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dc.contributor.authorBagchi, Mihir
dc.contributor.authorAnsari, Shamim A.
dc.contributor.authorLindenmuth, Danielle M.
dc.contributor.authorVan Wijnen, Andre J.
dc.contributor.authorLian, Jane B.
dc.contributor.authorStein, Janet L.
dc.contributor.authorStein, Gary S.
dc.date2022-08-11T08:09:00.000
dc.date.accessioned2022-08-23T16:15:05Z
dc.date.available2022-08-23T16:15:05Z
dc.date.issued1998-04-16
dc.date.submitted2008-07-02
dc.identifier.citation<p>Mol Biol Rep. 1998 Jan;25(1):13-9.</p>
dc.identifier.issn0301-4851 (Print)
dc.identifier.doi10.1023/A:1006886110771
dc.identifier.pmid9540063
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34007
dc.description.abstractAssociation of transcription factors with the nuclear matrix represents a mechanism by which nuclear architecture may influence transcriptional control of gene expression. This investigation examines nuclear matrix associated proteins (NMP's) isolated from ocular lens epithelial cells by monitoring DNA binding activities using consensus oligonucleotides recognized by the transcription factors YY1, AML-1, AP-1, SP-1 and ATF. The nuclear matrix fractions tested included an immortilized human lens epithelial cell line containing the SV40 large T-antigen, and two mouse lens epithelial cell lines derived from either a normal mouse or a cataract mouse. A rabbit epidermal epithelial cell line and HeLa cells were also included in this study for comparison. The data from these experiments reveal that ubiquitously represented and tissue restricted regulatory proteins are associated with nuclear matrix of lens epithelial cells. The functional significance of the nuclear matrix association of these transcription factors remains to be determined. However, our findings raise the possibility that the transcription factors associated with the nuclear matrix could have specific roles in gene regulation and eye tissue development.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9540063&dopt=Abstract ">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1023/A:1006886110771
dc.subjectAnimals; Antigens, Nuclear; Cataract; Cell Extracts; Cell Line; Cell Nucleus; DNA; DNA-Binding Proteins; Epithelial Cells; Eye Proteins; Humans; Lens, Crystalline; Mice; Mice, Inbred BALB C; Nuclear Matrix; Nuclear Proteins; Transcription Factors
dc.subjectCell Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleNuclear matrix associated DNA-binding proteins of ocular lens epithelial cells
dc.typeJournal Article
dc.source.journaltitleMolecular biology reports
dc.source.volume25
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/66
dc.identifier.contextkey542478
html.description.abstract<p>Association of transcription factors with the nuclear matrix represents a mechanism by which nuclear architecture may influence transcriptional control of gene expression. This investigation examines nuclear matrix associated proteins (NMP's) isolated from ocular lens epithelial cells by monitoring DNA binding activities using consensus oligonucleotides recognized by the transcription factors YY1, AML-1, AP-1, SP-1 and ATF. The nuclear matrix fractions tested included an immortilized human lens epithelial cell line containing the SV40 large T-antigen, and two mouse lens epithelial cell lines derived from either a normal mouse or a cataract mouse. A rabbit epidermal epithelial cell line and HeLa cells were also included in this study for comparison. The data from these experiments reveal that ubiquitously represented and tissue restricted regulatory proteins are associated with nuclear matrix of lens epithelial cells. The functional significance of the nuclear matrix association of these transcription factors remains to be determined. However, our findings raise the possibility that the transcription factors associated with the nuclear matrix could have specific roles in gene regulation and eye tissue development.</p>
dc.identifier.submissionpathgsbs_sp/66
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages13-9


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