312 related articles for article (PubMed ID: 12776737)
1. Stimulation of c-MYC transcriptional activity and acetylation by recruitment of the cofactor CBP.
Vervoorts J; Lüscher-Firzlaff JM; Rottmann S; Lilischkis R; Walsemann G; Dohmann K; Austen M; Lüscher B
EMBO Rep; 2003 May; 4(5):484-90. PubMed ID: 12776737
[TBL] [Abstract][Full Text] [Related]
2. Dual regulation of c-Myc by p300 via acetylation-dependent control of Myc protein turnover and coactivation of Myc-induced transcription.
Faiola F; Liu X; Lo S; Pan S; Zhang K; Lymar E; Farina A; Martinez E
Mol Cell Biol; 2005 Dec; 25(23):10220-34. PubMed ID: 16287840
[TBL] [Abstract][Full Text] [Related]
3. Acetylation-mediated transcriptional activation of the ETS protein ER81 by p300, P/CAF, and HER2/Neu.
Goel A; Janknecht R
Mol Cell Biol; 2003 Sep; 23(17):6243-54. PubMed ID: 12917345
[TBL] [Abstract][Full Text] [Related]
4. E2F transcriptional activation requires TRRAP and GCN5 cofactors.
Lang SE; McMahon SB; Cole MD; Hearing P
J Biol Chem; 2001 Aug; 276(35):32627-34. PubMed ID: 11418595
[TBL] [Abstract][Full Text] [Related]
5. Histone acetylation by p300 is involved in CREB-mediated transcription on chromatin.
Yuan LW; Gambee JE
Biochim Biophys Acta; 2001 Dec; 1541(3):161-9. PubMed ID: 11755210
[TBL] [Abstract][Full Text] [Related]
6. Interaction of EVI1 with cAMP-responsive element-binding protein-binding protein (CBP) and p300/CBP-associated factor (P/CAF) results in reversible acetylation of EVI1 and in co-localization in nuclear speckles.
Chakraborty S; Senyuk V; Sitailo S; Chi Y; Nucifora G
J Biol Chem; 2001 Nov; 276(48):44936-43. PubMed ID: 11568182
[TBL] [Abstract][Full Text] [Related]
7. The ATM-related domain of TRRAP is required for histone acetyltransferase recruitment and Myc-dependent oncogenesis.
Park J; Kunjibettu S; McMahon SB; Cole MD
Genes Dev; 2001 Jul; 15(13):1619-24. PubMed ID: 11445536
[TBL] [Abstract][Full Text] [Related]
8. MYC interacts with the human STAGA coactivator complex via multivalent contacts with the GCN5 and TRRAP subunits.
Zhang N; Ichikawa W; Faiola F; Lo SY; Liu X; Martinez E
Biochim Biophys Acta; 2014 May; 1839(5):395-405. PubMed ID: 24705139
[TBL] [Abstract][Full Text] [Related]
9. CREB-binding protein/p300 co-activation of crystallin gene expression.
Chen Q; Dowhan DH; Liang D; Moore DD; Overbeek PA
J Biol Chem; 2002 Jul; 277(27):24081-9. PubMed ID: 11943779
[TBL] [Abstract][Full Text] [Related]
10. Functional analysis of the p300 acetyltransferase domain: the PHD finger of p300 but not of CBP is dispensable for enzymatic activity.
Bordoli L; Hüsser S; Lüthi U; Netsch M; Osmani H; Eckner R
Nucleic Acids Res; 2001 Nov; 29(21):4462-71. PubMed ID: 11691934
[TBL] [Abstract][Full Text] [Related]
11. Ataxin-3 is a histone-binding protein with two independent transcriptional corepressor activities.
Li F; Macfarlan T; Pittman RN; Chakravarti D
J Biol Chem; 2002 Nov; 277(47):45004-12. PubMed ID: 12297501
[TBL] [Abstract][Full Text] [Related]
12. The essential cofactor TRRAP recruits the histone acetyltransferase hGCN5 to c-Myc.
McMahon SB; Wood MA; Cole MD
Mol Cell Biol; 2000 Jan; 20(2):556-62. PubMed ID: 10611234
[TBL] [Abstract][Full Text] [Related]
13. The histone acetyltransferase activity of PCAF cooperates with the brahma/SWI2-related protein BRG-1 in the activation of the enhancer A of the MHC class I promoter.
Brockmann D; Lehmkühler O; Schmücker U; Esche H
Gene; 2001 Oct; 277(1-2):111-20. PubMed ID: 11602348
[TBL] [Abstract][Full Text] [Related]
14. c-Myc transformation domain recruits the human STAGA complex and requires TRRAP and GCN5 acetylase activity for transcription activation.
Liu X; Tesfai J; Evrard YA; Dent SY; Martinez E
J Biol Chem; 2003 May; 278(22):20405-12. PubMed ID: 12660246
[TBL] [Abstract][Full Text] [Related]
15. The c-MYC oncoprotein is a substrate of the acetyltransferases hGCN5/PCAF and TIP60.
Patel JH; Du Y; Ard PG; Phillips C; Carella B; Chen CJ; Rakowski C; Chatterjee C; Lieberman PM; Lane WS; Blobel GA; McMahon SB
Mol Cell Biol; 2004 Dec; 24(24):10826-34. PubMed ID: 15572685
[TBL] [Abstract][Full Text] [Related]
16. Developmentally regulated expression of the transcriptional cofactors/histone acetyltransferases CBP and p300 during mouse embryogenesis.
Partanen A; Motoyama J; Hui CC
Int J Dev Biol; 1999 Sep; 43(6):487-94. PubMed ID: 10610021
[TBL] [Abstract][Full Text] [Related]
17. TRRAP and GCN5 are used by c-Myc to activate RNA polymerase III transcription.
Kenneth NS; Ramsbottom BA; Gomez-Roman N; Marshall L; Cole PA; White RJ
Proc Natl Acad Sci U S A; 2007 Sep; 104(38):14917-22. PubMed ID: 17848523
[TBL] [Abstract][Full Text] [Related]
18. Lysine acetyltransferases cyclic adenosine monophosphate response element-binding binding protein and acetyltransferase p300 attenuate transcriptional activity of the mineralocorticoid receptor through its acetylation.
Seo M; Song M; Seok YM; Kang SH; Lee HA; Sohn UD; Kim IK
Clin Exp Pharmacol Physiol; 2015 May; 42(5):559-66. PubMed ID: 25707758
[TBL] [Abstract][Full Text] [Related]
19. Transcriptional regulation by p53 through intrinsic DNA/chromatin binding and site-directed cofactor recruitment.
Espinosa JM; Emerson BM
Mol Cell; 2001 Jul; 8(1):57-69. PubMed ID: 11511360
[TBL] [Abstract][Full Text] [Related]
20. p300 and p300/cAMP-response element-binding protein-associated factor acetylate the androgen receptor at sites governing hormone-dependent transactivation.
Fu M; Wang C; Reutens AT; Wang J; Angeletti RH; Siconolfi-Baez L; Ogryzko V; Avantaggiati ML; Pestell RG
J Biol Chem; 2000 Jul; 275(27):20853-60. PubMed ID: 10779504
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
