Abstracts - Society for Developmental Biology
Abstracts - Society for Developmental Biology
Abstracts - Society for Developmental Biology
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embryonic precursors to <strong>for</strong>m an alternative cell type. For translational medicine it introduces a new possible source of<br />
cardiomyocytes, derived from an adult tissue, which might be used <strong>for</strong> drug testing or <strong>for</strong> therapeutic transplantation.<br />
Program/Abstract # 427<br />
Specification of the ascidian larval PNS<br />
Zeller, Robert W.; Chen, Jerry; Tang, Joyce ( San Diego State University, United States)<br />
The ascidian larval peripheral nervous system (PNS) consists of a series of paired sensory neurons, called epidermal<br />
sensory neurons (ESNs) that run along the midline of the larva. Other laboratories have shown that both BMP and FGF<br />
signaling are required <strong>for</strong> the early specification of these cells and that the pattern of ESNs is further refined by Notch-<br />
Delta signaling. Here we show that the entire larval epidermis is neurogenic and can be converted into ESNs by the<br />
expression of the single ascidian Pou4 class transcription factor. In the context of a larger gene regulatory network (GRN)<br />
<strong>for</strong> the larval PNS, we have identified at least four microRNAs and at least four transcription factors that operate<br />
downstream of Notch-Delta signaling to pattern the larval ESNs. In Ciona intestinalis, the microRNA miR-124 is<br />
expressed in both the PNS and central nervous systems. We computationally identified miR-124 targets and show that key<br />
miR-124 targets include the Notch receptor, the three HES family genes that mediate Notch signaling and neutralized,<br />
which regulates Delta levels. We show that miR-124 feeds back on Notch-Delta signaling and plays a role in ESN<br />
specification. In addition to Pou4, we have identified at least three additional transcription factors that pattern the ESNs.<br />
By analyzing a matrix of gene expression patterns in transgenic embryos ectopically expressing these transcription factors<br />
we have established a temporal and spatial cascade of regulatory gene expression in the PNS. Interestingly, the<br />
microRNAs and transcription factors we have identified play roles in the specification in the hair cells of the vertebrate<br />
inner ear.<br />
Program/Abstract # 428<br />
Requirements <strong>for</strong> posterior growth in sequentially segmenting arthropods<br />
Nagy, Lisa M.; Nakamoto, Ayaki; Ettling, Alexandria; Harrison, Christy (University of Arizona, Tucson, AZ, United<br />
States); Kim, S.; Lazo del la Vega, Lorena; Tewksbury, Austin; Wambaa, Sam; Williams, Terri (University of Connecticut,<br />
Hart<strong>for</strong>d, United States)<br />
A key feature of the arthropod body plan is the presence of segments along the body axis. Evolution of segments has<br />
permitted broad diversification of arthropods. Most arthropods develop their segments in the same fashion: they add them<br />
one by one from the posterior in a region commonly called the “growth zone”. Although this is the most common mode of<br />
arthropod segmentation, the growth zone is mostly unstudied. We are studying the growth zone at the cellular level in two<br />
groups within the Pancrustacea, crustaceans: the branchiopod Artemia and Thamnocephalus and an insect: the beetle,<br />
Tribolium. Both exhibit features likely ancestral <strong>for</strong> their respective lineages: larval addition of segments in the<br />
branchiopods and sequential addition of segments in the beetle embryo. Recently, a common set of genes - caudal, evenskipped<br />
and Wnts – have been hypothesized to control the growth zone in diverse arthropods. We have characterized the<br />
dimensions of the growth zone and analyzed the behavior of cells relative to the dynamic patterns of gene expression in the<br />
posterior of the developing larvae and germ band. We are also completing a fate map of the blastoderm by tracing the fates<br />
of small clusters of cells subsequent to activation of a photo activatable dye. Our results provide evidence <strong>for</strong> divergent<br />
modes of sequential segmentation in branchiopods and beetles: in the branchiopod posterior growth contributes<br />
continuously to the segmentation process, whereas posterior growth makes a discontinuous contribution to the<br />
segmentation of the Tribolium germ band.<br />
Program/Abstract # 429<br />
A genetic circuit conferring robustness to dorsal patterning in Drosophila<br />
Gavin-Smyth, Jackie; Ferguson, Chip, University of Chicago Ecology and Evolution, Chicago, United States<br />
The robust and invariant development of the wild-type organism is widely thought to be adaptive and essential. Using<br />
quantitative analyses of dorsal patterning in the Drosophila embryo we have assessed the robustness of this event and<br />
determined the genetic mechanism required <strong>for</strong> invariance of wild type patterning. The DV axis of both arthropods and<br />
vertebrates is patterned by the activity of Bone Morphogenetic Protein (BMP) signaling. In D. melanogaster the BMP<br />
ligand Decapentaplegic (Dpp) is essential <strong>for</strong> the specification of dorsal fates in the pre-gastrular embryo. During<br />
cellularization, Dpp signaling is initially localized in a low intensity, broad dorsal domain due to the activity of<br />
extracellular ligand binding proteins. At the onset of gastrulation, the Dpp signaling domain is intensified and refined into<br />
a sharp stripe on the dorsal midline. Previous work indicated that positive feedback was required <strong>for</strong> the <strong>for</strong>mation of this<br />
final signaling domain. Our current work characterizes and defines a component of the feedback circuit, and its interaction<br />
with a BMP signaling antagonist. We find that the combined activity of positive and negative factors leads to the