Abstracts - Society for Developmental Biology
Abstracts - Society for Developmental Biology
Abstracts - Society for Developmental Biology
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Program/Abstract # 13<br />
Evolution and development in Lycophytes<br />
Ambrose, Barbara A.; Smalls, Tynisha; Vasco, Alejandra, The New York Botanical Garden, New York, United States<br />
Evolutionary developmental biology studies in lycophytes are integral to our understanding of land plant evolution and<br />
development as the lycophytes occupy a key phylogenetic position within the land plants as sister to all other vascular<br />
plants. In addition, lycophytes have interesting morphological structures, including microphylls, rhizophores and<br />
heterospory, whose evolution and development has been debated <strong>for</strong> more than a century. Compared to the flowering<br />
plants, lycophytes have not only simple sporophyte bodies but also simple genomes. Recent genome sequencing of the<br />
lycophyte, Selaginella moellendorffii, shows that there is no whole genome duplication characterizing this species. We are<br />
cloning and analyzing several key transcription factor families across the lycophytes as well as analyzing the expression of<br />
known key regulators in leaf and reproductive organ development from angiosperms in S. moellendorffii. The Type II<br />
MADS-box genes are well known <strong>for</strong> their role in flower development, and even though there are no orthologs ofthese<br />
floral MADS-box genes in the S.moellendorffii genome, the Selaginella Type II MADS-box genes are expressed in<br />
reproductive structures. Type I MADS box genes play a large role in gametophyte, embryo and seed development and our<br />
analyses suggest that these may be important <strong>for</strong> sporangia development in S. moellendorffii. We have also analyzed the<br />
leaf development network in S. moellendorffii and have found that a large number of the members of this network are<br />
present in the S. moellendorffii genome and are expressed during microphyll development. Our analyses provide insights<br />
into lycophyte evolution and development and highlight the need <strong>for</strong> a functional model system in the lycophytes.<br />
Program/Abstract # 14<br />
Development of a localized nervous system in a dipleurula-type larva.<br />
Yankura, Kristen; Koechlein, Claire; Hughes, Stephanie; Hinman, Veronica Frances, Carnegie<br />
Mellon University, Pittsburgh, United States<br />
The development of centralized nervous systems in many species of arthropods and chordates is extremely well<br />
characterized; however, very little is known about the <strong>for</strong>mation of localized systems of neurons that are present in the vast<br />
diversity of animals. We provide an explanation <strong>for</strong> the development of a localized system of neurons that is associated<br />
with the ciliary bands of the dipleurula-type larvae of seastars. These larvae have two distinct ciliary bands, positioned<br />
above and below the mouth, that extend posteriorly and anteriorly along the dorsal surface and loop back to the ventral<br />
surface. Neurons associated with these bands are there<strong>for</strong>e located at multiple points along the anterior-posterior (AP) and<br />
thedorsal-ventral (DV) axes of the larva, suggesting that they cannot be specified by a simple integration of the AP/DV<br />
signaling system that is common to arthropods and chordates. Rather, we show that conserved Wnt, Nodal and BMP<br />
signaling pathways establish a pro-ciliary band territory that is needed to establish a neurogenic potential “edge” along<br />
which ciliary band associated neurons become specified. This constitutes a novel mechanism <strong>for</strong> neural specification in<br />
animals. We discuss how this mechanism <strong>for</strong> neural patterning contributes to an understanding of the evolution of<br />
centralized nervous systems in chordates.<br />
Program/Abstract # 15<br />
Evolution of development in the amniotes: New insights from genomic studies of somitogenesis in the lizard and<br />
alligator<br />
Eckalbar, Walter L., Arizona State University, Tempe, United States; Elsey, Ruth (Louisiana Dept of Wildlife and<br />
Fisheries); Lasku, Eris (Arizona State U); Allen, April; Corneveaux, Jason (Translational Genomics Res Inst); DeNardo,<br />
Dale; Wilson-Rawls, Jeanne (Arizona State U); Huentelman, Matthew (Translational Genomics Res Inst); Rawls, Alan;<br />
Kusumi, Kenro (Arizona State U)<br />
The segmented spine arises from the developmental process of somitogenesis, which is regulated through the cycling<br />
mechanism termed the ‘segmentation clock’. Major regulatory changes in this developmental clock have been associated<br />
with vertebrate evolution, but our ability to refine this analysis has been limited by major gaps, particular the lack of data<br />
from reptiles. We have extended this comparative analysis to two key reptilian taxa: a squamate, the green anole Anolis<br />
carolinensis, and an archosaurian reptile, the American alligator, Alligator mississippiensis. The newly sequenced<br />
genomes as well as our own deep sequencing of embryonic transcriptomes has provided intriguing data <strong>for</strong> analysis in the<br />
anole and alligator. Further, in situ hybridization was used to localize dynamic expression patterns. This analysis revealed<br />
key changes in segmentation clock gene expression, reflecting convergence and divergence of regulatory mechanisms<br />
within the amniotes. We found that cyclical genes in the clock were particularly divergent. This includes expression of<br />
lunatic fringe, which has cyclical expression in mouse and chicken, but not in the lizard or alligator, as well as delta like 1,<br />
which shares cyclical expression in the anole and mouse. Gradient and determination front components of the segmentation<br />
clock were generally more conserved, with the exception of hes6, which is expressed in a posterio rgradient in anoles, like