MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation (Q28210381)

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James K Leung

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John C Lucchesi

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Olivia M Pereira-Smith

Journal of Biological Chemistry

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language of work or name

English

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publication date

27 December 2002

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published in

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volume

277

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issue

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page(s)

50860-6

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cites work

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Mammalian chromodomain proteins: their role in genome organisation and expression

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Structure of the chromatin binding (chromo) domain from mouse modifier protein 1.

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Self-association of chromo domain peptides.

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Heterochromatin formation in mammalian cells: interaction between histones and HP1 proteins

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Chromodomains are protein-RNA interaction modules

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Origin and evolution of the regulatory gene male-specific lethal-3.

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Recycling to remodel: evolution of dosage-compensation complexes

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Conservation of the MORF4 related gene family: identification of a new chromo domain subfamily and novel protein motif

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Regulation of the sex-specific binding of the maleless dosage compensation protein to the male X chromosome in Drosophila.

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MRG15 activates the B-myb promoter through formation of a nuclear complex with the retinoblastoma protein and the novel protein PAM14

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A new human member of the MYST family of histone acetyl transferases with high sequence similarity to Drosophila MOF

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

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CCAAT/enhancer-binding protein alpha (C/EBP alpha) inhibits cell proliferation through the p21 (WAF-1/CIP-1/SDI-1) protein

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

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

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Constitutive expression of B-myb can bypass p53-induced Waf1/Cip1-mediated G1 arrest

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Regulation of BALB/c 3T3 fibroblast proliferation by B-myb is accompanied by selective activation of cdc2 and cyclin D1 expression

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Evidence for the recessive nature of cellular immortality

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Identifiers

DOI

10.1074/JBC.M203839200

1 reference

Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12397079

1 reference

Consolidated OpenCitations Corpus – April 2017