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Tissue-specific expression of the human neuropeptide Y gene in transgenic mice

dc.contributor.authorWaldbieser, Geoffrey C.en_US
dc.contributor.authorMinth, Carolyn D.en_US
dc.contributor.authorChrisman, C. Larryen_US
dc.contributor.authorDixon, Jack E.en_US
dc.date.accessioned2006-04-10T15:10:57Z
dc.date.available2006-04-10T15:10:57Z
dc.date.issued1992-06en_US
dc.identifier.citationWaldbieser, Geoffrey C., Minth, Carolyn D., Chrisman, C. Larry, Dixon, Jack E. (1992/06)."Tissue-specific expression of the human neuropeptide Y gene in transgenic mice." Molecular Brain Research 14(1-2): 87-93. <http://hdl.handle.net/2027.42/29991>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T07-484F2HF-3H/2/31fc2472ebe0a079db4de5d12b6c7988en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29991
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1323021&dopt=citationen_US
dc.description.abstractNeuropeptide Y (NPY) is the most abundant neuropeptide detected in the mammalian brain, and is found throughout the central and peripheral nervous systems. This peptide is a proposed regulator of appetite, blood pressure, and pituitary hormone release. Previous experiments have demonstrated the ability of 5' sequences within the human NPY gene to promote transcription in cultured neuronal cells. To identify sequences in this gene that regulate tissue-specific expression, a NPY/CAT fusion gene, containing approximately 850 bp of NPY sequences, was microinjected into fertilized mouse ova. Five lines of transgenic mice were derived from these ova and several tissues from mice of each line were tested for transgene expression using the CAT assay. One line demonstrated X-chromosome-linked transmission of the transgene while the other lines demonstrated autosomally-linked transmission. Three lines demonstrated transgene expression with significant levels of CAT activity detectable only in tissues which have been shown to express endogenous NPY. One autosomally-linked line did not demonstrate significant levels of transgene activity because the transgene appeared to have undergone structural alteration during genomic integration. No transgene activity was detected in either male of female mice from the X-linked line, suggesting a positional regulation of the transgene locus other than X-inactivation in this line. The present research demonstrated the NPY regulatory sequences included i in pCATNPY[Delta]796 sufficiently directed tissue-appropriate gene expression in transgenic mice.en_US
dc.format.extent703754 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleTissue-specific expression of the human neuropeptide Y gene in transgenic miceen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepatment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Biochemistry, Purdue University, West Lafayette, IN 47907, USA.en_US
dc.contributor.affiliationumDepatment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Biochemistry, Purdue University, West Lafayette, IN 47907, USA.en_US
dc.contributor.affiliationotherDepartment of Animal Sciences, Purdue University, West Lafayette, IN 47907, USAen_US
dc.contributor.affiliationotherdeceaseden_US
dc.identifier.pmid1323021en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29991/1/0000358.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0169-328X(92)90014-3en_US
dc.identifier.sourceMolecular Brain Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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