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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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


Purification and functional characterization of SET8, a nucleosomal histone H4-lysine 20-specific methyltransferase.

Fang J, Feng Q, Ketel CS, Wang H, Cao R, Xia L, Erdjument-Bromage H, Tempst P, Simon JA, Zhang Y.

Curr Biol. 2002 Jul 9;12(13):1086-99.


In vivo effects of histone H3 depletion on nucleosome occupancy and position in Saccharomyces cerevisiae.

Gossett AJ, Lieb JD.

PLoS Genet. 2012;8(6):e1002771. doi: 10.1371/journal.pgen.1002771. Epub 2012 Jun 21.


Amino acid substitutions in the structured domains of histones H3 and H4 partially relieve the requirement of the yeast SWI/SNF complex for transcription.

Kruger W, Peterson CL, Sil A, Coburn C, Arents G, Moudrianakis EN, Herskowitz I.

Genes Dev. 1995 Nov 15;9(22):2770-9.


Compensatory interactions between Sir3p and the nucleosomal LRS surface imply their direct interaction.

Norris A, Bianchet MA, Boeke JD.

PLoS Genet. 2008 Dec;4(12):e1000301. doi: 10.1371/journal.pgen.1000301. Epub 2008 Dec 12.


Regulation of NuA4 histone acetyltransferase activity in transcription and DNA repair by phosphorylation of histone H4.

Utley RT, Lacoste N, Jobin-Robitaille O, Allard S, Côté J.

Mol Cell Biol. 2005 Sep;25(18):8179-90.


Sin mutations of histone H3: influence on nucleosome core structure and function.

Kurumizaka H, Wolffe AP.

Mol Cell Biol. 1997 Dec;17(12):6953-69.

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