(Q24317494)

GOA release 2020-03-11

histone H2B acetylation

1 reference

GOA release 2020-03-11

author

Edison Liu

9

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Kinga Kamieniarz-Gdula

object named as

Kinga Kamieniarz-Gdula

4

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Marc Buehler

object named as

Marc Bühler

10

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Raphael Margueron

object named as

Raphael Margueron

11

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author name string

Philipp Tropberger

1

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Sebastian Pott

2

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Claudia Keller

3

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Matthieu Caron

5

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Florian Richter

6

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Guohong Li

7

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Gerhard Mittler

8

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Robert Schneider

Remodeling the chromatin structure of a nucleosome array by transcription factor-targeted trans-displacement of histones.

12

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language of work or name

English

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publication date

14 February 2013

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published in

Cell

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volume

152

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page(s)

859-72

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issue

4

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cites work

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E2A proteins enhance the histone acetyltransferase activity of the transcriptional co-activators CBP and p300

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spFRET using alternating excitation and FCS reveals progressive DNA unwrapping in nucleosomes

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Charge state of the globular histone core controls stability of the nucleosome

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Ordered cooperative functions of PRMT1, p300, and CARM1 in transcriptional activation by p53

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Chromatin modifications and their function

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A method for genetically installing site-specific acetylation in recombinant histones defines the effects of H3 K56 acetylation

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Preparation of nucleosome core particle from recombinant histones

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ACF, an ISWI-containing and ATP-utilizing chromatin assembly and remodeling factor

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Selective requirements for histone H3 and H4 N termini in p300-dependent transcriptional activation from chromatin.

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

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Regulation of chromatin by histone modifications

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Oncogenesis by sequestration of CBP/p300 in transcriptionally inactive hyperacetylated chromatin domains

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Distinct roles of GCN5/PCAF-mediated H3K9ac and CBP/p300-mediated H3K18/27ac in nuclear receptor transactivation

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Integrative model of genomic factors for determining binding site selection by estrogen receptor-α

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ChIP-seq accurately predicts tissue-specific activity of enhancers

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An oestrogen-receptor-α-bound human chromatin interactome

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Widespread transcription at neuronal activity-regulated enhancers

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A unique chromatin signature uncovers early developmental enhancers in humans

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Reprogramming transcription by distinct classes of enhancers functionally defined by eRNA

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Differential oestrogen receptor binding is associated with clinical outcome in breast cancer

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Genome-wide analysis of estrogen receptor binding sites

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Nucleosome dynamics define transcriptional enhancers

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Nucleosome eviction and activated transcription require p300 acetylation of histone H3 lysine 14.

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Histone H3K27ac separates active from poised enhancers and predicts developmental state

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Overlapping but distinct patterns of histone acetylation by the human coactivators p300 and PCAF within nucleosomal substrates

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Histone acetylation facilitates RNA polymerase II transcription of the Drosophila hsp26 gene in chromatin.

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

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Histone acetyltransferases regulate HIV-1 enhancer activity in vitro

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p300 and estrogen receptor cooperatively activate transcription via differential enhancement of initiation and reinitiation

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Nucleosome stability mediated by histone variants H3.3 and H2A.Z.

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Mediator coordinates PIC assembly with recruitment of CHD1

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Acetylation of H2A.Z is a key epigenetic modification associated with gene deregulation and epigenetic remodeling in cancer

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Nucleosome core displacement in vitro via a metastable transcription factor-nucleosome complex

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

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Binding of TATA binding protein to a naturally positioned nucleosome is facilitated by histone acetylation

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Methylation of histone H3 by Set2 in Saccharomyces cerevisiae is linked to transcriptional elongation by RNA polymerase II

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Insights into the role of histone H3 and histone H4 core modifiable residues in Saccharomyces cerevisiae

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Methylation of H2AR29 is a novel repressive PRMT6 target

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Mass spectrometric analysis of histone variants and post-translational modifications

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Oxidative burst and plant disease resistance

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Going global: novel histone modifications in the globular domain of H3

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