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C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300.

C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Research Abstract Details 

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  • C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Abstract Text:

    haitao wangHaitao Wang,brian larrisBrian Larris,t harshani peirisT Harshani Peiris,liping zhangLiping Zhang,john le layJohn Le Lay,yan gaoYan Gao,linda e greenbaumLinda E Greenbaum,

    The E2F transcription factors play an essential role in regulating the G(1)- to S-phase transition of the cell cycle. Previous studies have identified the importance of interactions between E2Fs and other transcription factors as a mechanism for transcriptional control of a subset of E2F regulated target genes. However, the mechanisms responsible for E2F target gene specificity remain incompletely understood. Here we report that in a mammalian in vivo model of synchronized proliferation, C/EBPbeta occupancy on the promoters of E2F-regulated growth-related genes increases as a function of cell cycle progression. C/EPBbeta binding to these promoters is associated with recruitment of the coactivator CBP/p300, histone H4 acetylation, and maximal activation of E2F target genes. Moreover, binding of CBP/p300 to E2F targets is markedly reduced in C/EBPbeta null mice, resulting in reduced expression of E2F regulated genes. These findings identify C/EBPbeta as a direct activator of E2F target genes in mammalian cell cycle progression through a mechanism that involves recruitment of CBP/p300. The demonstration of a functional link between C/EBPbeta and CBP/p300 for E2F target gene activation provides a potential mechanism for how coactivators such as CBP/p300 can be selectively recruited to E2F target genes in response to tissue-specific growth stimuli.

    C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Publishing Authors By Initials

    h wangH Wang,b larrisB Larris,th peirisTH Peiris,l zhangL Zhang,j le layJ Le Lay,y gaoY Gao,le greenbaumLE Greenbaum,

    For similar enzymes and coenzymes: enzymes: transferases: acyltransferases: acetyltransferases: p300-cbp transcription factors research abstracts see: enzymes and coenzymes: enzymes: transferases: acyltransferases: acetyltransferases: p300-cbp transcription factors research

    PUBMED ID PMID:

    MEDLINE DATE:

    C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: The Journal of biological chemistry

    VOLUME: 282

    Page Numbers: 24679-88

    Journal Abbreviation: J. Biol. Chem.

    ISSN: 0021-9258

    DAY: 27

    MONTH: 06

    YEAR: 2007

    C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 2985121

    C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Keywords Mesh Terms:

    KEYWORDS: p300-CBP Transcription Factors

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300. Information

    Substance Name: p300-CBP Transcription Factors

    Registry Number: EC 2.3.1.48

    Grant and Affiliation Information for C/EBPbeta activates E2F-regulated genes in vivo via recruitment of the coactivator CREB-binding protein/P300.

    AFFILIATION: Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: DK-056669

    ACRONYM: DK

    MEDLINETA: J Biol Chem

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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