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Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence.

Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Research Abstract Details 

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  • Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Abstract Text:

    larisa litovchickLarisa Litovchick,subhashini sadasivamSubhashini Sadasivam,laurence florensLaurence Florens,xiaopeng zhuXiaopeng Zhu,selene k swansonSelene K Swanson,soundarapandian velmuruganSoundarapandian Velmurugan,runsheng chenRunsheng Chen,michael p washburnMichael P Washburn,x shirley liuX Shirley Liu,james a decaprioJames A DeCaprio,

    The mammalian Retinoblastoma (RB) family including pRB, p107, and p130 represses E2F target genes through mechanisms that are not fully understood. In D. melanogaster, RB-dependent repression is mediated in part by the multisubunit protein complex Drosophila RBF, E2F, and Myb (dREAM) that contains homologs of the C. elegans synthetic multivulva class B (synMuvB) gene products. Using an integrated approach combining proteomics, genomics, and bioinformatic analyses, we identified a p130 complex termed DP, RB-like, E2F, and MuvB (DREAM) that contains mammalian homologs of synMuvB proteins LIN-9, LIN-37, LIN-52, LIN-54, and LIN-53/RBBP4. DREAM bound to more than 800 human promoters in G0 and was required for repression of E2F target genes. In S phase, MuvB proteins dissociated from p130 and formed a distinct submodule that bound MYB. This work reveals an evolutionarily conserved multisubunit protein complex that contains p130 and E2F4, but not pRB, and mediates the repression of cell cycle-dependent genes in quiescence.

    Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Publishing Authors By Initials

    l litovchickL Litovchick,s sadasivamS Sadasivam,l florensL Florens,x zhuX Zhu,sk swansonSK Swanson,s velmuruganS Velmurugan,r chenR Chen,mp washburnMP Washburn,xs liuXS Liu,ja decaprioJA DeCaprio,

    For similar genetic processes: mutagenesis: suppression, genetic research abstracts see: genetic processes: mutagenesis: suppression, genetic research

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    Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Molecular cell

    VOLUME: 26

    Page Numbers: 539-51

    Journal Abbreviation: Mol. Cell

    ISSN: 1097-2765

    DAY: 25

    MONTH: May

    YEAR: 2007

    Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9802571

    Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Keywords Mesh Terms:

    KEYWORDS: Suppression, Genetic

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence. Information

    Substance Name: Retinoblastoma-Like Protein p130

    Registry Number: 0

    Grant and Affiliation Information for Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence.

    AFFILIATION: Department of Medical Oncology, Dana-Farber Cancer Institute and Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA063113

    ACRONYM: CA

    MEDLINETA: Mol Cell

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    Evolutionarily conserved multisubunit RBL2/p130 and E2F4 protein complex represses human cell cycle-dependent genes in quiescence Related Publications

     

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