Functional integration of the histone acetyltransferase MOF into the dosage compensation complex - Wikidata - wikimedia - TriplyDB

Functional integration of the histone acetyltransferase MOF into the dosage compensation complex

Functional integration of the histone acetyltransferase MOF into the dosage compensation complex

http://www.wikidata.org/entity/Q34348726

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Subunit composition and substrate specificity of a MOF-containing histone acetyltransferase distinct from the male-specific lethal (MSL) complex Metabolism, cytoskeleton and cellular signalling in the grip of protein Nepsilon - and O-acetylation Molecular architecture of quartet MOZ/MORF histone acetyltransferase complexes hMOF histone acetyltransferase is required for histone H4 lysine 16 acetylation in mammalian cells A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16 The MRG domain of human MRG15 uses a shallow hydrophobic pocket to interact with the N-terminal region of PAM14 Targeting determinants of dosage compensation in Drosophila The Functional Analysis of Histone Acetyltransferase MOF in Tumorigenesis Posttranscriptional control of X-chromosome dosage compensation Molecular Basis of the Interaction of Saccharomyces cerevisiae Eaf3 Chromo Domain with Methylated H3K36 Structural basis for MOF and MSL3 recruitment into the dosage compensation complex by MSL1 Solution Structure of MSL2 CXC Domain Reveals an Unusual Zn3Cys9 Cluster and Similarity to Pre-SET Domains of Histone Lysine Methyltransferases Structural insight into the regulation of MOF in the male-specific lethal complex and the non-specific lethal complex Crosstalk between NSL histone acetyltransferase and MLL/SET complexes: NSL complex functions in promoting histone H3K4 di-methylation activity by MLL/SET complexes Different chromatin interfaces of the Drosophila dosage compensation complex revealed by high-shear ChIP-seq.Site-specific acetylation of ISWI by GCN5.LTR retrotransposons and the evolution of dosage compensation in Drosophila.Risk of ovarian cancer and inherited variants in relapse-associated genes A new strategy for isolating genes controlling dosage compensation in Drosophila using a simple epigenetic mosaic eye phenotype Structure and function of histone acetyltransferase MOF Ubiquitylation of the acetyltransferase MOF in Drosophila melanogaster.Sex-biased transcription enhancement by a 5' tethered Gal4-MOF histone acetyltransferase fusion protein in Drosophila.The MRG domain mediates the functional integration of MSL3 into the dosage compensation complex.The DNA binding CXC domain of MSL2 is required for faithful targeting the Dosage Compensation Complex to the X chromosome The RING finger protein MSL2 in the MOF complex is an E3 ubiquitin ligase for H2B K34 and is involved in crosstalk with H3 K4 and K79 methylation Rapid purification of recombinant histones The amino-terminal region of Drosophila MSL1 contains basic, glycine-rich, and leucine zipper-like motifs that promote X chromosome binding, self-association, and MSL2 binding, respectively Dosage compensation and the global re-balancing of aneuploid genomes.Structural and biochemical studies on the chromo-barrel domain of male specific lethal 3 (MSL3) reveal a binding preference for mono- or dimethyllysine 20 on histone H4.Drosophila MOF controls Checkpoint protein2 and regulates genomic stability during early embryogenesis Structural basis of X chromosome DNA recognition by the MSL2 CXC domain during Drosophila dosage compensation.The Drosophila over compensating males gene genetically inhibits dosage compensation in males.Chromosome-wide gene-specific targeting of the Drosophila dosage compensation complex.X-chromosome targeting and dosage compensation are mediated by distinct domains in MSL-3.30 nm chromatin fibre decompaction requires both H4-K16 acetylation and linker histone eviction Role of the ATPase/helicase maleless (MLE) in the assembly, targeting, spreading and function of the male-specific lethal (MSL) complex of Drosophila.Deciphering the binding between Nupr1 and MSL1 and their DNA-repairing activity Modulations of hMOF autoacetylation by SIRT1 regulate hMOF recruitment and activities on the chromatin Dosage compensation in Drosophila.The right dose for every sex

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Functional integration of the histone acetyltransferase MOF into the dosage compensation complex

http://www.wikidata.org/entity/Q34348726

description

2004 nî lūn-bûn

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2004 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2004 թվականի մայիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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Functional integration of the ...... he dosage compensation complex

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Functional integration of the ...... he dosage compensation complex

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Functional integration of the ...... he dosage compensation complex

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Functional integration of the ...... he dosage compensation complex

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Functional integration of the ...... he dosage compensation complex

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Functional integration of the ...... he dosage compensation complex

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SJ.EMBOJ.7600235

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The EMBO Journal

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Functional integration of the ...... he dosage compensation complex

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Asifa Akhtar

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

Gabrielle Mengus

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Martin F Neumann

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Peter B Becker

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Tobias Straub

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Violette Morales

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P2860

Involvement of the TIP60 histone acetylase complex in DNA repair and apoptosis

The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substrate recognition.

A generic protein purification method for protein complex characterization and proteome exploration

The yeast NuA4 and Drosophila MSL complexes contain homologous subunits important for transcription regulation.

Sas4 and Sas5 are required for the histone acetyltransferase activity of Sas2 in the SAS complex.

Drosophila male-specific lethal-2 protein: structure/function analysis and dependence on MSL-1 for chromosome association.

The drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation

Guilt by association: non-coding RNAs, chromosome-specific proteins and dosage compensation in Drosophila.

The rox1 and rox2 RNAs are essential components of the compensasome, which mediates dosage compensation in Drosophila.

mof, a putative acetyl transferase gene related to the Tip60 and MOZ human genes and to the SAS genes of yeast, is required for dosage compensation in Drosophila.

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8565214

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15141166

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419912

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