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Distant regulatory elements in a Sox10-ΒGEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues

dc.contributor.authorDeal, Karen K.en_US
dc.contributor.authorCantrell, V. Ashleyen_US
dc.contributor.authorChandler, Ronald L.en_US
dc.contributor.authorSaunders, Thomas L.en_US
dc.contributor.authorMortlock, Douglas P.en_US
dc.contributor.authorSouthard-Smith, E. Michelleen_US
dc.date.accessioned2007-01-17T15:54:40Z
dc.date.available2007-01-17T15:54:40Z
dc.date.issued2006en_US
dc.identifier.citationDeal, Karen K.; Cantrell, V. Ashley; Chandler, Ronald L.; Saunders, Thomas L.; Mortlock, Douglas P.; Southard-Smith, E. Michelle (2006)."Distant regulatory elements in a Sox10-ΒGEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues." Developmental Dynamics 9999(9999): NA-NA. <http://hdl.handle.net/2027.42/49298>en_US
dc.identifier.issn1058-8388en_US
dc.identifier.issn1097-0177en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/49298
dc.description.abstractSox10 is an essential transcription factor required for development of neural crest-derived melanocytes, peripheral glia, and enteric ganglia. Multiple transcriptional targets regulated by Sox10 have been identified; however, little is known regarding regulation of Sox10 . High sequence conservation surrounding 5′ exons 1 through 3 suggests these regions might contain functional regulatory elements. However, we observed that these Sox10 genomic sequences do not confer appropriate cell-specific transcription in vitro when linked to a heterologous reporter. To identify elements required for expression of Sox10 in vivo, we modified bacterial artificial chromosomes (BACs) to generate a Sox10 ΒGeoBAC transgene. Our approach leaves endogenous Sox10 loci unaltered, circumventing haploinsufficiency issues that arise from gene targeting. Sox10 ΒGeoBAC expression closely approximates Sox10 expression in vivo, resulting in expression in anterior dorsal neural tube at embryonic day (E) 8.5 and in cranial ganglia, otic vesicle, and developing dorsal root ganglia at E10.5. Characterization of Sox10 ΒGeoBAC expression confirms the presence of essential regulatory regions and additionally identifies previously unreported expression in thyroid parafollicular cells, thymus, salivary, adrenal, and lacrimal glands. Fortuitous deletions in independent Sox10 ΒGeoBAC lines result in loss of transgene expression in peripheral nervous system lineages and coincide with evolutionarily conserved regions. Our analysis indicates that Sox10 expression requires the presence of distant cis -acting regulatory elements. The Sox10 ΒGeoBAC transgene offers one avenue for specifically testing the role of individual conserved regions in regulation of Sox10 and makes possible analysis of Sox10+ derivatives in the context of normal neural crest development. Developmental Dynamics, 2006. © 2006 Wiley-Liss, Inc.en_US
dc.format.extent400823 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley-Liss, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCell & Developmental Biologyen_US
dc.titleDistant regulatory elements in a Sox10-ΒGEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissuesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Molecular Medicine and Genetics, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDivision of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennesseeen_US
dc.contributor.affiliationotherDivision of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennesseeen_US
dc.contributor.affiliationotherDivision of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennesseeen_US
dc.contributor.affiliationotherDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennesseeen_US
dc.contributor.affiliationotherDivision of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee ; Division of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, 529 Light Hall, 2215 Garland Avenue, Nashville, TN 37232-0275en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/49298/1/899_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/dvdy.20769en_US
dc.identifier.sourceDevelopmental Dynamicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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