Mammalian SWI/SNF complexes promote MyoD-mediated muscle differentiation
dc.contributor.author | de la Serna, Ivana L. | |
dc.contributor.author | Carlson, Kerri A. | |
dc.contributor.author | Imbalzano, Anthony N. | |
dc.date | 2022-08-11T08:09:08.000 | |
dc.date.accessioned | 2022-08-23T16:18:40Z | |
dc.date.available | 2022-08-23T16:18:40Z | |
dc.date.issued | 2001-02-15 | |
dc.date.submitted | 2011-02-09 | |
dc.identifier.citation | Nat Genet. 2001 Feb;27(2):187-90. <a href="http://dx.doi.org/10.1038/84826">Link to article on publisher's site</a> | |
dc.identifier.issn | 1061-4036 (Linking) | |
dc.identifier.doi | 10.1038/84826 | |
dc.identifier.pmid | 11175787 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/34868 | |
dc.description.abstract | Mammalian SWI/SNF complexes are ATP-dependent chromatin remodeling enzymes that have been implicated in the regulation of gene expression, cell-cycle control and oncogenesis. MyoD is a muscle-specific regulator able to induce myogenesis in numerous cell types. To ascertain the requirement for chromatin remodeling enzymes in cellular differentiation processes, we examined MyoD-mediated induction of muscle differentiation in fibroblasts expressing dominant-negative versions of the human brahma-related gene-1 (BRG1) or human brahma (BRM), the ATPase subunits of two distinct SWI/SNF enzymes. We find that induction of the myogenic phenotype is completely abrogated in the presence of the mutant enzymes. We further demonstrate that failure to induce muscle-specific gene expression correlates with inhibition of chromatin remodeling in the promoter region of an endogenous muscle-specific gene. Our results demonstrate that SWI/SNF enzymes promote MyoD-mediated muscle differentiation and indicate that these enzymes function by altering chromatin structure in promoter regions of endogenous, differentiation-specific loci. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=11175787&dopt=Abstract">Link to Article in PubMed</a> | |
dc.relation.url | http://dx.doi.org/10.1038/84826 | |
dc.subject | Adenosine Triphosphatases | |
dc.subject | Animals | |
dc.subject | Cell Differentiation | |
dc.subject | DNA Helicases | |
dc.subject | Gene Expression Regulation | |
dc.subject | Mice | |
dc.subject | Muscles | |
dc.subject | MyoD Protein | |
dc.subject | Nuclear Proteins | |
dc.subject | Promoter Regions, Genetic | |
dc.subject | Transcription Factors | |
dc.subject | Cell Biology | |
dc.title | Mammalian SWI/SNF complexes promote MyoD-mediated muscle differentiation | |
dc.type | Journal Article | |
dc.source.journaltitle | Nature genetics | |
dc.source.volume | 27 | |
dc.source.issue | 2 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/imbalzano/9 | |
dc.identifier.contextkey | 1773785 | |
html.description.abstract | <p>Mammalian SWI/SNF complexes are ATP-dependent chromatin remodeling enzymes that have been implicated in the regulation of gene expression, cell-cycle control and oncogenesis. MyoD is a muscle-specific regulator able to induce myogenesis in numerous cell types. To ascertain the requirement for chromatin remodeling enzymes in cellular differentiation processes, we examined MyoD-mediated induction of muscle differentiation in fibroblasts expressing dominant-negative versions of the human brahma-related gene-1 (BRG1) or human brahma (BRM), the ATPase subunits of two distinct SWI/SNF enzymes. We find that induction of the myogenic phenotype is completely abrogated in the presence of the mutant enzymes. We further demonstrate that failure to induce muscle-specific gene expression correlates with inhibition of chromatin remodeling in the promoter region of an endogenous muscle-specific gene. Our results demonstrate that SWI/SNF enzymes promote MyoD-mediated muscle differentiation and indicate that these enzymes function by altering chromatin structure in promoter regions of endogenous, differentiation-specific loci.</p> | |
dc.identifier.submissionpath | imbalzano/9 | |
dc.contributor.department | Department of Cell Biology | |
dc.source.pages | 187-90 |