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Congress Abstracts - Society for Developmental Biology

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works in concert with basal cues from the surrounding tissues <strong>for</strong> the correct spatial assembly of apical junctions and subsequent<br />

lumen <strong>for</strong>mation.<br />

Program/Abstract # 225<br />

Developing a Staging Scheme <strong>for</strong> Monodelphis domestica embryos<br />

Nellett, Kolleen, (Oberlin College, USA); Morrison, Jeremy (Greensburg, PA, USA); Cruz, Yolanda P. (Oberlin College Sci Ctr, USA)<br />

The laboratory opossum, Monodelphis domestica, is the only marsupial maintained in laboratory colonies <strong>for</strong> biological studies that<br />

range from behavioral to genetic. The 2007 sequencing of its genome has enhanced the usefulness of this mammal in investigating<br />

the molecular basis of many developmental events routinely precluded by the extensive embryo-maternal tissue contact that occurs<br />

during implantation in eutherian mammals. Such events, especially organogenesis-related, occur at an exceedingly rapid pace during<br />

the last third of pregnancy—so much so that between days 10 and 11, <strong>for</strong> example, a litter of 14 opossum embryos could consist of<br />

individuals with somite numbers ranging from as few as 6 to as many as 28. We thus sought to devise a staging scheme based on the<br />

appearance of landmark anatomical structures (somites, optic and olfactory vesicles, etc.), rather than pregnancy days elapsed, to make<br />

meaningful comparisons with other vertebrate systems possible. Our results reveal the extent to which organogenetic events appear to<br />

be disordered, relative to those in mouse, chick or human embryo (<strong>for</strong> example, development of <strong>for</strong>elimbs, oral structures, and brain<br />

ventricles is precocious). These results will be useful <strong>for</strong> comparative studies involving organogenesis in these amniotes.<br />

Program/Abstract # 226<br />

PIAS-like protein Zimp7 participates in the Nodal signaling pathway during dorsal mesoderm development in zebrafish<br />

Moreno, Roberto; Schnabel, Denhí; Salas, Enrique; Lomelí, Hilda (National Autonomous University of Mexico, Mexico)<br />

Human ZIMP7 protein and its homolog ZIMP10 were initially identified as androgen receptor co-activators. Analysis of their<br />

sequence revealed the presence of an SP-RING/Miz domain, which is highly conserved in members of the PIAS family and confers<br />

SUMO-conjugating activity. The human ZIMP proteins also interact with transcription factors such as p53 or Smad3/Smad4 and with<br />

BRG1, the catalytic subunit of the SWI-SNF remodeling complex. Accordingly, the drosophila orthologue of the Zimp genes tonalli,<br />

was shown to interact with subunits of the Brahma complex. Mutations in tonalli produce flies with homeotic phenotypes. In zebrafish<br />

zimp7 is ubiquitously expressed in embryos from one-cell up to 24 hpf. In this study we set out to analyze the role of zygotic Zimp7<br />

in the early stages of zebrafish development. We found evidence indicating that Zimp7 is required <strong>for</strong> dorsal mesoderm development.<br />

At 24 hpf, morpholino-mediated reduction of zygotic Zimp7 produced axial mesoderm defects -e.g. floor plate, precordal plate and<br />

notocord- alterations. These defects were accompanied by an up-regulation of nodal-related genes at gastrulation such as squint, no<br />

tail and floating head. Consistently, embryos over-expressing zimp7 RNA exhibited axial defects resembling those ones observed in<br />

squint mutants, like <strong>for</strong>ebrain loss and cyclopia and down-regulation of nodal-related genes. Altogether our results indicate that Zimp7<br />

might be interacting with the nodal-signaling pathway during mesoderm induction.<br />

Program/Abstract # 227<br />

Notochord vacuoles are lysosome-related organelles that function in embryonic axis elongation and spine morphogenesis<br />

Ellis, Kathryn Leigh; Bagwell, Jennifer; Bagnat, Michel (Duke University, USA)<br />

The notochord plays critical structural and signaling roles during vertebrate development. At the center of the vertebrate notochord is a<br />

large fluid-filled organelle, the notochord vacuole. While these highly conserved intracellular structures have been described <strong>for</strong><br />

decades, little is known about the molecular mechanisms involved in their biogenesis and maintenance. Here we show that zebrafish<br />

notochord vacuoles are specialized post-Golgi structures and a new type of lysosome-related organelle. Through the use of dominant<br />

negatives, mutants, and pharmacological inhibitors we show that vacuole <strong>for</strong>mation and maintenance requires late endosomal<br />

trafficking regulated by the vacuole-specific Rab32a and H + -ATPase-dependent acidification. We establish that notochord vacuoles<br />

are required <strong>for</strong> body axis elongation during embryonic development and identify a novel role <strong>for</strong> notochord vacuoles in spine<br />

morphogenesis. Thus, the vertebrate notochord plays important structural roles beyond early development. We are currently using live<br />

imaging to further understand how the notochord acts as a hydrostatic scaffold during vertebrae <strong>for</strong>mation. These experiments will<br />

provide insights into the cellular mechanisms behind congenital scoliosis.<br />

Program/Abstract # 228<br />

Cdx and Hox genes, and body axis extension of the mouse embryo<br />

Neijts, Roel; Monteiro, Ana-Rita; van Rooijen, Carina; Deschamps, Jacqueline (Hubrecht Institute and UMC Utrecht, Netherlands)<br />

Mouse Cdx and Hox genes are involved in regulating the posterior elongation of axial tissues that they will subsequently pattern. They<br />

work by maintaining active growth signaling in the embryonic growth zone. Cdx mutations cause axial truncation of varying severity<br />

depending on the identity and number of invalidated alleles. The Hox genes also participate in axial growth, in a way obeying spatiotemporal<br />

colinearity. While central Hox genes can replace Cdx genes in their axial growth promoting function, expression of<br />

posteriormost Hox genes must obligatorily remain silent until later embryonic stages. We will present data documenting the<br />

differential functional capacity of 3’ to 5’ Hox genes in modulating axial growth, exposing the relationship between Cdx and Hox<br />

genes.<br />

Program/Abstract # 229<br />

Withdrawn<br />

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