ATRX in chromatin assembly and genome architecture during development and disease. (Q50790126)

19 March 2018

title

ATRX in chromatin assembly and genome architecture during development and disease. (English)

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19 March 2018

author name string

Nathalie G Bérubé

series ordinal

1

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19 March 2018

publication date

18 August 2011

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Biochemistry and Cell Biology

published in

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volume

89

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issue

5

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page(s)

435-444

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Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family

cites work

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Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules

21 January 2018

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

21 January 2018

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Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome

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The chromatin remodelling factor dATRX is involved in heterochromatin formation

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ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells

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Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia

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Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo

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Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

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Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.

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Patient mutations alter ATRX targeting to PML nuclear bodies.

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A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD.

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Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein

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ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein

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Identification of differentially expressed genes in prostatic epithelium in relation to androgen receptor CAG repeat length.

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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

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The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9

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On the molecular etiology of Cornelia de Lange syndrome

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The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3

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Protein complex of Drosophila ATRX/XNP and HP1a is required for the formation of pericentric beta-heterochromatin in vivo

21 January 2018

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A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

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The H19 locus: role of an imprinted non-coding RNA in growth and development.

21 January 2018

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A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain

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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues

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ATRX: taming tandem repeats.

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

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

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

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Heterochromatin revisited

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RNA Polymerase II Is Required for RNAi-Dependent Heterochromatin Assembly

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ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain

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Epigenetic regulation of mammalian pericentric heterochromatin in vivo by HP1.

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ATP-dependent chromatin remodeling by the Saccharomyces cerevisiae homologous recombination factor Rdh54.

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

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

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Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

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The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome

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

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SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution

21 January 2018

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

21 January 2018

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Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome

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Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

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ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

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Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains

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Loss of ATRX leads to chromosome cohesion and congression defects

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Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development

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The XNP remodeler targets dynamic chromatin in Drosophila

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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.

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Aberrant calcium/calmodulin-dependent protein kinase II (CaMKII) activity is associated with abnormal dendritic spine morphology in the ATRX mutant mouse brain.

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Loss of ATRX in chondrocytes has minimal effects on skeletal development

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Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations

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Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair.

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A family-based study of the IL3RA gene on susceptibility to schizophrenia in a Chinese Han population

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A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein

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Regulation of imprinting in clusters: noncoding RNAs versus insulators

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Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence?

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Cohesin mediates transcriptional insulation by CCCTC-binding factor

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

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Cloning, expression and chromosome locations of the human DNMT3 gene family

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

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Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions.

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Separase-mediated cleavage of cohesin at interphase is required for DNA repair

21 January 2018

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21 January 2018

Identifiers

DOI

10.1139/O11-038

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19 March 2018

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19 March 2018