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I conducted an 18 month study on the behavior and ecology of two species of sympatric caviid rodents (Kerodon rupestris and Galea spixii) in northeastern Brazil. Preliminary observations indicated that Kerodon was a habitat specialist. occurring only in large boulder piles. whereas Galea appeared to be a habitat generalist. occurring in a variety of open habitats excepting the boulder piles inhabited by Kerodon. This situation presented an ideal field experiment to compare the social structures in these two closely related genera. I first established breeding colonies of both in order to describe their behavioral displays and to discern their function. Complete behavioral repeltoires. including vocalizations. are presented for both Kerodon and Galea. Reproduction and growth. behavioral development. sexual behavior. agonistic behavior. and use of space were all examined both quantitatively and qualitatively in the colonies and in the field. Time budgets were calculated and analyzed for both genera. Differences in rates of growth and behavioral development between the two genera afe probably related to ecological aspects of their significantly different microhabitat preferences. Data on sexual and agonistic behavior collected in the colonies suggested that Kerodon exhibited resource defense polygyny, whereas the Galea mating system approximated male dominance polygyny. Field data supported the colony observations. These differences in mating systems may be related to the different habitat preferences observed. Kerodvll is compared to other resource defense polygynists. Finally, a model for the evolution of behavior in the family Caviidae is presented. The social organizations of the various genera seem to be very responsive to ecological requirements. The importance of social organization in ecological adaptation is discussed.
Previous studies in developing Xenopus and zebrafish reported that the phosphate transporter slc20a1a is expressed in pronephric kidneys. The recent identification of SLC20A1 as a monoallelic candidate gene for cloacal exstrophy further suggests its involvement in the urinary tract and urorectal development. However, little is known of the functional role of SLC20A1 in urinary tract development. Here, we investigated this using morpholino oligonucleotide knockdown of the zebrafish ortholog slc20a1a. This caused kidney cysts and malformations of the cloaca. Moreover, in morphants we demonstrated dysfunctional voiding and hindgut opening defects mimicking imperforate anus in human cloacal exstrophy. Furthermore, we performed immunohistochemistry of an unaffected 6-week-old human embryo and detected SLC20A1 in the urinary tract and the abdominal midline, structures implicated in the pathogenesis of cloacal exstrophy. Additionally, we resequenced SLC20A1 in 690 individuals with bladder exstrophy-epispadias complex (BEEC) including 84 individuals with cloacal exstrophy. We identified two additional monoallelic de novo variants. One was identified in a case-parent trio with classic bladder exstrophy, and one additional novel de novo variant was detected in an affected mother who transmitted this variant to her affected son. To study the potential cellular impact of SLC20A1 variants, we expressed them in HEK293 cells. Here, phosphate transport was not compromised, suggesting that it is not a disease mechanism. However, there was a tendency for lower levels of cleaved caspase-3, perhaps implicating apoptosis pathways in the disease. Our results suggest SLC20A1 is involved in urinary tract and urorectal development and implicate SLC20A1 as a disease-gene for BEEC.