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Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation.

Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Research Abstract Details 

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  • Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Abstract Text:

    sunhwa kimSunhwa Kim,takako kogaTakako Koga,miho isobeMiho Isobe,britt e kernBritt E Kern,taeko yokochiTaeko Yokochi,y eugene chinY Eugene Chin,gerard karsentyGerard Karsenty,tadatsugu taniguchiTadatsugu Taniguchi,hiroshi takayanagiHiroshi Takayanagi,

    Bone remodeling is central to maintaining the integrity of the skeletal system, wherein the developed bone is constantly renewed by the balanced action of osteoblastic bone formation and osteoclastic bone resorption. In the present study, we demonstrate a novel function of the Stat1 transcription factor in the regulation of bone remodeling. In the bone of the Stat1-deficient mice, excessive osteoclastogenesis is observed, presumably caused by a loss of negative regulation of osteoclast differentiation by interferon (IFN)-beta. However, the bone mass is unexpectedly increased in these mice. This increase is caused by excessive osteoblast differentiation, wherein Stat1 function is independent of IFN signaling. Actually, Stat1 interacts with Runx2 in its latent form in the cytoplasm, thereby inhibiting the nuclear localization of Runx2, an essential transcription factor for osteoblast differentiation. The new function of Stat1 does not require the Tyr 701 that is phosphorylated when Stat1 becomes a transcriptional activator. Our study provides a unique example in which a latent transcription factor attenuates the activity of another transcription factor in the cytoplasm, and reveals a new regulatory mechanism in bone remodeling.

    Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Publishing Authors By Initials

    s kimS Kim,t kogaT Koga,m isobeM Isobe,be kernBE Kern,t yokochiT Yokochi,ye chinYE Chin,g karsentyG Karsenty,t taniguchiT Taniguchi,h takayanagiH Takayanagi,

    For similar peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta research abstracts see: peptides: intercellular signaling peptides and proteins: cytokines: transforming growth factor beta research

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    Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Journal Published:

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

    Journal: Genes & development

    VOLUME: 17

    Page Numbers: 1979-91

    Journal Abbreviation: Genes Dev.

    ISSN: 0890-9369

    DAY: 15

    MONTH: Aug

    YEAR: 2003

    Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8711660

    Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Keywords Mesh Terms:

    KEYWORDS: Transforming Growth Factor beta

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation. Information

    Substance Name: bone morphogenetic protein 2

    Registry Number: 0

    Grant and Affiliation Information for Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation.

    AFFILIATION: Department of Immunology, Graduate School of Medicine and Faculty of Medicine, University of Tokyo, Tokyo 113-0033, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Genes Dev

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