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University of Houston

Function and Regulation of the Conserved Wnt Target sp5 in the Vertebrate Nervous System

Abstract

dc:description.abstract

Wnt/β-catenin signaling culminates in the transcriptional regulation of target genes. Target genes mediate Wnt function during different developmental processes. A dysfunctional Wnt/β-catenin signaling results in aberrant regulation of the target genes that often causes developmental malformations and cancer. In order to understand how Wnt signaling regulates development and diseases, identification of its downstream network of transcriptional targets and their subsequent roles is required. sp5 gene is a target of Wnt signaling in several vertebrates and invertebrates including humans, Xenopus, Mouse, zebrafish, Hydra and amphioxus. Despite the evidence of its involvement in Wnt mediated processes in several species, its regulation and exact function during Wnt mediated nervous system patterning is not well studied. Here we show that during neural patterning, Wnt/β-catenin signaling regulates the transcription of 3 Sp-family genes in zebrafish: sp5a, sp5-like (sp5l) and sp8b. These 3 genes are expressed in the neural plate during embryogenesis. I generated single and double loss of function genetic mutants for sp5a and sp5l that do not exhibit any observable phenotypic defects during development. However, sp5a, sp5l and sp8b triple knockdown embryos display hindbrain and posterior body defects, indicating that sp8b acts redundantly with the sp5a and sp5l to regulate early development and patterning. I examined the regulation of sp5a by Wnt and FGF in transgenic reporter lines to show that the promoter of sp5a is responsive to modulation in Wnt and FGF signaling levels. De-repression by Wnt followed by activation by FGF signaling is required for the expression of sp5a in the neural plate during embryonic development. Furthermore, I showed that sp5a is expressed in the adult habenula and regulates the expression of the habenular progenitor marker gene dbx1b. RNA sequencing reveals significant downregulation of dbx1b in sp5a loss of function mutants. Comparison of wild-type and mutant sp5a reporter lines suggests that the sp5a expression in the habenula is regulated by Wnt signaling. This data suggests a potential role of sp5a in habenula neurogenesis, downstream of Wnt signaling, through the regulation of dbx1b.

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy
Level thesis:degree_level
Doctoral
Discipline thesis:degree_discipline
Biology
Grantor
University of Houston
Year dc:date.issued
2023

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mohanty, Saurav
Advisor dc:contributor.advisor
  • Lekven, Arne C.
Committee members dc:contributor.committeemember
  • Alward, Beau A.
  • Dauwalder, Brigitte
  • Lin, Chin-Yo

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • The author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/10657/16192
OAI identifier oai:identifier
oai:uh-ir.tdl.org:10657/16192

Chain of custody

source
Harvested from
University of Houston
Base URL
uh-ir.tdl.org/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Mohanty, Saurav. Function and Regulation of the Conserved Wnt Target sp5 in the Vertebrate Nervous System. Doctoral thesis, University of Houston, 2023. https://hdl.handle.net/10657/16192