The zebrafish cationic amino acid transporter/glycoprotein-associated family: sequence and spatiotemporal distribution during development of the transport system b0,+ (slc3a1/slc7a9)

• Published in: Fish physiology and biochemistry Vol. 47; no. 5; pp. 1507 - 1525
• Main Authors: Ellingsen, Ståle, Narawane, Shailesh, Fjose, Anders, Verri, Tiziano, Rønnestad, Ivar
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.10.2021; Springer Nature B.V
• Subjects: absorption; Amino acid sequence; amino acid transporters; Amino acids; Animal Anatomy; Animal Biochemistry; Animal Physiology; Arginine; Biological fertilization; Biomedical and Life Sciences; Cations; Conserved sequence; Cystine; Cystinuria; Danio rerio; Epithelial cells; Epithelium; Evolutionary conservation; Fertilization; Fish; Freshwater & Marine Ecology; Freshwater fishes; Gene expression; Genes; Genomes; germplasm conservation; Glycoproteins; Histology; Hybridization; Intestine; Intestines; Kidneys; Life Sciences; Lysine; Mammals; Morphology; Mutation; Nutrients; Ornithine; Phylogeny; Sequence analysis; Sequencing; Spatial distribution; Substrates; Synteny; Temporal distribution; Transport; Transportation systems; Zebrafish; Zoology; Proximal convoluted tubule; Proximal straight tubule; Heteromeric amino acid transporters; Kidney; Gut
• ISSN: 0920-1742; 1573-5168; 1573-5168
• DOI: 10.1007/s10695-021-00984-z

System b 0,+ absorbs lysine, arginine, ornithine, and cystine, as well as some (large) neutral amino acids in the mammalian kidney and intestine. It is a heteromeric amino acid transporter made of the heavy subunit SLC3A1/rBAT and the light subunit SLC7A9/b 0,+ AT. Mutations in these two genes can cause cystinuria in mammals. To extend information on this transport system to teleost fish, we focused on the slc3a1 and slc7a9 genes by performing comparative and phylogenetic sequence analysis, investigating gene conservation during evolution (synteny), and defining early expression patterns during zebrafish ( Danio rerio ) development. Notably, we found that slc3a1 and slc7a9 are non-duplicated in the zebrafish genome. Whole-mount in situ hybridization detected co-localized expression of slc3a1 and slc7a9 in pronephric ducts at 24 h post-fertilization and in the proximal convoluted tubule at 3 days post-fertilization (dpf). Notably, both the genes showed co-localized expression in epithelial cells in the gut primordium at 3 dpf and in the intestine at 5 dpf (onset of exogenous feeding). Taken together, these results highlight the value of slc3a1 and slc7a9 as markers of zebrafish kidney and intestine development and show promise for establishing new zebrafish tools that can aid in the rapid screening(s) of substrates. Importantly, such studies will help clarify the complex interplay between the absorption of dibasic amino acids, cystine, and (large) neutral amino acids and the effect(s) of such nutrients on organismal growth.