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dc.contributor.authorHill, David A.
dc.contributor.authorChiosea, Simion I.
dc.contributor.authorJamaluddin, Saha
dc.contributor.authorRoy, Kanaklata
dc.contributor.authorFischer, Andrew H.
dc.contributor.authorBoyd, Douglas D.
dc.contributor.authorNickerson, Jeffrey A.
dc.contributor.authorImbalzano, Anthony N.
dc.date2022-08-11T08:10:05.000
dc.date.accessioned2022-08-23T16:55:06Z
dc.date.available2022-08-23T16:55:06Z
dc.date.issued2004-11-13
dc.date.submitted2008-10-31
dc.identifier.citationJ Cell Sci. 2004 Nov 15;117(Pt 24):5847-54. <a href="http://dx.doi.org/10.1242/jcs.01502">Link to article on publisher's site</a>
dc.identifier.issn0021-9533 (Print)
dc.identifier.doi10.1242/jcs.01502
dc.identifier.pmid15537831
dc.identifier.urihttp://hdl.handle.net/20.500.14038/42645
dc.description.abstractThe 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15537831&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectActins
dc.subjectAdenosine Triphosphatases
dc.subjectAdenosine Triphosphate
dc.subjectAnimals
dc.subjectBlotting, Northern
dc.subjectBlotting, Western
dc.subjectCell Adhesion
dc.subjectCell Differentiation
dc.subjectCell Line
dc.subjectCell Line, Tumor
dc.subjectCell Nucleus
dc.subjectCell Size
dc.subjectChromatin
dc.subjectCollagen
dc.subjectCytoskeletal Proteins
dc.subjectCytoskeleton
dc.subjectDNA Helicases
dc.subjectDNA, Complementary
dc.subjectDose-Response Relationship, Drug
dc.subjectDrug Combinations
dc.subjectFocal Adhesions
dc.subjectGene Expression Regulation
dc.subjectHeterozygote
dc.subjectHumans
dc.subjectLaminin
dc.subjectMice
dc.subjectMutation
dc.subjectNeoplasm Metastasis
dc.subjectNuclear Proteins
dc.subjectPaxillin
dc.subjectPhosphoproteins
dc.subjectProtein Binding
dc.subjectProtein Structure, Tertiary
dc.subjectProteoglycans
dc.subjectRNA, Messenger
dc.subjectReceptors, Cell Surface
dc.subjectTime Factors
dc.subjectTranscription Factors
dc.subjectCell Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleInducible changes in cell size and attachment area due to expression of a mutant SWI/SNF chromatin remodeling enzyme
dc.typeJournal Article
dc.source.journaltitleJournal of cell science
dc.source.volume117
dc.source.issuePt 24
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1973&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/974
dc.identifier.contextkey659156
refterms.dateFOA2022-08-23T16:55:07Z
html.description.abstract<p>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.</p>
dc.identifier.submissionpathoapubs/974
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages5847-54


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