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dc.contributor.authorImbalzano, Karen M.
dc.contributor.authorCohet, Nathalie
dc.contributor.authorWu, Qiong
dc.contributor.authorUnderwood, Jean M.
dc.contributor.authorImbalzano, Anthony N.
dc.contributor.authorNickerson, Jeffrey A.
dc.date2022-08-11T08:08:03.000
dc.date.accessioned2022-08-23T15:40:35Z
dc.date.available2022-08-23T15:40:35Z
dc.date.issued2013-02-06
dc.date.submitted2013-03-22
dc.identifier.citationPLoS One. 2013;8(2):e55628. doi: 10.1371/journal.pone.0055628. Epub 2013 Feb 6. <a href="http://dx.doi.org/10.1371/journal.pone.0055628">Link to article on publisher's site</a>
dc.identifier.issn1932-6203 (Linking)
dc.identifier.doi10.1371/journal.pone.0055628
dc.identifier.pmid23405182
dc.identifier.urihttp://hdl.handle.net/20.500.14038/26434
dc.description.abstractChanges in nuclear morphology occur during normal development and have been observed during the progression of several diseases. The shape of a nucleus is governed by the balance of forces exerted by nuclear-cytoskeletal contacts and internal forces created by the structure of the chromatin and nuclear envelope. However, factors that regulate the balance of these forces and determine nuclear shape are poorly understood. The SWI/SNF chromatin remodeling enzyme ATPase, BRG1, has been shown to contribute to the regulation of overall cell size and shape. Here we document that immortalized mammary epithelial cells show BRG1-dependent nuclear shape changes. Specifically, knockdown of BRG1 induced grooves in the nuclear periphery that could be documented by cytological and ultrastructural methods. To test the hypothesis that the observed changes in nuclear morphology resulted from altered tension exerted by the cytoskeleton, we disrupted the major cytoskeletal networks and quantified the frequency of BRG1-dependent changes in nuclear morphology. The results demonstrated that disruption of cytoskeletal networks did not change the frequency of BRG1-induced nuclear shape changes. These findings suggest that BRG1 mediates control of nuclear shape by internal nuclear mechanisms that likely control chromatin dynamics.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23405182&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>Copyright 2013 Imbalzano et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</p>
dc.subjectCell Nucleus Shape
dc.subjectCytoskeletal Proteins
dc.subjectCytoskeleton
dc.subjectDNA Helicases
dc.subjectNuclear Proteins
dc.subjectTranscription Factors
dc.subjectCell and Developmental Biology
dc.subjectCell Biology
dc.subjectMolecular Biology
dc.titleNuclear Shape Changes Are Induced by Knockdown of the SWI/SNF ATPase BRG1 and Are Independent of Cytoskeletal Connections
dc.typeJournal Article
dc.source.journaltitlePloS one
dc.source.volume8
dc.source.issue2
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1115&amp;context=cellbiology_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/cellbiology_pp/116
dc.identifier.contextkey3943377
refterms.dateFOA2022-08-23T15:40:35Z
html.description.abstract<p>Changes in nuclear morphology occur during normal development and have been observed during the progression of several diseases. The shape of a nucleus is governed by the balance of forces exerted by nuclear-cytoskeletal contacts and internal forces created by the structure of the chromatin and nuclear envelope. However, factors that regulate the balance of these forces and determine nuclear shape are poorly understood. The SWI/SNF chromatin remodeling enzyme ATPase, BRG1, has been shown to contribute to the regulation of overall cell size and shape. Here we document that immortalized mammary epithelial cells show BRG1-dependent nuclear shape changes. Specifically, knockdown of BRG1 induced grooves in the nuclear periphery that could be documented by cytological and ultrastructural methods. To test the hypothesis that the observed changes in nuclear morphology resulted from altered tension exerted by the cytoskeleton, we disrupted the major cytoskeletal networks and quantified the frequency of BRG1-dependent changes in nuclear morphology. The results demonstrated that disruption of cytoskeletal networks did not change the frequency of BRG1-induced nuclear shape changes. These findings suggest that BRG1 mediates control of nuclear shape by internal nuclear mechanisms that likely control chromatin dynamics.</p>
dc.identifier.submissionpathcellbiology_pp/116
dc.contributor.departmentDepartment of Cell and Developmental Biology
dc.source.pagese55628


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