338 related articles for article (PubMed ID: 11967287)
1. Epstein-Barr virus nuclear antigen 3C and prothymosin alpha interact with the p300 transcriptional coactivator at the CH1 and CH3/HAT domains and cooperate in regulation of transcription and histone acetylation.
Subramanian C; Hasan S; Rowe M; Hottiger M; Orre R; Robertson ES
J Virol; 2002 May; 76(10):4699-708. PubMed ID: 11967287
[TBL] [Abstract][Full Text] [Related]
2. Modulation of histone acetyltransferase activity through interaction of epstein-barr nuclear antigen 3C with prothymosin alpha.
Cotter MA; Robertson ES
Mol Cell Biol; 2000 Aug; 20(15):5722-35. PubMed ID: 10891508
[TBL] [Abstract][Full Text] [Related]
3. Epstein-Barr virus nuclear antigen 3C recruits histone deacetylase activity and associates with the corepressors mSin3A and NCoR in human B-cell lines.
Knight JS; Lan K; Subramanian C; Robertson ES
J Virol; 2003 Apr; 77(7):4261-72. PubMed ID: 12634383
[TBL] [Abstract][Full Text] [Related]
4. Epstein-Barr virus nuclear protein 2 interacts with p300, CBP, and PCAF histone acetyltransferases in activation of the LMP1 promoter.
Wang L; Grossman SR; Kieff E
Proc Natl Acad Sci U S A; 2000 Jan; 97(1):430-5. PubMed ID: 10618435
[TBL] [Abstract][Full Text] [Related]
5. Stimulation of CREB binding protein nucleosomal histone acetyltransferase activity by a class of transcriptional activators.
Chen CJ; Deng Z; Kim AY; Blobel GA; Lieberman PM
Mol Cell Biol; 2001 Jan; 21(2):476-87. PubMed ID: 11134336
[TBL] [Abstract][Full Text] [Related]
6. Epstein-Barr Virus Nuclear Antigen 3C Inhibits Expression of
Gillman ACT; Parker G; Allday MJ; Bazot Q
J Virol; 2018 Nov; 92(21):. PubMed ID: 30135119
[TBL] [Abstract][Full Text] [Related]
7. Epstein-barr virus nuclear antigen 3C activates the latent membrane protein 1 promoter in the presence of Epstein-Barr virus nuclear antigen 2 through sequences encompassing an spi-1/Spi-B binding site.
Zhao B; Sample CE
J Virol; 2000 Jun; 74(11):5151-60. PubMed ID: 10799590
[TBL] [Abstract][Full Text] [Related]
8. Histone acetyltransferase activity of p300 is required for transcriptional repression by the promyelocytic leukemia zinc finger protein.
Guidez F; Howell L; Isalan M; Cebrat M; Alani RM; Ivins S; Hormaeche I; McConnell MJ; Pierce S; Cole PA; Licht J; Zelent A
Mol Cell Biol; 2005 Jul; 25(13):5552-66. PubMed ID: 15964811
[TBL] [Abstract][Full Text] [Related]
9. The CBP bromodomain and nucleosome targeting are required for Zta-directed nucleosome acetylation and transcription activation.
Deng Z; Chen CJ; Chamberlin M; Lu F; Blobel GA; Speicher D; Cirillo LA; Zaret KS; Lieberman PM
Mol Cell Biol; 2003 Apr; 23(8):2633-44. PubMed ID: 12665567
[TBL] [Abstract][Full Text] [Related]
10. Transcriptional activation by thyroid hormone receptor-beta involves chromatin remodeling, histone acetylation, and synergistic stimulation by p300 and steroid receptor coactivators.
Lee KC; Li J; Cole PA; Wong J; Kraus WL
Mol Endocrinol; 2003 May; 17(5):908-22. PubMed ID: 12586842
[TBL] [Abstract][Full Text] [Related]
11. Acetylation of nucleosomal histones by p300 facilitates transcription from tax-responsive human T-cell leukemia virus type 1 chromatin template.
Lu H; Pise-Masison CA; Fletcher TM; Schiltz RL; Nagaich AK; Radonovich M; Hager G; Cole PA; Brady JN
Mol Cell Biol; 2002 Jul; 22(13):4450-62. PubMed ID: 12052856
[TBL] [Abstract][Full Text] [Related]
12. Angiotensinogen gene expression is dependent on signal transducer and activator of transcription 3-mediated p300/cAMP response element binding protein-binding protein coactivator recruitment and histone acetyltransferase activity.
Ray S; Sherman CT; Lu M; Brasier AR
Mol Endocrinol; 2002 Apr; 16(4):824-36. PubMed ID: 11923478
[TBL] [Abstract][Full Text] [Related]
13. EBNA3C coactivation with EBNA2 requires a SUMO homology domain.
Rosendorff A; Illanes D; David G; Lin J; Kieff E; Johannsen E
J Virol; 2004 Jan; 78(1):367-77. PubMed ID: 14671118
[TBL] [Abstract][Full Text] [Related]
14. Acetylation by histone acetyltransferase CREB-binding protein/p300 of STAT6 is required for transcriptional activation of the 15-lipoxygenase-1 gene.
Shankaranarayanan P; Chaitidis P; Kühn H; Nigam S
J Biol Chem; 2001 Nov; 276(46):42753-60. PubMed ID: 11509556
[TBL] [Abstract][Full Text] [Related]
15. Coactivators p300 and PCAF physically and functionally interact with the foamy viral trans-activator.
Bannert H; Muranyi W; Ogryzko VV; Nakatani Y; Flügel RM
BMC Mol Biol; 2004 Sep; 5():16. PubMed ID: 15350211
[TBL] [Abstract][Full Text] [Related]
16. Akt phosphorylation of p300 at Ser-1834 is essential for its histone acetyltransferase and transcriptional activity.
Huang WC; Chen CC
Mol Cell Biol; 2005 Aug; 25(15):6592-602. PubMed ID: 16024795
[TBL] [Abstract][Full Text] [Related]
17. Transcriptional activators direct histone acetyltransferase complexes to nucleosomes.
Utley RT; Ikeda K; Grant PA; Côté J; Steger DJ; Eberharter A; John S; Workman JL
Nature; 1998 Jul; 394(6692):498-502. PubMed ID: 9697775
[TBL] [Abstract][Full Text] [Related]
18. Regulation of interaction of the acetyltransferase region of p300 and the DNA-binding domain of Sp1 on and through DNA binding.
Suzuki T; Kimura A; Nagai R; Horikoshi M
Genes Cells; 2000 Jan; 5(1):29-41. PubMed ID: 10651903
[TBL] [Abstract][Full Text] [Related]
19. P300/CBP acts as a coactivator to cartilage homeoprotein-1 (Cart1), paired-like homeoprotein, through acetylation of the conserved lysine residue adjacent to the homeodomain.
Iioka T; Furukawa K; Yamaguchi A; Shindo H; Yamashita S; Tsukazaki T
J Bone Miner Res; 2003 Aug; 18(8):1419-29. PubMed ID: 12929931
[TBL] [Abstract][Full Text] [Related]
20. Epstein-Barr virus nuclear antigen 3C is a powerful repressor of transcription when tethered to DNA.
Bain M; Watson RJ; Farrell PJ; Allday MJ
J Virol; 1996 Apr; 70(4):2481-9. PubMed ID: 8642676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
