Gill dimensions in near-term embryos of Amazonian freshwater stingrays (Elasmobranchii: Potamotrygonidae) and their relationship to the lifestyle and habitat of neonatal pups

This comparative study of gill morphometrics in near-term embryos of freshwater stingray potamotrygonids examines gill dimensions in relation to neonatal lifestyle and habitat. In embryos of the potamotrygonids Paratrygon aiereba, Plesiotrygon iwamae, Potamotrygon motoro, Potamotrygon orbignyi, and cururu ray Potamotrygon sp. the number and length of filaments, total gill surface area, mass-specific surface area, water-blood diffusion distance, and anatomical diffusion factor were analysed. In all potamotrygonids, the 3rd branchial arch possessed a larger respiratory surface than the other gill arches. Larger embryos had more gill surface area and large spiracles, which are necessary to maintain the high oxygen uptake needed due to their larger body size. However, the higher mass-specific gill surface area observed in near-term embryos may be advantageous because neonates can use hypoxic environments as refuges against predators, as well as catch small prey that inhabit the same environment. As expected from their benthic mode of life, freshwater stingrays are sluggish animals compared to pelagic fishes. However, based on gill respiratory morphometry (such as gill area, mass-specific gill area, the water-blood diffusion barrier, anatomical diffusion factor, and relative opening of the spiracle), subtypes of lifestyles can be observed corresponding to: active, intermediate, and sluggish species according to Gray's scale.

Este estudo realizado com embriões a termo de arraias de água doce (Potamotrygonidae) compara e analisa as dimensões branquiais em relação ao estilo de vida e habitat dos neonatos. Nos embriões de Paratrygon aiereba, Plesiotrygon iwamae, Potamotrygon motoro, Potamotrygon orbignyi e Potamotrygon sp. (arraia cururu) foram analisados número e comprimento dos filamentos, área branquial, área superficial branquial massa-específica, barreira de difusão água-sangue e fator de difusão anatômico. Em todos os potamotrigonídeos estudados, o 3º arco branquial possui uma superfície respiratória maior que os demais arcos. Embriões de espécies de maior porte possuem grandes espiráculos e maior área de superfície branquial. Isso ajuda a manter a taxa de absorção de oxigênio proporcional ao requerimento do animal. No entanto, a grande área de superfície branquial massa-específica observadas nos embriões a termo pode ser vantajosa, pois os neonatos podem usar ambientes hipóxicos como refúgios contra predadores, bem como capturar pequenas presas que habitam o mesmo ambiente. Devido ao modo de vida bentônico, as arraias de água doce são nadadoras lentas comparadas aos peixes pelágicos. No entanto, com base na morfometria branquial (área de superfície branquial, área branquial massa-específica, barreira de difusão água-sangue, fator de difusão anatômico e abertura relativa do espiráculo), subtipos de estilos de vida podem ser observados: ativas, intermediárias e lentas, conforme escala definida por Gray.

Wdr12, a mouse gene encoding a novel WD-Repeat Protein with a notchless-like amino-terminal domain.

The WD-repeat protein family consists of a large group of structurally related yet functionally diverse proteins found predominantly in eukaryotic cells. These factors contain several (4-16) copies of a recognizable amino-acid sequence motif (the WD unit) thought to be organized into a "propeller-like" structure involved in protein-protein regulatory interactions. Here, we report the cloning of a mouse cDNA, referred to as Wdr12, which encodes a novel WD-repeat protein of 423 amino acids. The WDR12 protein was predicted to contain seven WD units and a nuclear localization signal located within a protruding peptide between the third and fourth WD domains. The amino-terminal region shows similarity to that of the Notchless WD repeat protein. Sequence comparisons revealed WDR12 orthologs in various eukaryotic species. Wdr12 seems to correspond to a single-copy gene in the mouse genome, located within the C1-C2 bands of chromosome 1. These data, together with the results of Wdr12 gene expression studies and evidence of in vitro binding of WDR12 to the cytoplasmic domain of Notch1, led us to postulate a function for the WDR12 protein in the modulation of Notch signaling activity.