MeCP2 nuclear dynamics in live neurons results from low and high affinity chromatin interactions (Q83224338)

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27 April 2020

title

MeCP2 nuclear dynamics in live neurons results from low and high affinity chromatin interactions (English)

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27 April 2020

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2

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27 April 2020

Elitsa I Stoyanova

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27 April 2020

Robert Tjian

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27 April 2020

Nathaniel Heintz

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27 April 2020

6

Anjana Rao

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27 April 2020

author name string

Francesco M Piccolo

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27 April 2020

Peng Dong

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27 April 2020

Ching-Lung Hsu

4

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language of work or name

English

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publication date

23 December 2019

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27 April 2020

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27 April 2020

volume

8

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Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

27 April 2020

cites work

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12 December 2020

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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The A.T-DNA-binding domain of mammalian high mobility group I chromosomal proteins. A novel peptide motif for recognizing DNA structure

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Selective dendritic alterations in the cortex of Rett syndrome

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA

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Functional consequences of Rett syndrome mutations on human MeCP2.

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The Ski protein family is required for MeCP2-mediated transcriptional repression

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Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

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Multiple modes of interaction between the methylated DNA binding protein MeCP2 and chromatin.

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Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo

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12 December 2020

MeCP2, a key contributor to neurological disease, activates and represses transcription

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12 December 2020

Dynamic multiple-target tracing to probe spatiotemporal cartography of cell membranes

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12 December 2020

The nuclear DNA base 5-hydroxymethylcytosine is present in Purkinje neurons and the brain

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BSMAP: whole genome bisulfite sequence MAPping program

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Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

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Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

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12 December 2020

Unique physical properties and interactions of the domains of methylated DNA binding protein 2.

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MeCP2 binds cooperatively to its substrate and competes with histone H1 for chromatin binding sites

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Tissue distribution of 5-hydroxymethylcytosine and search for active demethylation intermediates

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MeCP2 Rett mutations affect large scale chromatin organization.

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Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment

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MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system.

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An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders

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Methylation-dependent and -independent genomic targeting principles of the MBD protein family.

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Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor

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Global epigenomic reconfiguration during mammalian brain development

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Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome

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TNF and IL-1 exhibit distinct ubiquitin requirements for inducing NEMO-IKK supramolecular structures

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12 December 2020

Single-molecule dynamics of enhanceosome assembly in embryonic stem cells

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12 December 2020

Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice

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12 December 2020

Cell-type-specific repression by methyl-CpG-binding protein 2 is biased toward long genes

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12 December 2020

Lattice light-sheet microscopy: imaging molecules to embryos at high spatiotemporal resolution

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12 December 2020

Rett syndrome: a complex disorder with simple roots

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12 December 2020

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome

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A high-resolution imaging approach to investigate chromatin architecture in complex tissues

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The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome

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MECP2, a multi-talented modulator of chromatin architecture

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A dynamic mode of mitotic bookmarking by transcription factors

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Tet proteins influence the balance between neuroectodermal and mesodermal fate choice by inhibiting Wnt signaling

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The intervening domain from MeCP2 enhances the DNA affinity of the methyl binding domain and provides an independent DNA interaction site.

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Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders

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Live-cell p53 single-molecule binding is modulated by C-terminal acetylation and correlates with transcriptional activity.

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5-hydroxymethylcytosine accumulation in postmitotic neurons results in functional demethylation of expressed genes.

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Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.

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12 December 2020

Early-Life Gene Expression in Neurons Modulates Lasting Epigenetic States

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12 December 2020

Biophysical characterization of the basic cluster in the transcription repression domain of human MeCP2 with AT-rich DNA.

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12 December 2020

Robust model-based analysis of single-particle tracking experiments with Spot-On.

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12 December 2020

Visualizing transcription factor dynamics in living cells.

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12 December 2020

MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro.

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12 December 2020

Imaging dynamic and selective low-complexity domain interactions that control gene transcription

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12 December 2020

Species and cell-type properties of classically defined human and rodent neurons and glia

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12 December 2020

Identifiers

DOI

10.7554/ELIFE.51449

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31868585%20AND%20SRC:MED&resulttype=core&format=json

27 April 2020

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27 April 2020

PubMed publication ID

31868585

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