Abstracts - Society for Developmental Biology
Abstracts - Society for Developmental Biology
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