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dc.contributor.authorStein, Gary S.
dc.contributor.authorStein, Janet L.
dc.contributor.authorLian, Jane B.
dc.contributor.authorVan Wijnen, Andre J.
dc.contributor.authorMontecino, Martin A.
dc.date2022-08-11T08:08:48.000
dc.date.accessioned2022-08-23T16:09:07Z
dc.date.available2022-08-23T16:09:07Z
dc.date.issued1996-08-01
dc.date.submitted2009-01-13
dc.identifier.citationJ Cell Biochem. 1996 Aug;62(2):198-209. <a href="http://dx.doi.org/10.1002/(SICI)1097-4644(199608)62:2andlt;198::AID-JCB8andgt;3.0.CO;2-N">Link to article on publisher's site</a>
dc.identifier.issn0730-2312 (Print)
dc.identifier.doi10.1002/(SICI)1097-4644(199608)62:2andlt;198::AID-JCB8andgt;3.0.CO;2-N
dc.identifier.pmid8844400
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32613
dc.description.abstractMultiple levels of nuclear structure contribute to functional interrelationships with transcriptional control in vivo. The linear organization of gene regulatory sequences is necessary but insufficient to accommodate the requirements for physiological responsiveness to homeostatic, developmental, and tissue-related signals. Chromatin structure, nucleosome organization, and gene-nuclear matrix interactions provide a basis for rendering sequences accessible to transcription factors supporting integration of activities at independent promoter elements of cell cycle- and tissue-specific genes. A model is presented for remodeling of nuclear organization to accommodate developmental transcriptional control.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=8844400&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/(SICI)1097-4644(199608)62:2<198::AID-JCB8>3.0.CO;2-N
dc.subjectAnimals; Cell Cycle; Cell Nucleus; Gene Expression Regulation, Developmental; Humans; *Models, Genetic; Transcription, Genetic
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleFunctional interrelationships between nuclear structure and transcriptional control: contributions to regulation of cell cycle- and tissue-specific gene expression
dc.typeJournal Article
dc.source.journaltitleJournal of cellular biochemistry
dc.source.volume62
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1175
dc.identifier.contextkey693082
html.description.abstract<p>Multiple levels of nuclear structure contribute to functional interrelationships with transcriptional control in vivo. The linear organization of gene regulatory sequences is necessary but insufficient to accommodate the requirements for physiological responsiveness to homeostatic, developmental, and tissue-related signals. Chromatin structure, nucleosome organization, and gene-nuclear matrix interactions provide a basis for rendering sequences accessible to transcription factors supporting integration of activities at independent promoter elements of cell cycle- and tissue-specific genes. A model is presented for remodeling of nuclear organization to accommodate developmental transcriptional control.</p>
dc.identifier.submissionpathgsbs_sp/1175
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages198-209


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