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dc.contributor.authorBruschweiler-Li, Lei
dc.contributor.authorFuentes Medel, Yuly F.
dc.contributor.authorScofield, Michael D.
dc.contributor.authorTrang, Ellen B. T.
dc.contributor.authorBinke, Sarah A.
dc.contributor.authorGardner, Paul D.
dc.date2022-08-11T08:08:53.000
dc.date.accessioned2022-08-23T16:11:09Z
dc.date.available2022-08-23T16:11:09Z
dc.date.issued2010-03-31
dc.date.submitted2010-05-10
dc.identifier.citation<p>Bruschweiler-Li L, Medel YF, Scofield MD, Trang EB, Binke SA, Gardner PD (2010) Temporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter. Neuroscience 166:864-877.</p>
dc.identifier.issn1873-7544
dc.identifier.doi10.1016/j.neuroscience.2010.01.026
dc.identifier.pmid20096338
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33100
dc.description.abstractSignaling through nicotinic acetylcholine (nACh) receptors underlies a diverse array of behaviors. In order for appropriate signaling to occur via nACh receptors, it is necessary for the genes encoding the receptor subunits to be expressed in a highly regulated temporal and spatial manner. Here we report a transgenic mouse approach to characterize the transcriptional regulation of the gene encoding the nACh receptor beta4 subunit. nACh receptors containing this subunit play critical roles in both the central and peripheral nervous systems. We demonstrate that a 2.3-kilobase pair fragment of the beta4 5'-flanking region is capable of directing reporter gene expression in transgenic animals. Importantly, the transcriptional activity of the promoter region is cell-type-specific and developmentally regulated and overlaps to a great extent with endogenous beta4 mRNA expression. These data indicate that the 2.3-kilobase pair fragment contains transcriptional regulatory elements critical for appropriate beta4 subunit gene expression.
dc.language.isoen_US
dc.publisherElsevier Science
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=20096338&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837126/
dc.subjectReceptors, Nicotinic; Gene Expression Regulation; Transcription, Genetic
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleTemporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter.
dc.typeJournal Article
dc.source.journaltitleNeuroscience
dc.source.volume166
dc.source.issue3
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2646&amp;context=gsbs_sp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1644
dc.identifier.contextkey1303573
refterms.dateFOA2022-08-23T16:11:09Z
html.description.abstract<p>Signaling through nicotinic acetylcholine (nACh) receptors underlies a diverse array of behaviors. In order for appropriate signaling to occur via nACh receptors, it is necessary for the genes encoding the receptor subunits to be expressed in a highly regulated temporal and spatial manner. Here we report a transgenic mouse approach to characterize the transcriptional regulation of the gene encoding the nACh receptor beta4 subunit. nACh receptors containing this subunit play critical roles in both the central and peripheral nervous systems. We demonstrate that a 2.3-kilobase pair fragment of the beta4 5'-flanking region is capable of directing reporter gene expression in transgenic animals. Importantly, the transcriptional activity of the promoter region is cell-type-specific and developmentally regulated and overlaps to a great extent with endogenous beta4 mRNA expression. These data indicate that the 2.3-kilobase pair fragment contains transcriptional regulatory elements critical for appropriate beta4 subunit gene expression.</p>
dc.identifier.submissionpathgsbs_sp/1644
dc.contributor.departmentGardner Lab
dc.contributor.departmentGraduate School of Biomedical Sciences, Neuroscience Program
dc.contributor.departmentNeurobiology
dc.contributor.departmentBrudnick Neuropsychiatric Research Institute
dc.contributor.departmentGraduate School of Biomedical Sciences, Interdisciplinary Graduate Program
dc.contributor.departmentPsychiatry
dc.source.pages864-877
dc.contributor.studentYuly F. Fuentes Medel; Michael D. Scofield


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