(Q24336865)

GOA release 2020-03-11

MRF binding

1 reference

Journal of Biological Chemistry

GOA release 2020-03-11

A Felsani

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G Condorelli

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A Giordano

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author name string

W Yuan

series ordinal

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M Caruso

series ordinal

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language of work or name

English

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publication date

12 April 1996

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published in

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volume

271

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issue

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page(s)

9009-13

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cites work

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Interaction of myogenic factors and the retinoblastoma protein mediates muscle cell commitment and differentiation

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Drosophila TAFII40 interacts with both a VP16 activation domain and the basal transcription factor TFIIB.

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E1A-associated p300 and CREB-associated CBP belong to a conserved family of coactivators

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Regulatory mechanisms that coordinate skeletal muscle differentiation and cell cycle withdrawal.

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Eukaryotic coactivators associated with the TATA box binding protein

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DNA tumor virus transforming proteins and the cell cycle

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Adenovirus E1A products suppress myogenic differentiation and inhibit transcription from muscle-specific promoters

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Interaction between an acidic activator and transcription factor TFIIB is required for transcriptional activation

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Phosphorylated CREB binds specifically to the nuclear protein CBP

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Nuclear protein CBP is a coactivator for the transcription factor CREB

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A family of transcriptional adaptor proteins targeted by the E1A oncoprotein

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Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP

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MyoD binds cooperatively to two sites in a target enhancer sequence: occupancy of two sites is required for activation

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Involvement of the cell-cycle inhibitor Cip1/WAF1 and the E1A-associated p300 protein in terminal differentiation.

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Ability of adenovirus 5 E1A proteins to suppress differentiation of BC3H1 myoblasts correlates with their binding to a 300 kDa cellular protein

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Multiple functional domains of human transcription factor IIB: distinct interactions with two general transcription factors and RNA polymerase II.

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bHLH factors in muscle development: dead lines and commitments, what to leave in and what to leave out

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Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor

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Relief of YY1 transcriptional repression by adenovirus E1A is mediated by E1A-associated protein p300

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Presence of a potent transcription activating sequence in the p53 protein

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Correlation of terminal cell cycle arrest of skeletal muscle with induction of p21 by MyoD.

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p53-independent expression of p21Cip1 in muscle and other terminally differentiating cells

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Analysis with specific polyclonal antiserum indicates that the E1A-associated 300-kDa product is a stable nuclear phosphoprotein that undergoes cell cycle phase-specific modification

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E1A-mediated inhibition of myogenesis correlates with a direct physical interaction of E1A12S and basic helix-loop-helix proteins

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