411 related articles for article (PubMed ID: 15767675)
1. Promoter occupancy is a major determinant of chromatin remodeling enzyme requirements.
Dhasarathy A; Kladde MP
Mol Cell Biol; 2005 Apr; 25(7):2698-707. PubMed ID: 15767675
[TBL] [Abstract][Full Text] [Related]
2. Chromatin disassembly from the PHO5 promoter is essential for the recruitment of the general transcription machinery and coactivators.
Adkins MW; Williams SK; Linger J; Tyler JK
Mol Cell Biol; 2007 Sep; 27(18):6372-82. PubMed ID: 17620413
[TBL] [Abstract][Full Text] [Related]
3. Recruitment of the NuA4 complex poises the PHO5 promoter for chromatin remodeling and activation.
Nourani A; Utley RT; Allard S; Côté J
EMBO J; 2004 Jul; 23(13):2597-607. PubMed ID: 15175650
[TBL] [Abstract][Full Text] [Related]
4. Increasing the rate of chromatin remodeling and gene activation--a novel role for the histone acetyltransferase Gcn5.
Barbaric S; Walker J; Schmid A; Svejstrup JQ; Hörz W
EMBO J; 2001 Sep; 20(17):4944-51. PubMed ID: 11532958
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Polyphosphate loss promotes SNF/SWI- and Gcn5-dependent mitotic induction of PHO5.
Neef DW; Kladde MP
Mol Cell Biol; 2003 Jun; 23(11):3788-97. PubMed ID: 12748282
[TBL] [Abstract][Full Text] [Related]
7. Chromatin remodelling at the PHO8 promoter requires SWI-SNF and SAGA at a step subsequent to activator binding.
Gregory PD; Schmid A; Zavari M; Münsterkötter M; Hörz W
EMBO J; 1999 Nov; 18(22):6407-14. PubMed ID: 10562552
[TBL] [Abstract][Full Text] [Related]
8. Global role for chromatin remodeling enzymes in mitotic gene expression.
Krebs JE; Fry CJ; Samuels ML; Peterson CL
Cell; 2000 Sep; 102(5):587-98. PubMed ID: 11007477
[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. GCN5 dependence of chromatin remodeling and transcriptional activation by the GAL4 and VP16 activation domains in budding yeast.
Stafford GA; Morse RH
Mol Cell Biol; 2001 Jul; 21(14):4568-78. PubMed ID: 11416135
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.
Sudarsanam P; Cao Y; Wu L; Laurent BC; Winston F
EMBO J; 1999 Jun; 18(11):3101-6. PubMed ID: 10357821
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Evidence that Swi/Snf directly represses transcription in S. cerevisiae.
Martens JA; Winston F
Genes Dev; 2002 Sep; 16(17):2231-6. PubMed ID: 12208846
[TBL] [Abstract][Full Text] [Related]
15. An in vitro system recapitulates chromatin remodeling at the PHO5 promoter.
Haswell ES; O'Shea EK
Mol Cell Biol; 1999 Apr; 19(4):2817-27. PubMed ID: 10082547
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Targeting of Swi/Snf to the yeast GAL1 UAS G requires the Mediator, TAF IIs, and RNA polymerase II.
Lemieux K; Gaudreau L
EMBO J; 2004 Oct; 23(20):4040-50. PubMed ID: 15385957
[TBL] [Abstract][Full Text] [Related]
18. Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression.
Pollard KJ; Peterson CL
Mol Cell Biol; 1997 Nov; 17(11):6212-22. PubMed ID: 9343382
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Continuous and widespread roles for the Swi-Snf complex in transcription.
Biggar SR; Crabtree GR
EMBO J; 1999 Apr; 18(8):2254-64. PubMed ID: 10205178
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
