Authors

Yu-Jung Tseng

Type

Text

Type

Thesis

Advisor

Sirotkin, Howard. | Martin, Benjamin L

Date

2015-12-01

Keywords

Biochemistry | development, fate sepcification, sox2, stem cell, Wnt

Department

Department of Biochemistry and Cell Biology.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/76931

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

During 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. | 35 pages

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