Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin (Q27670415)

9

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Douglas Higgs

object named as

Douglas R Higgs

11

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author name string

Sebastian Eustermann

1

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Ji-Chun Yang

2

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Martin J Law

3

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Rachel Amos

4

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Lynda M Chapman

5

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Clare Jelinska

6

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David Garrick

7

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Daniela Rhodes

10

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David Neuhaus

Nature Structural & Molecular Biology

12

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publication date

12 June 2011

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published in

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volume

18

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page(s)

777-82

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issue

7

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cites work

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

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DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors

21 April 2017

1 reference

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

21 April 2017

1 reference

ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells

21 April 2017

1 reference

ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes

21 April 2017

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Distinct factors control histone variant H3.3 localization at specific genomic regions

21 April 2017

1 reference

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

21 April 2017

1 reference

Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres

21 April 2017

1 reference

The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain

21 April 2017

1 reference

Structural basis of HP1/PXVXL motif peptide interactions and HP1 localisation to heterochromatin

21 April 2017

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Structure of the HP1 chromodomain bound to histone H3 methylated at lysine 9

21 April 2017

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Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX

21 April 2017

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DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA

21 April 2017

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Structural basis for recognition of H3K4 methylation status by the DNA methyltransferase 3A ATRX-DNMT3-DNMT3L domain

21 April 2017

1 reference

Mechanism and regulation of acetylated histone binding by the tandem PHD finger of DPF3b

21 April 2017

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TRIM24 links a non-canonical histone signature to breast cancer

21 April 2017

1 reference

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

21 April 2017

1 reference

Heterochromatin formation in the mouse embryo requires critical residues of the histone variant H3.3

21 April 2017

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The Xplor-NIH NMR molecular structure determination package

21 April 2017

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The structure and biochemical properties of the human spliceosomal protein U1C

21 April 2017

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AQUA and PROCHECK-NMR: programs for checking the quality of protein structures solved by NMR

21 April 2017

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Regulation of HP1-chromatin binding by histone H3 methylation and phosphorylation

21 April 2017

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Loss of ATRX leads to chromosome cohesion and congression defects

21 April 2017

1 reference

ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.

21 January 2018

1 reference

Epigenetic regulation of mammalian pericentric heterochromatin in vivo by HP1.

21 January 2018

1 reference

Tethering of HP1 proteins to chromatin is relieved by phosphoacetylation of histone H3.

21 January 2018

1 reference

Interplay between DNA methylation, histone modification and chromatin remodeling in stem cells and during development

21 January 2018

1 reference

Chromodomain-mediated oligomerization of HP1 suggests a nucleosome-bridging mechanism for heterochromatin assembly.

21 January 2018

1 reference

Molecular-clinical spectrum of the ATR-X syndrome

21 January 2018

1 reference

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

31 March 2020

1 reference

Coordinate-based cluster analysis

31 March 2020

1 reference

31 March 2020

Identifiers

DOI

10.1038/NSMB.2070

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1693129

1047120165

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Fatcat ID

release_r6t57ji5dnchzbcnnt6g3sx3h4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/r6t57ji5dnchzbcnnt6g3sx3h4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1693129

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference