Publication
Phox2b function in the enteric nervous system is conserved in zebrafish and is sox10-dependent
| dc.contributor.author | Elworthy, S. | |
| dc.contributor.author | P Pinto, Jorge | |
| dc.contributor.author | Pettifer, A. | |
| dc.contributor.author | Leonor Cancela, M. | |
| dc.contributor.author | Kelsh, R. N. | |
| dc.date.accessioned | 2018-12-07T14:57:50Z | |
| dc.date.available | 2018-12-07T14:57:50Z | |
| dc.date.issued | 2005-05 | |
| dc.description.abstract | Zebrafish lacking functional sox10 have defects in non-ectomesenchymal neural crest derivatives including the enteric nervous system (ENS) and as such provide an animal model for human Waardenburg Syndrome IV. Here, we characterize zebrafish phox2b as a functionally conserved marker of the developing ENS. We show that morpholino-mediated knockdown of Phox2b generates fish modeling Hirschsprung disease. Using markers, including phox2b, we investigate the ontogeny of the sox10 ENS phenotype. As previously shown for melanophore development, ENS progenitor fate specification fails in these mutant fish. However, in addition, we trace back the sox10 mutant ENS defect to an even earlier time point, finding that most neural crest cells fail to migrate ventrally to the gut primordium. (c) 2005 Elsevier Ireland Ltd. All rights reserved. | |
| dc.description.sponsorship | Medical Research Council [G0300415] | |
| dc.identifier.doi | 10.1016/j.mod.2004.12.008 | |
| dc.identifier.issn | 0925-4773 | |
| dc.identifier.issn | 1872-6356 | |
| dc.identifier.uri | http://hdl.handle.net/10400.1/11721 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | |
| dc.publisher | Elsevier Science | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Transcription factor sox10 | |
| dc.subject | Isolated hirschsprung disease | |
| dc.subject | Neural crest derivatives | |
| dc.subject | Receptor tyrosine kinase | |
| dc.subject | Endothelin-B receptor | |
| dc.subject | Embryonic mouse gut | |
| dc.subject | Waardenburg-syndrome | |
| dc.subject | Mutation analysis | |
| dc.subject | Gene-expression | |
| dc.subject | Ret receptor | |
| dc.title | Phox2b function in the enteric nervous system is conserved in zebrafish and is sox10-dependent | |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 669 | |
| oaire.citation.issue | 5 | |
| oaire.citation.startPage | 659 | |
| oaire.citation.title | Mechanisms of Development | |
| oaire.citation.volume | 122 | |
| person.familyName | Pinto | |
| person.familyName | Cancela | |
| person.givenName | Jorge | |
| person.givenName | M. Leonor | |
| person.identifier.orcid | 0000-0003-1501-458X | |
| person.identifier.orcid | 0000-0003-3114-6662 | |
| person.identifier.rid | J-7827-2013 | |
| person.identifier.scopus-author-id | 8656187600 | |
| rcaap.rights | openAccess | |
| rcaap.type | article | |
| relation.isAuthorOfPublication | 84f2bfd8-21d5-42f9-ab9b-510e975ce7f1 | |
| relation.isAuthorOfPublication | b9bbfe32-3dfe-4131-ad14-a4394008447f | |
| relation.isAuthorOfPublication.latestForDiscovery | 84f2bfd8-21d5-42f9-ab9b-510e975ce7f1 |
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