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    Inducible changes in cell size and attachment area due to expression of a mutant SWI/SNF chromatin remodeling enzyme

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    Authors
    Hill, David A.
    Chiosea, Simion I.
    Jamaluddin, Saha
    Roy, Kanaklata
    Fischer, Andrew H.
    Boyd, Douglas D.
    Nickerson, Jeffrey A.
    Imbalzano, Anthony N.
    UMass Chan Affiliations
    Department of Pathology
    Department of Cell Biology
    Document Type
    Journal Article
    Publication Date
    2004-11-13
    Keywords
    Actins
    Adenosine Triphosphatases
    Adenosine Triphosphate
    Animals
    Blotting, Northern
    Blotting, Western
    Cell Adhesion
    Cell Differentiation
    Cell Line
    Cell Line, Tumor
    Cell Nucleus
    Cell Size
    Chromatin
    Collagen
    Cytoskeletal Proteins
    Cytoskeleton
    DNA Helicases
    DNA, Complementary
    Dose-Response Relationship, Drug
    Drug Combinations
    Focal Adhesions
    Gene Expression Regulation
    Heterozygote
    Humans
    Laminin
    Mice
    Mutation
    Neoplasm Metastasis
    Nuclear Proteins
    Paxillin
    Phosphoproteins
    Protein Binding
    Protein Structure, Tertiary
    Proteoglycans
    RNA, Messenger
    Receptors, Cell Surface
    Time Factors
    Transcription Factors
    Cell Biology
    Life Sciences
    Medicine and Health Sciences
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    Abstract
    The SWI/SNF enzymes belong to a family of ATP-dependent chromatin remodeling enzymes that have been functionally implicated in gene regulation, development, differentiation and oncogenesis. BRG1, the catalytic core subunit of some of the SWI/SNF enzymes, can interact with known tumor suppressor proteins and can act as a tumor suppressor itself. We report that cells that inducibly express ATPase-deficient versions of BRG1 increase in cell volume, area of attachment and nuclear size upon expression of the mutant BRG1 protein. Examination of focal adhesions reveals qualitative changes in paxillin distribution but no difference in the actin cytoskeletal structure. Increases in cell size and shape correlate with over-expression of two integrins and the urokinase-type plasminogen activator receptor (uPAR), which is also involved in cell adhesion and is often over-expressed in metastatic cancer cells. These findings demonstrate that gene expression pathways affected by chromatin remodeling enzymes can regulate the physical dimensions of mammalian cell morphology.
    Source
    J Cell Sci. 2004 Nov 15;117(Pt 24):5847-54. Link to article on publisher's site
    DOI
    10.1242/jcs.01502
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/42645
    PubMed ID
    15537831
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1242/jcs.01502
    Scopus Count
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    UMass Chan Faculty and Researcher Publications

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