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dc.contributor.advisorJaime A. Rivera-Perez, PhD
dc.contributor.authorTortelote, Giovane G.
dc.date2022-08-11T08:08:44.000
dc.date.accessioned2022-08-23T16:06:02Z
dc.date.available2022-08-23T16:06:02Z
dc.date.issued2012-11-06
dc.date.submitted2013-03-27
dc.identifier.doi10.13028/5xx4-8047
dc.identifier.urihttp://hdl.handle.net/20.500.14038/31994
dc.description.abstractThe formation of the anterior-posterior axis requires a symmetry-breaking event that starts gastrulation. Ultimately, the morphogenetic movements of gastrulation reshape the embryo to its final tri-dimensional form. In mouse embryos, the identity of the molecule that breaks the bilateral symmetry and sets in motion gastrulation remains elusive. The Wnt signaling pathway plays a pivotal role during axial specification and gastrulation in metazoans. Loss-of-function experiments have demonstrated a requirement of Wnt3 for gastrulation in mice. But because Wnt3 is expressed sequentially in two tissues, the visceral endoderm and the epiblast, its tissue specific requirements remain uncertain. Here, we report that embryos lacking Wnt3 specifically in the visceral endoderm do not form a primitive streak, mesoderm, endoderm or any derivatives. Visceral endoderm-specific Wnt3 mutants also lack primordial germ cells. Moreover, we provide data demonstrating that Wnt3 carries out its actions in the epiblast via the canonical Wnt pathway. Together, these data suggest that the posterior visceral endoderm via Wnt3, regulates the development of mouse embryos in a similar fashion to the amphibian Nieuwkoop center. Next, we conditionally ablated Wnt3 locus in the epiblast to investigate whether Wnt3 expression is also required in that tissue. Embryos lacking Wnt3 expression in the epiblast, but retaining its expression in the visceral endoderm, show delayed but not absent gastrulation. We conclude that the expression of Wnt3 in the epiblast is required for maintenance but not initiation of gastrulation in mouse embryos. Furthermore, we used in vitro and in vivo approaches to demonstrate that the Wnt3-mediated activation of the canonical Wnt pathway leads to β-catenin occupancy followed by transcription of key loci, including the Wnt3 locus itself, during gastrulation in mice. Our data indicate the presence of an autoregulatory loop in which Wnt3 controls its own expression and orchestrates the process of gastrulation in the mouse embryo.
dc.language.isoen_US
dc.rightsCopyright is held by the author, with all rights reserved.
dc.subjectWnt3 Protein
dc.subjectGastrulation
dc.subjectMice
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectAnimal Experimentation and Research
dc.subjectCell and Developmental Biology
dc.subjectEmbryonic Structures
dc.titleAn Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation
dc.typeDoctoral Dissertation
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1645&context=gsbs_diss&unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_diss/643
dc.legacy.embargo2013-11-15T00:00:00-08:00
dc.identifier.contextkey3965553
refterms.dateFOA2022-08-30T15:12:16Z
html.description.abstract<p>The formation of the anterior-posterior axis requires a symmetry-breaking event that starts gastrulation. Ultimately, the morphogenetic movements of gastrulation reshape the embryo to its final tri-dimensional form. In mouse embryos, the identity of the molecule that breaks the bilateral symmetry and sets in motion gastrulation remains elusive. The Wnt signaling pathway plays a pivotal role during axial specification and gastrulation in metazoans. Loss-of-function experiments have demonstrated a requirement of <em>Wnt3</em> for gastrulation in mice. But because <em>Wnt3</em> is expressed sequentially in two tissues, the visceral endoderm and the epiblast, its tissue specific requirements remain uncertain. Here, we report that embryos lacking <em>Wnt3</em> specifically in the visceral endoderm do not form a primitive streak, mesoderm, endoderm or any derivatives. Visceral endoderm-specific <em>Wnt3 </em>mutants also lack primordial germ cells. Moreover, we provide data demonstrating that <em>Wnt3</em> carries out its actions in the epiblast via the canonical Wnt pathway. Together, these data suggest that the posterior visceral endoderm via <em>Wnt3</em>, regulates the development of mouse embryos in a similar fashion to the amphibian Nieuwkoop center. Next, we conditionally ablated <em>Wnt3</em> locus in the epiblast to investigate whether Wnt3 expression is also required in that tissue. Embryos lacking <em>Wnt3</em> expression in the epiblast, but retaining its expression in the visceral endoderm, show delayed but not absent gastrulation. We conclude that the expression of <em>Wnt3</em> in the epiblast is required for maintenance but not initiation of gastrulation in mouse embryos. Furthermore, we used <em>in vitro</em> and <em>in vivo</em> approaches to demonstrate that the <em>Wnt3</em>-mediated activation of the canonical Wnt pathway leads to β-catenin occupancy followed by transcription of key loci, including the <em>Wnt3</em> locus itself, during gastrulation in mice. Our data indicate the presence of an autoregulatory loop in which <em>Wnt3</em> controls its own expression and orchestrates the process of gastrulation in the mouse embryo.</p>
dc.identifier.submissionpathgsbs_diss/643
dc.contributor.departmentPediatrics
dc.description.thesisprogramCell Biology


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