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Abstracts - Society for Developmental Biology

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doses led to inhibition in cell movements while a percentage of the embryos showed abnormal tissue separation. These<br />

observations suggest that, in addition to its potential teratogenic effect on head development, retinoic acid has also a<br />

positive regulatory role in head induction during early gastrula. This novel activity ofretinoic acid signaling is in agreement<br />

with the proposed reduction of this signal in syndromes exhibiting craniofacial mal<strong>for</strong>mations.<br />

Program/Abstract # 345<br />

The role of maternal Dpp/BMP pathway in the early Drosophila embryo.<br />

Fontenele, Marcio; Pentagna, Nathalia; Araujo, Helena, Federal University of Rio de Janeiro, Brazil<br />

Dorsoventral (DV) patterning in Drosophila melanogaster is regulated by the Toll pathway by modulating Cactus/IkB<br />

protein degradation, and thus nuclear Dorsal/NFkB protein levels in the early embryo. In addition to the Toll pathway,<br />

through previous genetic and biochemical studies we have shown that the maternal Dpp/BMP pathway regulates nuclear<br />

Dorsal levels by controlling Toll-independent degradation of Cactus. The maternal Dpp pathway requires Calpain A, a<br />

calcium-activatedcysteine protease, to target Cactus degradation and thus to regulate Dorsal levels. Using a Real-time<br />

qPCR approach we have shown that the maternal Dpp pathway regulates mRNA levels of CalpainA and Casein Kinase II<br />

in the earlyembryo. These results suggest that maternal Dpp functions through a novel mechanism, since the effects of Dpp<br />

blockage are observed be<strong>for</strong>e the onset of zygotic transcription. This raises the possibility that the maternal Dpp/BMP<br />

pathway acts through post-transcriptional mechanisms to regulate stability or degradation of mRNAs. Accordingly, null<br />

germline clones <strong>for</strong> the tkv type I receptor, mad or medea SMADs generate DV patterning defects similar to those reported<br />

<strong>for</strong> blockage of the tkvreceptor. In order to define the functional role of maternal Dpp on mRNA levels we have<br />

undertaken a qPCR approach. Recent data reveals that we are able to detect variations in mRNA levels in the preblastoderm<br />

embryo upon blockage of maternal Dpp signals. The results obtained up to now suggest that Dpp regulates<br />

maternal mRNA levels in the embryo. We are currently exploring whether some of these maternal mRNAs participate with<br />

Dpp to regulate discrete nuclear Dorsal levels and thus DV patterning. This work is supported by CNPq, Pronex, FAPERJ<br />

and INCT-EM.<br />

Program/Abstract # 346<br />

Split top: A maternal regulator of dorsal-ventral patterning and cell migration in zebrafish<br />

Langdon, Yvette G., University of Pennsylvania Cell and Development, Philadelphia, United States; Gupta, Tripti<br />

(Cambridge, United States); Marlow, Florence (Bronx, United States); Abrams, Elliott (Philadelphia, United States);<br />

Mullins, Mary (Philadelphia, United States)<br />

Maternal factors are required <strong>for</strong> many early developmental processes including fertilization, egg activation, and <strong>for</strong>mation<br />

of the body axes during embryonic development of the zebrafish, Danio rerio. Our lab has per<strong>for</strong>med a recessive maternaleffect<br />

mutagenesis screen and identified a number of mutants with defects in early developmental processes, including<br />

early morphogenesis and body axis <strong>for</strong>mation. One such mutant, Split top exhibits abnormal dorsal-ventral patterning,<br />

displaying a dorsalization of the embryonic axis. Clutches of embryos from Split top mutant mothers are characterized by<br />

the five classic dorsalized phenotypic classes, as well as some additional defects. The mutant embryos show an expansion<br />

of dorsal markers and a corresponding reduction in ventral markers during gastrulation indicative of dorsalization. The<br />

additional defects appear to be the result of altered morphogenesis, including defects in epiboly, the process by which the<br />

blastoderm cells migrate over and surround the yolk. Split top mutant embryos also appear to be defective in the cell<br />

movement process of convergence and extension. We mapped the Split top mutation to chromosome 17, within a 1 MB<br />

interval and ef<strong>for</strong>ts are currently underway to positionally clone the affected gene.<br />

Program/Abstract # 347<br />

Oocyte asymmetry and the animal-vegetal axis in zebrafish<br />

Marlow, Florence; Heim, Amanda; Rothhamel, Sophie; Hartung, Odelya; Schwartz-Orbach, Lianna; Jenny, Andreas,<br />

Albert Einstein College of Medicine, New York, United States<br />

The vertebrate animal-vegetal axis is established during oogenesis. Oocyte polarity is pre-requisite <strong>for</strong> determining the<br />

prospective embryonic axes and setting aside the germ cell determinants in non-mammalian vertebrates. The Balbiani body<br />

is an evolutionarily conserved oocyte asymmetry present in early oocytes of allanimals examined, including humans.<br />

However, bucky ball is the only gene known to be essential to establish oocyte polarity in vertebrates. Lack of maternal<br />

Buckyball causes failure to specify oocyte asymmetry and the embryonic axes through an unknown pathway and<br />

mechanism. To investigate how Bucky ball regulates asymmetries in oocytes we are testing the hypothesis that buc<br />

specifies the oocyte axis upstream or at the level of Balbiani body assembly. We have identified candidate components of<br />

the Buc pathway through yeast genetic and affinity purification approaches. To identify regions of Buc protein with<br />

potential functional significance we have mapped the regions of the Buc protein that mediate interactions with its binding

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