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Congress Abstracts - Society for Developmental Biology

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The inner ear contains the sensory organs <strong>for</strong> the hearing and balancing and is embedded within the cephalic mesoderm of the embryo.<br />

However it is induced by fibroblast growth factor signals as an epithelial placode in the surface ectoderm adjacent to the posterior<br />

hindbrain. In the chick, the inner ear placode first becomes morphologically apparent as a thickening of the ectoderm. It then gradually<br />

invaginates to <strong>for</strong>m an otocyst within the head mesenchyme. We have previously showed that basal fibroblast growth factor (FGF)<br />

signalling acting through phospholipase Cγ activates basal myosin II. Myosin II exhibits a non-canonical activity that results in the<br />

local depletion of actin filaments and thus causes the basal expansion of the otic placode. Subsequent to basal expansion of the inner<br />

ear placode, apical constriction drives to complete invagination. We find that the small GTPase protein, RhoA is localized apically and<br />

activation of RhoA increases gradually during inner ear morphogenesis. Our data provide evidence that RhoA play bi-functional roles<br />

to trigger apical constriction of the otic epithelia and likely, this is FGF independent process. Firstly, RhoA regulates the assembly of<br />

junctional actin filaments. Secondly, RhoA controls the apical activation of myosin light chain, the active component of Myosin II. I<br />

describe the detail molecular pathway involved in RhoA-coordinated apical constriction during otic morphogenesis.<br />

Program/Abstract # 298<br />

Convergent evolution of cellular immunity in jawless fish<br />

McCurley, Nathanael; Guo, Peng; Cooper, Max (Emory University, USA)<br />

Adaptive immune reactions require a complex choreography of molecules, cells, and tissues, yet this <strong>for</strong>m of immunity appeared<br />

suddenly in evolution with the emergence of the vertebrates. The jawless vertebrates (lampreys and hagfish), however, lack the key<br />

antigen receptor genes that mediate adaptive immunity in the jawed vertebrate lineage. Instead, jawless vertebrates use a novel gene<br />

family encoding leucine-rich repeat proteins that are somatically diversified, monoallelically expressed on lymphocytes, and used as<br />

antigen receptors in adaptive immune reactions. These variable lymphocyte receptors (VLRs) are generated during lymphocyte<br />

development by a stochastic gene assembly process resulting in a potential antigen receptor repertoire of >10 14 . Our lab identified a<br />

VLR lymphocyte population in lampreys (termed VLRA cells) that resembles the T cells of jawed vertebrates by numerous<br />

parameters that include development in the recently characterized lamprey thymus equivalent. The nature of the antigen recognized by<br />

VLRA receptors remains unknown, though current data suggest that they bind processed antigens. We hypothesize that VLRA cells<br />

are involved in cellular immune responses, possibly through recognition of antigen presented in the context of histocompatibility<br />

determinants. We devised several experimental approaches to test this hypothesis and our data indicate that VLRA cells respond<br />

preferentially to allogeneic stimulation, suggesting a role in cellular immunity. We furthermore used allogeneic immunization to<br />

develop antisera that recognize lamprey allodeterminants on myeloid leukocytes, consistent with the hypothesis that these cells<br />

express the antigen that drives allogeneic responses.<br />

Program/Abstract # 299<br />

Comparative analysis of the colon in the vertebrate lineage.<br />

Theodosiou, Nicole; Wechter, Todd; Jain, Meaghan (Union College, USA)<br />

During the aquatic to terrestrial transition, vertebrates were challenged by dehydration once on land. The development of a colon<br />

allowed tetrapods to maintain water homeostasis and prevent desiccation. In contrast to beliefs that a colon evolved after tetrapod<br />

evolution, a rudimentary colon exists in the cartilaginous fish Leucoraja erinacea (skate) and Squalus acanthias (dogfish). This is<br />

surprising because elasmobranchs appeared 450 mya, and thus predate the transition from aquatic to terrestrial life (approximately 370<br />

mya). To understand if elasmobranchs were pre-adapted <strong>for</strong> conserving water prior to the tetrapod transition, the digestive tracts of<br />

representative species from gnathostomes and ray-finned fish are being examined <strong>for</strong> colon developmental markers and histology. The<br />

lamprey Petromyzon marinus contains a discreet region in the distal intestine with elevated levels of acid mucin-producing goblet<br />

cells, cell markers <strong>for</strong> the colon. A similar region with colon-like cells is found in the distal intestine of the ray-finned fish Polyodon.<br />

In addition, there is a dorsal-ventral asymmetry to the acid mucin distribution in the lamprey and paddlefish. The dorsal-ventral<br />

asymmetry in lamprey and paddlefish suggests a common origin <strong>for</strong> the colon in vertebrates. However, the asymmetry is not observed<br />

in different species of elasmobranchs suggesting that a rudimentary colon may have been advantageous to elasmobranchs, allowing<br />

them to adapt to different environments with changing salinities. Together these data suggest that the colon arose prior to the tetrapod<br />

transition and expanded in the vertebrate lineage.<br />

Program/Abstract # 300<br />

The role of lbx1 during Xenopus and Nematostella embryogenesis – a comparative study of myogenesis in metazoans<br />

Strobl, Anna-Christina (NIMR MRC, UK) Steinmetz, Partick; Fredman, David; Technau, Ulrich (University of Vienna, Austria);<br />

Smith, Jim (NIMR MRC, UK)<br />

In vertebrates, one of the main tissues derived from the mesodermal germ layer is muscle. The early branching metazoans, however,<br />

lack mesoderm, and their muscle derives from the endoderm. We are studying the evolutionary relationship between cnidarian and<br />

vertebrate myogenesis to improve our understanding of the mechanisms regulating muscle development. Although the cnidarian<br />

Nematostella vectensis does not possess mesoderm, many ‘mesodermal’ transcription factors are encoded in its genome. We dissected<br />

the function of one such gene, the NK-homeobox transcription factor ladybird (lbx1), which is involved in muscle <strong>for</strong>mation in both<br />

Nematostella and Xenopus. Morpholino-mediated knockdown of Nvlbx1 results in changes of endodermal morphology, probably due<br />

to loss of mesenteric muscle cells. This indicates that Nvlbx1 regulates endoderm differentiation and in particular muscle <strong>for</strong>mation in<br />

Nematostella. By using RNA-Seq to identify genes that are up- or downregulated in Nematostella Nvlbx1 morphants, we have gained<br />

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