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Items: 1 to 20 of 416

1.
2.

Histone H3 specific acetyltransferases are essential for cell cycle progression.

Howe L, Auston D, Grant P, John S, Cook RG, Workman JL, Pillus L.

Genes Dev. 2001 Dec 1;15(23):3144-54.

3.

Transcription-linked acetylation by Gcn5p of histones H3 and H4 at specific lysines.

Kuo MH, Brownell JE, Sobel RE, Ranalli TA, Cook RG, Edmondson DG, Roth SY, Allis CD.

Nature. 1996 Sep 19;383(6597):269-72.

PMID:
8805705
4.

Phosphorylation of serine 10 in histone H3 is functionally linked in vitro and in vivo to Gcn5-mediated acetylation at lysine 14.

Lo WS, Trievel RC, Rojas JR, Duggan L, Hsu JY, Allis CD, Marmorstein R, Berger SL.

Mol Cell. 2000 Jun;5(6):917-26.

6.

Functional connection between histone acetyltransferase Gcn5p and methyltransferase Hmt1p.

Kuo MH, Xu XJ, Bolck HA, Guo D.

Biochim Biophys Acta. 2009 May;1789(5):395-402. doi: 10.1016/j.bbagrm.2009.03.004. Epub 2009 Apr 7.

7.

Acetylation of Rsc4p by Gcn5p is essential in the absence of histone H3 acetylation.

Choi JK, Grimes DE, Rowe KM, Howe LJ.

Mol Cell Biol. 2008 Dec;28(23):6967-72. doi: 10.1128/MCB.00570-08. Epub 2008 Sep 22.

8.

Gcn5p is involved in the acetylation of histone H3 in nucleosomes.

Ruiz-García AB, Sendra R, Pamblanco M, Tordera V.

FEBS Lett. 1997 Feb 17;403(2):186-90.

9.

NuA4 links methylation of histone H3 lysines 4 and 36 to acetylation of histones H4 and H3.

Ginsburg DS, Anlembom TE, Wang J, Patel SR, Li B, Hinnebusch AG.

J Biol Chem. 2014 Nov 21;289(47):32656-70. doi: 10.1074/jbc.M114.585588. Epub 2014 Oct 9.

10.

Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo.

Kuo MH, Zhou J, Jambeck P, Churchill ME, Allis CD.

Genes Dev. 1998 Mar 1;12(5):627-39.

11.

Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex.

Grant PA, Duggan L, Côté J, Roberts SM, Brownell JE, Candau R, Ohba R, Owen-Hughes T, Allis CD, Winston F, Berger SL, Workman JL.

Genes Dev. 1997 Jul 1;11(13):1640-50.

12.
14.

Site-specific loss of acetylation upon phosphorylation of histone H3.

Edmondson DG, Davie JK, Zhou J, Mirnikjoo B, Tatchell K, Dent SY.

J Biol Chem. 2002 Aug 16;277(33):29496-502. Epub 2002 May 30.

15.

Deposition-related sites K5/K12 in histone H4 are not required for nucleosome deposition in yeast.

Ma XJ, Wu J, Altheim BA, Schultz MC, Grunstein M.

Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6693-8.

16.

Histone acetyltransferase activity is conserved between yeast and human GCN5 and is required for complementation of growth and transcriptional activation.

Wang L, Mizzen C, Ying C, Candau R, Barlev N, Brownell J, Allis CD, Berger SL.

Mol Cell Biol. 1997 Jan;17(1):519-27.

17.

Expanded lysine acetylation specificity of Gcn5 in native complexes.

Grant PA, Eberharter A, John S, Cook RG, Turner BM, Workman JL.

J Biol Chem. 1999 Feb 26;274(9):5895-900.

19.

The Gcn5 bromodomain co-ordinates nucleosome remodelling.

Syntichaki P, Topalidou I, Thireos G.

Nature. 2000 Mar 23;404(6776):414-7.

PMID:
10746732
20.

Tandem bromodomains in the chromatin remodeler RSC recognize acetylated histone H3 Lys14.

Kasten M, Szerlong H, Erdjument-Bromage H, Tempst P, Werner M, Cairns BR.

EMBO J. 2004 Mar 24;23(6):1348-59. Epub 2004 Mar 4.

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