256 related articles for article (PubMed ID: 12192044)
1. Targeted recruitment of Rpd3 histone deacetylase represses transcription by inhibiting recruitment of Swi/Snf, SAGA, and TATA binding protein.
Deckert J; Struhl K
Mol Cell Biol; 2002 Sep; 22(18):6458-70. PubMed ID: 12192044
[TBL] [Abstract][Full Text] [Related]
2. SWI/SNF binding to the HO promoter requires histone acetylation and stimulates TATA-binding protein recruitment.
Mitra D; Parnell EJ; Landon JW; Yu Y; Stillman DJ
Mol Cell Biol; 2006 Jun; 26(11):4095-110. PubMed ID: 16705163
[TBL] [Abstract][Full Text] [Related]
3. 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; 22(21):7365-71. PubMed ID: 12370284
[TBL] [Abstract][Full Text] [Related]
4. Mediator, TATA-binding protein, and RNA polymerase II contribute to low histone occupancy at active gene promoters in yeast.
Ansari SA; Paul E; Sommer S; Lieleg C; He Q; Daly AZ; Rode KA; Barber WT; Ellis LC; LaPorta E; Orzechowski AM; Taylor E; Reeb T; Wong J; Korber P; Morse RH
J Biol Chem; 2014 May; 289(21):14981-95. PubMed ID: 24727477
[TBL] [Abstract][Full Text] [Related]
5. Post-TATA binding protein recruitment clearance of Gcn5-dependent histone acetylation within promoter nucleosomes.
Topalidou I; Papamichos-Chronakis M; Thireos G
Mol Cell Biol; 2003 Nov; 23(21):7809-17. PubMed ID: 14560024
[TBL] [Abstract][Full Text] [Related]
6. Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p.
Qiu H; Hu C; Zhang F; Hwang GJ; Swanson MJ; Boonchird C; Hinnebusch AG
Mol Cell Biol; 2005 May; 25(9):3461-74. PubMed ID: 15831453
[TBL] [Abstract][Full Text] [Related]
7. Hyperacetylation of chromatin at the ADH2 promoter allows Adr1 to bind in repressed conditions.
Verdone L; Wu J; van Riper K; Kacherovsky N; Vogelauer M; Young ET; Grunstein M; Di Mauro E; Caserta M
EMBO J; 2002 Mar; 21(5):1101-11. PubMed ID: 11867538
[TBL] [Abstract][Full Text] [Related]
8. 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; 25(13):5626-38. PubMed ID: 15964818
[TBL] [Abstract][Full Text] [Related]
9. Role for Nhp6, Gcn5, and the Swi/Snf complex in stimulating formation of the TATA-binding protein-TFIIA-DNA complex.
Biswas D; Imbalzano AN; Eriksson P; Yu Y; Stillman DJ
Mol Cell Biol; 2004 Sep; 24(18):8312-21. PubMed ID: 15340090
[TBL] [Abstract][Full Text] [Related]
10. Targeted recruitment of the Sin3-Rpd3 histone deacetylase complex generates a highly localized domain of repressed chromatin in vivo.
Kadosh D; Struhl K
Mol Cell Biol; 1998 Sep; 18(9):5121-7. PubMed ID: 9710596
[TBL] [Abstract][Full Text] [Related]
11. Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium.
Ricci AR; Genereaux J; Brandl CJ
Mol Cell Biol; 2002 Jun; 22(12):4033-42. PubMed ID: 12024017
[TBL] [Abstract][Full Text] [Related]
12. Architectural transcription factors and the SAGA complex function in parallel pathways to activate transcription.
Yu Y; Eriksson P; Stillman DJ
Mol Cell Biol; 2000 Apr; 20(7):2350-7. PubMed ID: 10713159
[TBL] [Abstract][Full Text] [Related]
13. Function and selectivity of bromodomains in anchoring chromatin-modifying complexes to promoter nucleosomes.
Hassan AH; Prochasson P; Neely KE; Galasinski SC; Chandy M; Carrozza MJ; Workman JL
Cell; 2002 Nov; 111(3):369-79. PubMed ID: 12419247
[TBL] [Abstract][Full Text] [Related]
14. SAGA and Rpd3 chromatin modification complexes dynamically regulate heat shock gene structure and expression.
Kremer SB; Gross DS
J Biol Chem; 2009 Nov; 284(47):32914-31. PubMed ID: 19759026
[TBL] [Abstract][Full Text] [Related]
15. Histone acetyltransferase complexes stabilize swi/snf binding to promoter nucleosomes.
Hassan AH; Neely KE; Workman JL
Cell; 2001 Mar; 104(6):817-27. PubMed ID: 11290320
[TBL] [Abstract][Full Text] [Related]
16. Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters.
Kadosh D; Struhl K
Cell; 1997 May; 89(3):365-71. PubMed ID: 9150136
[TBL] [Abstract][Full Text] [Related]
17. 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; 17(4):502-15. PubMed ID: 12600943
[TBL] [Abstract][Full Text] [Related]
18. Regulation of TATA-binding protein binding by the SAGA complex and the Nhp6 high-mobility group protein.
Yu Y; Eriksson P; Bhoite LT; Stillman DJ
Mol Cell Biol; 2003 Mar; 23(6):1910-21. PubMed ID: 12612066
[TBL] [Abstract][Full Text] [Related]
19. The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4.
Larschan E; Winston F
Genes Dev; 2001 Aug; 15(15):1946-56. PubMed ID: 11485989
[TBL] [Abstract][Full Text] [Related]
20. Localized histone acetylation and deacetylation triggered by the homologous recombination pathway of double-strand DNA repair.
Tamburini BA; Tyler JK
Mol Cell Biol; 2005 Jun; 25(12):4903-13. PubMed ID: 15923609
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]