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Congress Abstracts - Society for Developmental Biology

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examples whose Shh expression requires additional explanation: snakes and crocodylians. Emerging in situ hybridization data from<br />

the frog Silurana (Xenopus) tropicalis may increase the need to revisit the odontogenic band, as it provides the first tooth gene<br />

expression data <strong>for</strong> any amphibian taxon. I present a developmental series of S. tropicalis prometamorphic tadpoles (Nieuwkoop and<br />

Faber stages 55-58), the time period encompassing the odontogenesis of first-generation teeth. This series presents an important<br />

comparative datapoint in representing a vertebrate whose life history has been modified to include an extended, specialized, and<br />

toothless larval stage. I evaluate these comparative data from an evolutionary perspective, identifying phenotypes which indicate that<br />

developmental mechanisms <strong>for</strong> tooth competence, tooth initiation, and mouth <strong>for</strong>mation may be decoupled in developmental time.<br />

Program/Abstract # 294<br />

Endless pigeons most colorful: genetics and development of feather pigment diversity among domestic rock pigeons<br />

Domyan, Eric; Kronenberg, Zev; Guernsey, Michael; Vickrey, Anna; Cassidy, Pamela; Shapiro, Michael (University of Utah, USA)<br />

Centuries of selective breeding have crafted tremendous phenotypic diversity among breeds of domestic rock pigeon (Columba livia),<br />

providing a rich model to investigate the process of phenotypic variation. To understand the genetic basis of this diversity, we recently<br />

sequenced and interrogated the genomes of 40 pigeons from breeds with distinct sets of derived traits. Here we present the preliminary<br />

identification of several mutations underlying color variation within and among pigeon breeds. Interestingly, one non-synonymous<br />

mutation associated with ash-red feather color is located in the Tyrosinase-related protein 1 (Tyrp1) gene. This dominant mutation<br />

reduces the efficiency of signal peptide cleavage. In addition, we identify putative null alleles of this gene that act recessively to cause<br />

brown feather color; there<strong>for</strong>e, the dominant ash-red allele may represent a neomorphic allele. Tyrp1 is thus a strong candidate <strong>for</strong> the<br />

blue/ash-red/brown locus of classical pigeon genetics. We also identify a mutant allele of Slc45a2 that is associated with a reduction<br />

in feather pigmentation and is a strong candidate <strong>for</strong> the dilute locus of classical pigeon genetics. By determining the genotype of birds<br />

at these two loci, we are able to explain some of the most common feather colors among domestic pigeons.<br />

Program/Abstract # 295<br />

<strong>Developmental</strong> basis of phallus reduction during bird evolution<br />

Herrera, Ana M; Shuster, Simone (University of Florida, USA); Perriton, Claire (University of Reading, UK); Cohn, Martin (Howard<br />

Hughes Medical Institute, USA)<br />

One of the most puzzling events in evolution is the loss of the phallus in birds. All birds reproduce by internal fertilization, but only<br />

~3% of birds have retained a phallus capable of intromission. Behavioral studies have implicated sexual selection as the evolutionary<br />

mechanism responsible <strong>for</strong> phallus reduction; however, the underlying developmental mechanism is unknown. We investigated<br />

external genital development in two sister clades, Galli<strong>for</strong>mes (land fowl), which lack an intromittent phallus, and Anseri<strong>for</strong>mes<br />

(waterfowl), which have well developed phalluses, as well as two out groups, Paleognathae (emus) and Crocodilia (alligators).<br />

Galli<strong>for</strong>m embryos undergo cryptic development of a genital tubercle, but later this undergoes apoptosis and regresses. A derived<br />

pattern of Bmp4 expression was identified in galli<strong>for</strong>m genital tubercles. Functional experiments show that Bmp activity is necessary<br />

and sufficient <strong>for</strong> apoptosis and regression of the genital tubercle. Our results suggest that evolutionary acquisition of a novel Bmp4<br />

domain in the distal genital tubercle underlies loss of an intromittent phallus in galli<strong>for</strong>ms.<br />

Program/Abstract # 296<br />

The evolution of external genitalia: sexual reproduction on dry land<br />

Tschopp, Patrick; Sherratt, Emma; Sanger, Thomas; Groner, Anna; Aspiras, Ariel (Harvard U., USA); Pourquie, Olivier (Strasbourg<br />

Univ. Medical School, France); Gros, Jerome (Institut Pasteur, France); Tabin, Clif<strong>for</strong>d (Harvard U.,USA)<br />

The appearance of internal fertilization has been considered a major step in the emergence of terrestrial vertebrates. In mammals, the<br />

molecular pathways driving the outgrowth of the genital bud highly resemble those that are active during limb development. Here, we<br />

provide a potential explanation <strong>for</strong> these observed similarities: we show that in squamates (lizards and snakes), the external genitalia<br />

develop as a direct outgrowth of the limb bud, or the remnants thereof. CT scan analyses reveal a relative repositioning of the cloaca,<br />

an important signaling center during genitalia development, towards the limb field in all squamates investigated. Lentiviral lineage<br />

tracing using a novel ex ovo culturing system in anole lizards shows that limb and genitalia share a common embryonic origin in this<br />

species, coming from the lateral plate mesoderm. In contrast, mouse and chicken genital buds seem to originate from the tail bud.<br />

Comparative RNA-seq analysis of embryonic tissues corroborates this notion, showing more similar molecular fingerprints <strong>for</strong> the<br />

anole genital and limb buds, as opposed to their mouse counterparts. Finally, the importance of cloaca position underlying this<br />

genitalia shift is suggested by a series grafting experiments in chicken and mouse. The transplantation of cloacal tissue into the early<br />

limb bud leads to tissue outgrowth and ectopic activation of genes normally associated with genital bud development. We speculate<br />

that the recruitment of a mesenchymal cell population, namely the early limb bud, by the cloacal signaling center might initially have<br />

fostered the emergence of external genitalia, preserving key ancestral gene circuitries thereafter, regardless of subsequent<br />

repositioning.<br />

Program/Abstract # 297<br />

Moleculars mechanism control cytoskeletal activities during inner ear invagination<br />

Sai, Xiaorei (Riken CDB, Japan)<br />

85

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