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Expression of Corticotropin-Releasing Hormone Transgenes in Neurons of Adult and Developing Mice

dc.contributor.authorKeegan, Catherine E.en_US
dc.contributor.authorKarolyi, I. Jillen_US
dc.contributor.authorKnapp, Lauren T.en_US
dc.contributor.authorBourbonais, Francis J.en_US
dc.contributor.authorCamper, Sally A.en_US
dc.contributor.authorSeasholtz, Audrey F.en_US
dc.date.accessioned2006-04-10T17:43:53Z
dc.date.available2006-04-10T17:43:53Z
dc.date.issued1994-12en_US
dc.identifier.citationKeegan, Catherine E., Karolyi, I. Jill, Knapp, Lauren T., Bourbonais, Francis J., Camper, Sally A., Seasholtz, Audrey F. (1994/12)."Expression of Corticotropin-Releasing Hormone Transgenes in Neurons of Adult and Developing Mice." Molecular and Cellular Neuroscience 5(6): 505-514. <http://hdl.handle.net/2027.42/31163>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WNB-45NJCPP-3/2/9e5ba277c1814abccc116e6ccb373ad5en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31163
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7704423&dopt=citationen_US
dc.description.abstractThe DNA sequences important for cell-specific expression and developmental regulation of corticotropin-releasing hormone (CRH) were analyzed in transgenic mice. A construct containing 0.5 kb of CRH 5' flanking DNA linked to the chloramphenicol acetyltransferase reporter gene was expressed in many brain regions and in several ectopic peripheral sites, suggesting that this portion of the CRH gene contains basal promoter activity but lacks DNA elements necessary for appropriate tissue specificity. Cell specificity of transgene expression was examined with a CRH-[beta]-galactosidase reporter construct containing the same 0.5-kb CRH promoter fragment, but also including the CRH structural gene and 2 kb of CRH 3' flanking DNA. Transgene expression was observed in inappropriate regions of the brain, but no expression was detected in peripheral tissues, suggesting that these additional CRH sequences suppress inappropriately high levels of peripheral expression. Cell-specific expression improved significantly with the inclusion of 8.7 kb of CRH 5' flanking DNA. Individual transgenic lines exhibited expression in a number of the major CRH neuronal groups including the paraventricular nucleus, medial geniculate nucleus, inferior olivary nucleus, and Barrington's nucleus. Transgene expression was properly activated in Barrington's nucleus during development. This study demonstrates that the regulatory control of cell-specific and developmentally appropriate CRH expression is complex, utilizing multiple DNA sequence elements located upstream and downstream of the CRH transcription start site.en_US
dc.format.extent870080 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleExpression of Corticotropin-Releasing Hormone Transgenes in Neurons of Adult and Developing 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.affiliationumDepartment of Human Genetics, Graduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.contributor.affiliationumDepartment of Biological Chemistry and Mental Health Research Institute, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.contributor.affiliationumDepartment of Biological Chemistry and Mental Health Research Institute, University of Michigan, Ann Arbor, Michigan 48109-0720, USA.en_US
dc.identifier.pmid7704423en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31163/1/0000062.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/mcne.1994.1062en_US
dc.identifier.sourceMolecular and Cellular Neuroscienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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