Distribution of vasotocin- and mesotocin-like immunoreactivities in the brain of the South African clawed frog Xenopus-laevis

1992 ◽  
Vol 5 (6) ◽  
pp. 465-479 ◽  
Author(s):  
Agustin González ◽  
Wilhelmus J.A.J. Smeets
1995 ◽  
Vol 9 (1) ◽  
pp. 27-40 ◽  
Author(s):  
A. González ◽  
A. Mun˜oz ◽  
M. Mun˜oz ◽  
O. Marín ◽  
W.J.A.J. Smeets

Endocrinology ◽  
2005 ◽  
Vol 146 (11) ◽  
pp. 4851-4860 ◽  
Author(s):  
Graham C. Boorse ◽  
Erica J. Crespi ◽  
Frank M. Dautzenberg ◽  
Robert J. Denver

Several corticotropin-releasing factor (CRF) family genes have been identified in vertebrates. Mammals have four paralogous genes that encode CRF or the urocortins 1, 2, and 3. In teleost fishes, a CRF, urotensin I (a fish ortholog of mammalian urocortin 1) and urocortin 3 have been identified, suggesting that at least three of the four mammalian lineages arose in a common ancestor of modern bony fishes and tetrapods. Here we report the isolation of genes orthologous to mammalian urocortin 1 and urocortin 3 from the South African clawed frog, Xenopus laevis. We characterize the pharmacology of the frog peptides and show that X. laevis urocortin 1 binds to and activates the frog CRF1 and CRF2 receptors at picomolar concentrations. Similar to mammals, frog urocortin 3 is selective for the CRF2 receptor. Only frog urocortin 1 binds to the CRF-binding protein, although with significantly lower affinity than frog CRF. Both urocortin genes are expressed in brain, pituitary, heart, and kidney of juvenile frogs; urocortin 1 is also expressed in skin. We also identified novel urocortin sequences in the genomes of pufferfish, zebrafish, chicken, and dog. Phylogenetic analysis supports the view that four paralogous lineages of CRF-like peptides arose before the divergence of the actinopterygian and sarcopterygian fishes. Our findings show that the functional relationships among CRF ligands and binding proteins, and their anorexigenic actions mediated by the CRF2 receptor, arose early in vertebrate evolution.


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