Temporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter.
Biochemistry & Molecular Pharmacology
Graduate School of Biomedical Sciences, Interdisciplinary Graduate Program; Department of Psychiatry, Brudnick Neuropsychiatric Research Institute; Department of Neurobiology; Program in Neuroscience
Life Sciences | Medicine and Health Sciences
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.
DOI of Published Version
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.
Bruschweiler-Li L, Fuentes 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.. GSBS Student Publications. https://doi.org/10.1016/j.neuroscience.2010.01.026. Retrieved from https://escholarship.umassmed.edu/gsbs_sp/1644