Methyl CpG binding proteins: coupling chromatin architecture to gene regulation (Q30654814)

26 June 2017

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title

Methyl CpG binding proteins: coupling chromatin architecture to gene regulation (English)

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26 June 2017

Wade PA

1

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PubMed ID

11420733

26 June 2017

language of work or name

English

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publication date

1 May 2001

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26 June 2017

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26 June 2017

20

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26 June 2017

3166-3173

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26 June 2017

24

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

26 June 2017

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Somatic frameshift mutations in the MBD4 gene of sporadic colon cancers with mismatch repair deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

The DNA methyltransferases of mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

A mammalian protein with specific demethylase activity for mCpG DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

MECP2 mutations account for most cases of typical forms of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Methylation-induced repression--belts, braces, and chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

The minimal repression domain of MBD2b overlaps with the methyl-CpG-binding domain and binds directly to Sin3A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Chromatin structure is required to block transcription of the methylated herpes simplex virus thymidine kinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

21 January 2018

CpG islands and genes

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Rett syndrome: a surprising result of mutation in MECP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

DNA recognition by the methyl-CpG binding domain of MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Methylation-mediated transcriptional silencing in euchromatin by methyl-CpG binding protein MBD1 isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Mutations in the MECP2 gene in a cohort of girls with Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Identification and characterization of a family of mammalian methyl-CpG binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

MeCP2 driven transcriptional repression in vitro: selectivity for methylated DNA, action at a distance and contacts with the basal transcription machinery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

DNA methylation directs a time-dependent repression of transcription initiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Novel de novo nonsense mutation of MECP2 in a patient with Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Active repression of methylated genes by the chromosomal protein MBD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Solution structure of the methyl-CpG-binding domain of the methylation-dependent transcriptional repressor MBD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

MECP2 mutation in male patients with non-specific X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Biphasic kinetics of the human DNA repair protein MED1 (MBD4), a mismatch-specific DNA N-glycosylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

CpG methylation, chromatin structure and gene silencing-a three-way connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

DNA methylation in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

The solution structure of the domain from MeCP2 that binds to methylated DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Mutation screening in Rett syndrome patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Functional consequences of Rett syndrome mutations on human MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

Mammalian methyltransferases and methyl-CpG-binding domains: proteins involved in DNA methylation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

Absence of genome-wide changes in DNA methylation during development of the zebrafish

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204340

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1204340

1 reference

PubMed ID

11420733

Dimensions Publication ID

26 June 2017

0 references

1 reference

PubMed ID

11420733