Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center. - Wikidata - wikimedia - TriplyDB

Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.

Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.

http://www.wikidata.org/entity/Q30310519

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In vitro and in vivo analyses of a Phe/Tyr switch controlling product specificity of histone lysine methyltransferases SALL3 interacts with DNMT3A and shows the ability to inhibit CpG island methylation in hepatocellular carcinoma Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome The odyssey of MeCP2 and parental imprinting Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication Functional analysis of the N- and C-terminus of mammalian G9a histone H3 methyltransferase The SET-domain protein superfamily: protein lysine methyltransferases MPP8 mediates the interactions between DNA methyltransferase Dnmt3a and H3K9 methyltransferase GLP/G9a Transcriptional gene silencing through epigenetic changes mediated by non-coding RNAs Antagonism between DNA and H3K27 methylation at the imprinted Rasgrf1 locus Histone H3-K9 methyltransferase ESET is essential for early development G9a/GLP complexes independently mediate H3K9 and DNA methylation to silence transcription Genome-wide and locus-specific DNA hypomethylation in G9a deficient mouse embryonic stem cells Diverse histone modifications on histone 3 lysine 9 and their relation to DNA methylation in specifying gene silencing.Coordinated chromatin control: structural and functional linkage of DNA and histone methylation.Involvement of histone H3 lysine 9 (H3K9) methyltransferase G9a in the maintenance of HIV-1 latency and its reactivation by BIX01294.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.Interaction of perinatal and pre-pubertal factors with genetic predisposition in the development of neural pathways involved in the regulation of energy homeostasis Developmental gene x environment interactions affecting systems regulating energy homeostasis and obesity.Domain-specific response of imprinted genes to reduced DNMT1.H3 lysine 9 methylation is maintained on a transcribed inverted repeat by combined action of SUVH6 and SUVH4 methyltransferases.Differential histone H3 Lys-9 and Lys-27 methylation profiles on the X chromosome.Epigenetic control of the genome-lessons from genomic imprinting Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.Dynamic patterns of histone lysine methylation in the developing retina.Palate morphogenesis: current understanding and future directions.A histone methylation-dependent DNA methylation pathway is uniquely impaired by deficiency in Arabidopsis S-adenosylhomocysteine hydrolase.Functional cooperation between HP1 and DNMT1 mediates gene silencing.Epigenetic regulation of retinal development and disease.Histone modifying and chromatin remodelling enzymes in cancer and dysplastic syndromes.Effect of BIX-01294 on H3K9me2 levels and the imprinted gene Snrpn in mouse embryonic fibroblast cells.Maintenance and regulation of DNA methylation patterns in mammals.Mechanism of mouse germ cell specification: a genetic program regulating epigenetic reprogramming.Automethylation of G9a and its implication in wider substrate specificity and HP1 binding.G9a histone methyltransferase contributes to imprinting in the mouse placenta.How imprinting centres work.EHMT2 directs DNA methylation for efficient gene silencing in mouse embryos.New insights into human pre-implantation metabolism in vivo and in vitro.G9a/GLP Complex Maintains Imprinted DNA Methylation in Embryonic Stem Cells

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P2860

Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.

http://www.wikidata.org/entity/Q30310519

description

2003 nî lūn-bûn

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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2003 թվականի փետրվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Role of histone methyltransfer ...... li syndrome imprinting center.

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Role of histone methyltransfer ...... li syndrome imprinting center.

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type

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Role of histone methyltransfer ...... li syndrome imprinting center.

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Role of histone methyltransfer ...... li syndrome imprinting center.

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Journal of Biological Chemistry

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Role of histone methyltransfer ...... li syndrome imprinting center.

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P2093

Edith Heard

http://www.w3.org/2001/XMLSchema#string

Joseph Wagstaff

http://www.w3.org/2001/XMLSchema#string

Makoto Tachibana

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Michele Guggiari

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Yoichi Shinkai

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Zhenghan Xin

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P2860

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

Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

High sensitivity mapping of methylated cytosines

G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis

Set domain-containing protein, G9a, is a novel lysine-preferring mammalian histone methyltransferase with hyperactivity and specific selectivity to lysines 9 and 27 of histone H3

A mouse model for Prader-Willi syndrome imprinting-centre mutations

Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center.

Control of CpNpG DNA methylation by the KRYPTONITE histone H3 methyltransferase

Role for DNA methylation in genomic imprinting

In vivo cross-linking and immunoprecipitation for studying dynamic Protein:DNA associations in a chromatin environment.

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14996-15000

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scholarly article

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10.1074/JBC.M211753200

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17

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278

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