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dc.identifier.urihttp://hdl.handle.net/11401/76931
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeThesis
dcterms.abstractDuring vertebrate development, formation of the head -to-tail body axis is shaped by a group of unspecified cells at the caudal region of the embryo. The undifferentiated tail bud stem cells are capable of adopting mesodermal or neural cell fates as the embryo develops, but the mechanism of this patterning process remains largely unknown. Our previous studies confirm that Wnt signaling is required in tail bud stem cells to repress the neural transcription factor sox2 and induce mesodermal fate. However, it is unclear if sox2 repression at the cell-autonomous level is the critical factor required for Wnt mediated mesoderm induction. Using zebrafish transgenic lines, we reveal that downregulation of sox2 is necessary for mesodermal progenitors to exit the tail bud. Surprisingly, we also find that ectopic sox2 can induce neural tissue in cells normally destined to give rise to somites in a Wnt signaling-dependent manner. Constitutive expression of Wnt represses sox2 expression and promotes adaption of mesodermal fate, whereas overexpression of sox2 downregulates Wnt pathway activity, inducing neural fate adaption. Moreover, simultaneous high level of Wnt signaling and high level of sox2 promotes the long term bipotential state of tailbud stem cells. Together our results reveal the requirement of precise regulation of differential expression levels of sox2 and Wnt pathway in proper tissue patterning during embryo development.
dcterms.available2017-09-20T16:51:28Z
dcterms.contributorMartin, Benjamin Len_US
dcterms.contributorSirotkin, Howard.en_US
dcterms.creatorTseng, Yu-Jung
dcterms.dateAccepted2017-09-20T16:51:28Z
dcterms.dateSubmitted2017-09-20T16:51:28Z
dcterms.descriptionDepartment of Biochemistry and Cell Biology.en_US
dcterms.extent35 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/11401/76931
dcterms.issued2015-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:51:28Z (GMT). No. of bitstreams: 1 Tseng_grad.sunysb_0771M_12599.pdf: 78093360 bytes, checksum: 1e5d20733ceb02087e3f8fcd8d89f700 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectBiochemistry
dcterms.subjectdevelopment, fate sepcification, sox2, stem cell, Wnt
dcterms.titleThe roles of sox2 and canonical Wnt signaling pathway in fate specification of tailbud bipotential stem cells
dcterms.typeThesis


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