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Journal Abstract Search

339 related items for PubMed ID: 18682387

  • 1. Dissection of coactivator requirement at RNR3 reveals unexpected contributions from TFIID and SAGA.
    Zhang H, Kruk JA, Reese JC.
    J Biol Chem; 2008 Oct 10; 283(41):27360-27368. PubMed ID: 18682387
    [Abstract] [Full Text] [Related]

  • 2. SAGA Is a General Cofactor for RNA Polymerase II Transcription.
    Baptista T, Grünberg S, Minoungou N, Koster MJE, Timmers HTM, Hahn S, Devys D, Tora L.
    Mol Cell; 2017 Oct 05; 68(1):130-143.e5. PubMed ID: 28918903
    [Abstract] [Full Text] [Related]

  • 3. Exposing the core promoter is sufficient to activate transcription and alter coactivator requirement at RNR3.
    Zhang H, Reese JC.
    Proc Natl Acad Sci U S A; 2007 May 22; 104(21):8833-8. PubMed ID: 17502614
    [Abstract] [Full Text] [Related]

  • 4. SAGA mediates transcription from the TATA-like element independently of Taf1p/TFIID but dependent on core promoter structures in Saccharomyces cerevisiae.
    Watanabe K, Kokubo T.
    PLoS One; 2017 May 22; 12(11):e0188435. PubMed ID: 29176831
    [Abstract] [Full Text] [Related]

  • 5. The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.
    Saint M, Sawhney S, Sinha I, Singh RP, Dahiya R, Thakur A, Siddharthan R, Natarajan K.
    Mol Cell Biol; 2014 May 22; 34(9):1547-63. PubMed ID: 24550006
    [Abstract] [Full Text] [Related]

  • 6. 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 22; 577(7792):711-716. PubMed ID: 31969704
    [Abstract] [Full Text] [Related]

  • 7. SWI/SNF-dependent chromatin remodeling of RNR3 requires TAF(II)s and the general transcription machinery.
    Sharma VM, Li B, Reese JC.
    Genes Dev; 2003 Feb 15; 17(4):502-15. PubMed ID: 12600943
    [Abstract] [Full Text] [Related]

  • 8. Structure of the transcription coactivator SAGA.
    Wang H, Dienemann C, Stützer A, Urlaub H, Cheung ACM, Cramer P.
    Nature; 2020 Jan 15; 577(7792):717-720. PubMed ID: 31969703
    [Abstract] [Full Text] [Related]

  • 9. SAGA and TFIID: Friends of TBP drifting apart.
    Timmers HTM.
    Biochim Biophys Acta Gene Regul Mech; 2021 Feb 15; 1864(2):194604. PubMed ID: 32673655
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 25(13):5626-38. PubMed ID: 15964818
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A novel mechanism of antagonism between ATP-dependent chromatin remodeling complexes regulates RNR3 expression.
    Tomar RS, Psathas JN, Zhang H, Zhang Z, Reese JC.
    Mol Cell Biol; 2009 Jun 08; 29(12):3255-65. PubMed ID: 19349301
    [Abstract] [Full Text] [Related]

  • 13. Eaf1p Is Required for Recruitment of NuA4 in Targeting TFIID to the Promoters of the Ribosomal Protein Genes for Transcriptional Initiation In Vivo.
    Uprety B, Sen R, Bhaumik SR.
    Mol Cell Biol; 2015 Sep 01; 35(17):2947-64. PubMed ID: 26100014
    [Abstract] [Full Text] [Related]

  • 14. Transcriptional activation is weakened when Taf1p N-terminal domain 1 is substituted with its Drosophila counterpart in yeast TFIID.
    Kasahara K, Takahata S, Kokubo T.
    Genes Genet Syst; 2019 Apr 09; 94(1):51-59. PubMed ID: 30905891
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Sequential recruitment of SAGA and TFIID in a genomic response to DNA damage in Saccharomyces cerevisiae.
    Ghosh S, Pugh BF.
    Mol Cell Biol; 2011 Jan 05; 31(1):190-202. PubMed ID: 20956559
    [Abstract] [Full Text] [Related]

  • 17. An integrated SAGA and TFIID PIC assembly pathway selective for poised and induced promoters.
    Mittal C, Lang O, Lai WKM, Pugh BF.
    Genes Dev; 2022 Sep 01; 36(17-18):985-1001. PubMed ID: 36302553
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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]

  • 20. 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 27; 22(21):7365-71. PubMed ID: 12370284
    [Abstract] [Full Text] [Related]

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