(Q28204862)

Gene Ontology release 2020-05-02

M Merika

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D Thanos

series ordinal

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language of work or name

English

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publication date

April 2001

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published in

Current Opinion in Genetics & Development

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volume

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issue

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page(s)

205-8

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cites work

Modularity in promoters and enhancers

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Imposing specificity by localization: mechanism and evolvability

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Transcriptional activation: a complex puzzle with few easy pieces

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Gene Regulation for Higher Cells: A Theory

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Virus induction of human IFN beta gene expression requires the assembly of an enhanceosome

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Structure and function of the interferon-beta enhanceosome

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The IFN-beta enhancer: a paradigm for understanding activation and repression of inducible gene expression

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The high mobility group protein HMG I(Y) is required for NF-kappa B-dependent virus induction of the human IFN-beta gene

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Intra- and intermolecular cooperative binding of high-mobility-group protein I(Y) to the beta-interferon promoter

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Reversal of intrinsic DNA bends in the IFN beta gene enhancer by transcription factors and the architectural protein HMG I(Y)

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The role of HMG I(Y) in the assembly and function of the IFN-beta enhanceosome

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Upwardly mobile proteins. Workshop: the role of HMG proteins in chromatin structure, gene expression and neoplasia

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Acetylation of HMG I(Y) by CBP turns off IFN beta expression by disrupting the enhanceosome

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Mechanism for specificity by HMG-1 in enhanceosome assembly

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The nuclear factor-kappaB engages CBP/p300 and histone acetyltransferase activity for transcriptional activation of the interleukin-6 gene promoter.

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An enhanceosome containing the Jun B/Fra-2 heterodimer and the HMG-I(Y) architectural protein controls HPV 18 transcription

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Regulation of cell-type-specific interleukin-2 receptor alpha-chain gene expression: potential role of physical interactions between Elf-1, HMG-I(Y), and NF-kappa B family proteins

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Assembly and function of a TCR alpha enhancer complex is dependent on LEF-1-induced DNA bending and multiple protein-protein interactions

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TCRalpha enhancer activation occurs via a conformational change of a pre-assembled nucleo-protein complex

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Transcriptional coactivator, CIITA, is an acetyltransferase that bypasses a promoter requirement for TAF(II)250

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Stimulus-specific assembly of enhancer complexes on the tumor necrosis factor alpha gene promoter

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A lipopolysaccharide-specific enhancer complex involving Ets, Elk-1, Sp1, and CREB binding protein and p300 is recruited to the tumor necrosis factor alpha promoter in vivo

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Evidence for two modes of cooperative DNA binding in vivo that do not involve direct protein-protein interactions

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Ordered recruitment of chromatin modifying and general transcription factors to the IFN-beta promoter

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The mechanism of transcriptional synergy of an in vitro assembled interferon-beta enhanceosome

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Recruitment of CBP/p300 by the IFN beta enhanceosome is required for synergistic activation of transcription

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Efficient recruitment of TFIIB and CBP-RNA polymerase II holoenzyme by an interferon-beta enhanceosome in vitro

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Mechanism by which the IFN-beta enhanceosome activates transcription

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