Covalent modifications of histones: expression from chromatin templates (Q48018634)

7 February 2018

review article

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title

Covalent modifications of histones: expression from chromatin templates (English)

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7 February 2018

author name string

Davie JR

series ordinal

1

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7 February 2018

publication date

1 April 1998

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7 February 2018

Current Opinion in Genetics & Development

published in

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7 February 2018

volume

8

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7 February 2018

issue

2

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7 February 2018

page(s)

173-178

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7 February 2018

Nuclear matrix, dynamic histone acetylation and transcriptionally active chromatin

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Histones associated with non-nucleosomal rat ribosomal genes are acetylated while those bound to nucleosome-organized gene copies are not.

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Histones in transit: cytosolic histone complexes and diacetylation of H4 during nucleosome assembly in human cells

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An activity gel assay detects a single, catalytically active histone acetyltransferase subunit in Tetrahymena macronuclei

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The CBP co-activator is a histone acetyltransferase

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The transcriptional coactivators p300 and CBP are histone acetyltransferases

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The TAF(II)250 subunit of TFIID has histone acetyltransferase activity

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Steroid receptor coactivator-1 is a histone acetyltransferase

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Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300

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

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

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Histone acetyltransferase activity and interaction with ADA2 are critical for GCN5 function in vivo.

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Interaction and functional collaboration of p300 and C/EBPβ

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AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer

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TRAM-1, A Novel 160-kDa Thyroid Hormone Receptor Activator Molecule, Exhibits Distinct Properties from Steroid Receptor Coactivator-1

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Nuclear receptor coactivators

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Purification and postsynthetic modifications of Friend erythroleukemic cell high mobility group protein HMG-I.

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Activation of p53 Sequence-Specific DNA Binding by Acetylation of the p53 C-Terminal Domain

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Acetylation of general transcription factors by histone acetyltransferases

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A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p

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HDA1 and HDA3 are components of a yeast histone deacetylase (HDA) complex

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HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription

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Isolation and Characterization of cDNAs Corresponding to an Additional Member of the Human Histone Deacetylase Gene Family

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Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3

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Identification of maize histone deacetylase HD2 as an acidic nucleolar phosphoprotein

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Histone deacetylase activity is required for full transcriptional repression by mSin3A

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A Large Protein Complex Containing the Yeast Sin3p and Rpd3p Transcriptional Regulators

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Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression

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A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression

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Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression

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Corepressor SMRT binds the BTB/POZ repressing domain of the LAZ3/BCL6 oncoprotein

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Properties of chicken erythrocyte histone deacetylase associated with the nuclear matrix

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Components of the human SWI/SNF complex are enriched in active chromatin and are associated with the nuclear matrix.

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The osteocalcin gene: a model for multiple parameters of skeletal-specific transcriptional control

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Mitogen-stimulated phosphorylation of histone H3 is targeted to a small hyperacetylation-sensitive fraction

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7 January 2021

Relationship between methylation and acetylation of arginine-rich histones in cycling and arrested HeLa cells

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7 January 2021

10.1016/S0959-437X(98)80138-X

Identifiers

DOI

1 reference

7 February 2018

1 reference

7 February 2018