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dc.contributor.authorXiao, Hengyi
dc.contributor.authorLeBlanc, Scott E.
dc.contributor.authorWu, Qiong
dc.contributor.authorKonda, Silvana
dc.contributor.authorSalma, Nunciada
dc.contributor.authorMarfella, Concetta G. A.
dc.contributor.authorOhkawa, Yasuyuki
dc.contributor.authorImbalzano, Anthony N.
dc.date2022-08-11T08:09:08.000
dc.date.accessioned2022-08-23T16:18:35Z
dc.date.available2022-08-23T16:18:35Z
dc.date.issued2011-01-14
dc.date.submitted2011-02-08
dc.identifier.citationJ Cell Physiol. 2011 Jan;226(1):86-93. <a href="http://dx.doi.org/10.1002/jcp.22308">Link to article on publisher's site</a>
dc.identifier.issn0021-9541 (Linking)
dc.identifier.doi10.1002/jcp.22308
dc.identifier.pmid20625991
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34849
dc.description.abstractThe nuclear hormone receptor peroxisome proliferator activated receptor gamma (PPARgamma) is a ligand-activated transcription factor that specifies formation of the adipocyte lineage. PPARgamma also serves as a primary target for the treatment of type 2 diabetes, illustrating both its medical relevance as well as the need to understand fundamental aspects of PPARgamma expression and function. Here, we characterize molecular changes that occur at the PPARgamma2 promoter within the first several hours of adipocyte differentiation in culture. Our results demonstrate that changes in chromatin accessibility at the PPARgamma2 promoter and occupancy of the promoter by the c-Fos transcription factor occur within an hour of the onset of differentiation, followed closely by the binding of the CCAAT/Enhancer Binding Protein beta (C/EBPbeta) transcription factor. All three events show a remarkable dependency on protein kinase A (PKA) activity. These results reflect novel requirements for the PKA signaling pathway and reinforce the importance of PKA function during the onset of adipocyte differentiation. J. Cell. Physiol. (c) 2010 Wiley-Liss, Inc.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20625991&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/jcp.22308
dc.subjectAdipogenesis
dc.subjectChromatin
dc.subjectCyclic AMP-Dependent Protein Kinases
dc.subjectPPAR gamma
dc.subjectPromoter Regions, Genetic
dc.subjectTranscription Factors
dc.subjectCell Biology
dc.titleChromatin accessibility and transcription factor binding at the PPARgamma2 promoter during adipogenesis is protein kinase a-dependent
dc.typeJournal Article
dc.source.journaltitleJournal of cellular physiology
dc.source.volume226
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/imbalzano/1
dc.identifier.contextkey1771155
html.description.abstract<p>The nuclear hormone receptor peroxisome proliferator activated receptor gamma (PPARgamma) is a ligand-activated transcription factor that specifies formation of the adipocyte lineage. PPARgamma also serves as a primary target for the treatment of type 2 diabetes, illustrating both its medical relevance as well as the need to understand fundamental aspects of PPARgamma expression and function. Here, we characterize molecular changes that occur at the PPARgamma2 promoter within the first several hours of adipocyte differentiation in culture. Our results demonstrate that changes in chromatin accessibility at the PPARgamma2 promoter and occupancy of the promoter by the c-Fos transcription factor occur within an hour of the onset of differentiation, followed closely by the binding of the CCAAT/Enhancer Binding Protein beta (C/EBPbeta) transcription factor. All three events show a remarkable dependency on protein kinase A (PKA) activity. These results reflect novel requirements for the PKA signaling pathway and reinforce the importance of PKA function during the onset of adipocyte differentiation. J. Cell. Physiol. (c) 2010 Wiley-Liss, Inc.</p>
dc.identifier.submissionpathimbalzano/1
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages86-93


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