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Items: 1 to 20 of 401

1.

Differential contributions of histone H3 and H4 residues to heterochromatin structure.

Yu Q, Olsen L, Zhang X, Boeke JD, Bi X.

Genetics. 2011 Jun;188(2):291-308. doi: 10.1534/genetics.111.127886. Epub 2011 Mar 24.

2.

Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern.

Braunstein M, Sobel RE, Allis CD, Turner BM, Broach JR.

Mol Cell Biol. 1996 Aug;16(8):4349-56.

3.

A region of the nucleosome required for multiple types of transcriptional silencing in Saccharomyces cerevisiae.

Prescott ET, Safi A, Rusche LN.

Genetics. 2011 Jul;188(3):535-48. doi: 10.1534/genetics.111.129197. Epub 2011 May 5.

4.
5.

Silencing near tRNA genes is nucleosome-mediated and distinct from boundary element function.

Good PD, Kendall A, Ignatz-Hoover J, Miller EL, Pai DA, Rivera SR, Carrick B, Engelke DR.

Gene. 2013 Aug 15;526(1):7-15. doi: 10.1016/j.gene.2013.05.016. Epub 2013 May 23.

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9.

A core nucleosome surface crucial for transcriptional silencing.

Park JH, Cosgrove MS, Youngman E, Wolberger C, Boeke JD.

Nat Genet. 2002 Oct;32(2):273-9. Epub 2002 Sep 16.

PMID:
12244315
10.

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.

11.

The C-terminus of histone H2B is involved in chromatin compaction specifically at telomeres, independently of its monoubiquitylation at lysine 123.

Wang CY, Hua CY, Hsu HE, Hsu CL, Tseng HY, Wright DE, Hsu PH, Jen CH, Lin CY, Wu MY, Tsai MD, Kao CF.

PLoS One. 2011;6(7):e22209. doi: 10.1371/journal.pone.0022209. Epub 2011 Jul 29.

12.
13.

Identification of histone mutants that are defective for transcription-coupled nucleosome occupancy.

Hainer SJ, Martens JA.

Mol Cell Biol. 2011 Sep;31(17):3557-68. doi: 10.1128/MCB.05195-11. Epub 2011 Jul 5.

14.

Type B histone acetyltransferase Hat1p participates in telomeric silencing.

Kelly TJ, Qin S, Gottschling DE, Parthun MR.

Mol Cell Biol. 2000 Oct;20(19):7051-8.

15.

Histone H4 lysine 91 acetylation a core domain modification associated with chromatin assembly.

Ye J, Ai X, Eugeni EE, Zhang L, Carpenter LR, Jelinek MA, Freitas MA, Parthun MR.

Mol Cell. 2005 Apr 1;18(1):123-30.

16.

Comprehensive structural analysis of mutant nucleosomes containing lysine to glutamine (KQ) substitutions in the H3 and H4 histone-fold domains.

Iwasaki W, Tachiwana H, Kawaguchi K, Shibata T, Kagawa W, Kurumizaka H.

Biochemistry. 2011 Sep 13;50(36):7822-32. doi: 10.1021/bi201021h. Epub 2011 Aug 17.

PMID:
21812398
17.

Histone chaperone Rtt106 promotes nucleosome formation using (H3-H4)2 tetramers.

Fazly A, Li Q, Hu Q, Mer G, Horazdovsky B, Zhang Z.

J Biol Chem. 2012 Mar 30;287(14):10753-60. doi: 10.1074/jbc.M112.347450. Epub 2012 Feb 15.

18.

Centromere silencing and function in fission yeast is governed by the amino terminus of histone H3.

Mellone BG, Ball L, Suka N, Grunstein MR, Partridge JF, Allshire RC.

Curr Biol. 2003 Oct 14;13(20):1748-57.

19.

Interplay of chromatin modifiers on a short basic patch of histone H4 tail defines the boundary of telomeric heterochromatin.

Altaf M, Utley RT, Lacoste N, Tan S, Briggs SD, Côté J.

Mol Cell. 2007 Dec 28;28(6):1002-14.

20.

Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae.

Briggs SD, Bryk M, Strahl BD, Cheung WL, Davie JK, Dent SY, Winston F, Allis CD.

Genes Dev. 2001 Dec 15;15(24):3286-95.

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