID: 12417716
    [Abstract] [Full Text] [Related]

  • 36. Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA.
    Donczew R, Warfield L, Pacheco D, Erijman A, Hahn S.
    Elife; 2020 Jan 08; 9():. PubMed ID: 31913117
    [Abstract] [Full Text] [Related]

  • 37. Taspase1 processing alters TFIIA cofactor properties in the regulation of TFIID.
    Malecová B, Caputo VS, Lee DF, Hsieh JJ, Oelgeschläger T.
    Transcription; 2015 Jan 08; 6(2):21-32. PubMed ID: 25996597
    [Abstract] [Full Text] [Related]

  • 38. TATA-binding protein-associated factor(s) in TFIID function through the initiator to direct basal transcription from a TATA-less class II promoter.
    Martinez E, Chiang CM, Ge H, Roeder RG.
    EMBO J; 1994 Jul 01; 13(13):3115-26. PubMed ID: 7518774
    [Abstract] [Full Text] [Related]

  • 39. Structure of SAGA and mechanism of TBP deposition on gene promoters.
    Papai G, Frechard A, Kolesnikova O, Crucifix C, Schultz P, Ben-Shem A.
    Nature; 2020 Jan 01; 577(7792):711-716. PubMed ID: 31969704
    [Abstract] [Full Text] [Related]

  • 40.
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