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Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity.

Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Research Abstract Details 

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  • Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Abstract Text:

    david p sparlingDavid P Sparling,beth a grieselBeth A Griesel,ann louise olsonAnn Louise Olson,

    GLUT4 promoter activity is regulated by hormonal, metabolic, and tissue-specific controls. This complicates the study of GLUT4 gene transcription, as no cell culture model adequately recapitulates these extracellular regulators. While investigating cultured primary adipocytes as a model system for GLUT4 transcription, we observed that GLUT4 mRNA was specifically and rapidly downregulated upon tissue dispersal. Downregulation of GLUT4 mRNA was mediated in part by loss of regulatory control by the trans-acting factors that control GLUT4 transcriptional activity [the myocyte enhancer factor 2 (MEF2) transcription factor family and the GLUT4 enhancer factor] and their cognate DNA binding sites in transgenic mice. The differences in GLUT4 transcription when whole adipose tissue and cell culture model systems are compared can be correlated to a posttranslational phosphorylation of the transcription factor MEF2A. The difference in the MEF2A phosphorylation state in whole tissue vs. isolated cells may provide a further basis for the development of an in vitro system that could recapitulate fully regulated GLUT4 promoter activity. Development of an in vitro system to reconstitute GLUT4 transcriptional regulation will further efforts to discern the molecular mechanisms that underlie GLUT4 expression.

    Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Publishing Authors By Initials

    dp sparlingDP Sparling,ba grieselBA Griesel,al olsonAL Olson,

    For similar genetic processes: gene expression: transcription, genetic research abstracts see: genetic processes: gene expression: transcription, genetic research

    PUBMED ID PMID:

    MEDLINE DATE:

    Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Journal Published:

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

    Journal: American journal of physiology. Endocrinology and

    VOLUME: 292

    Page Numbers: E1149-56

    Journal Abbreviation: Am. J. Physiol. Endocrinol. Me

    ISSN: 0193-1849

    DAY: 12

    MONTH: 12

    YEAR: 2006

    Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100901226

    Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Keywords Mesh Terms:

    KEYWORDS: Transcription, Genetic

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity. Information

    Substance Name: Myogenic Regulatory Factors

    Registry Number: 0

    Grant and Affiliation Information for Hyperphosphorylation of MEF2A in primary adipocytes correlates with downregulation of human GLUT4 gene promoter activity.

    AFFILIATION: Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, PO Box 26901, Rm. 853-BMSB, Oklahoma City, OK 73190, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: DK-68438

    ACRONYM: DK

    MEDLINETA: Am J Physiol Endocrinol Metab

    REFSOURCE:

    DATABASENAME:

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    Number Hits: 0

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