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dc.contributor.authorMcDonald, Lindsay
dc.date.accessioned2011-12-19T16:31:58Z
dc.date.available2011-12-19T16:31:58Z
dc.date.issued2011-12-19
dc.identifier.urihttp://hdl.handle.net/10222/14384
dc.description.abstractHACE1 is a tumour suppressor gene located at human chromosome 6q21. HACE1 is downregulated in Wilms’ tumour as well as several other human cancers. Its role in normal development remains unknown. The zebrafish has established itself as a robust model for studying vertebrate development and human cancers. A zebrafish hace1 homologue has been identified. Whole mount in situ hybridization (WISH) assays and colocalization studies demonstrate conserved hace1 expression. Moreover, morpholino knockdown of hace1 reveals perturbed cardiac development and function. Transgenic zebrafish harboring either wild type or dominant negative mutated C876S (C876S DN) human HACE1 genes have been generated. DN zebrafish display increased apoptosis, both untreated and following irradiation-induced cellular damage. There was no difference in cell cycle progression between wild type embryos and C876S DN. Further characterization of the HACE1 transgenic zebrafish model will serve to better our understanding of the role of human HACE1 in normal development and tumourigenesis.en_US
dc.language.isoenen_US
dc.subjectCanceren_US
dc.subjectZebrafishen_US
dc.subjectTumour suppressoren_US
dc.subjectWilms' tumouren_US
dc.titleUSING THE ZEBRAFISH MODEL TO DETERMINE THE ROLE OF THE HACE1 TUMOUR SUPPRESSOR IN NORMAL DEVELOPMENT AND TUMOURIGENESISen_US
dc.date.defence2011-06-27
dc.contributor.departmentMedical Sciencesen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinerDr. James Fawcetten_US
dc.contributor.graduate-coordinatorDr. Tim Leeen_US
dc.contributor.thesis-readerDr. Craig McCormicken_US
dc.contributor.thesis-readerDr. David Hoskinen_US
dc.contributor.thesis-readerDr. Mark Walshen_US
dc.contributor.thesis-supervisorDr. Jason Bermanen_US
dc.contributor.ethics-approvalReceiveden_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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