AI Article Synopsis

  • Most fish typically excrete nitrogenous waste as ammonia via Rhesus glycoprotein ammonium transporters in their gills, but Alcolapia fish can adapt to alkaline soda lakes by excreting urea instead.
  • Alcolapia species retain Rhesus glycoprotein genes and can still move ammonia, but variations exist; Alcolapia grahami remains strictly ureotelic while Alcolapia alcalica also excretes ammonia.
  • Gene expression studies reveal that A. alcalica has higher levels of ammonia-related transport genes in its gills compared to A. grahami, indicating a rapid evolutionary change in the latter species toward exclusive urea excretion.

Article Abstract

Most fish excrete their nitrogenous waste across the gills as ammonia through the activity of the Rhesus glycoprotein ammonium transporters. In contrast, fish of the subgenus Alcolapia (Oreochromis) are the only vertebrates that survive the extreme conditions of the soda lakes of Natron and Magadi in East Africa and have evolved adaptations to the highly alkaline waters including the ability to excrete their nitrogenous waste as urea. Nevertheless, Alcolapia retain the Rhesus glycoprotein genes in their genomes and using two heterologous expression systems, we demonstrate that Alcolapia Rhbg is capable of moving ammonia. Comparing ammonia and urea excretion from two closely related Alcolapia species from the same aquarium, we found that while Alcolapia grahami remains fully ureotelic after many generations in lab conditions, Alcolapia alcalica excretes some of its nitrogenous waste as ammonia. Using in situ hybridisation, we demonstrate robust, localised gene expression of Rhbg, rhcg1 and rhcg2 in the gill tissue in both A. alcalica embryos and adults, similar to that in other ammoniotelic fish. In contrast, the expression of these genes in A. grahami gills is much lower than in A. alcalica, suggesting the rapid evolution of a molecular mechanism underlying the complete ureotelism of A. grahami.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672858PMC
http://dx.doi.org/10.1242/bio.059575DOI Listing

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