The fifth neurohypophysial hormone receptor is structurally related to the V2-type receptor but functionally similar to V1-type receptors

General and Comparative Endocrinology

Volumn 178, Issue 3, 2012, Pages 519-528

  Yamaguchi, Yoko ^a   Kaiya, Hiroyuki ^b   Konno, Norifumi ^c   Iwata, Eri ^d   Miyazato, Mikiya ^b   Uchiyama, Minoru ^c   Bell, Justin D ^e   Toop, Tes ^e   Donald, John A ^e   Brenner, Sydney ^f   Venkatesh, Byrappa ^f   Hyodo, Susumu ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

^c UNIVERSITY OF TOYAMA   (Japan)

^d IWAKI MEISEI UNIVERSITY   (Japan)

^e DEAKIN UNIVERSITY   (Australia)

^f INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

Author keywords

Cartilaginous fish; G protein coupled receptor; Molecular evolution; Neurohypophysial hormone; Vasotocin

Indexed keywords

ARGIPRESTOCIN; CALCIUM ION; CYCLIC AMP; NEUROHYPOPHYSIS HORMONE; OXYTOCIN; OXYTOCIN RECEPTOR; UNCLASSIFIED DRUG; VASOPRESSIN; VASOPRESSIN V1A RECEPTOR; VASOPRESSIN V1B RECEPTOR; VASOPRESSIN V2 RECEPTOR; VASOPRESSIN V2A RECEPTOR; VASOPRESSIN V2B RECEPTOR;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CALCIUM SIGNALING; EVOLUTION; HOLOCEPHALI; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PHYLOGENY; PRIORITY JOURNAL; PROTEIN FAMILY; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SYNTENY; TETRAPOD; TISSUE DISTRIBUTION; VERTEBRATE;

EID: 84864828802     PISSN: 00166480     EISSN: 10956840     Source Type: Journal    
DOI: 10.1016/j.ygcen.2012.07.008     Document Type: Article

References (36)

1. Acher R. Molecular evolution of fish neurohypophysial hormones: neutral and selective evolutionary mechanisms. Gen. Comp. Endocrinol. 1996, 102:157-172.
2. Aoyagi T., Koshimizu T.A., Tanoue A. Vasopressin regulation of blood pressure and volume: findings from V1a receptor-deficient mice. Kidney Int. 2009, 76:1035-1039.
3. Birnbaumer M. Vasopressin receptors. Trends Endocrinol. Metab. 2000, 11:406-410.
4. Donaldson Z.R., Young L.J. Oxytocin, vasopressin, and the neurogenetics of sociality. Science 2008, 322:900-904.
5. Felsenstein J. PHYLIP (Phylogeny Inference Package), Version 3.6, Distributed by the Author 2005, Department of Genome Sciences, University of Washington, Seattle.
6. Gimpl G., Fahrenholz F. The oxytocin receptor system: structure, function, and regulation. Physiol. Rev. 2001, 81:629-683.
7. Goodson J.L., Bass A.H. Forebrain peptides modulate sexually polymorphic vocal circuitry. Nature 2000, 403:769-772.
8. Guillette L.J., Norris D.O., Norman M.F. Response of amphibian (Ambystoma tigrinum) oviduct to arginine vasotocin and acetylcholine in vitro: influence of steroid hormone pretreatment in vivo. Comp. Biochem. Physiol. C: Comp. Pharmacol. Toxicol. 1985, 80:151-154.
9. Gwee P.C., Tay B.H., Brenner S., Venkatesh B. Characterization of the neurohypophysial hormone gene loci in elephant shark and the Japanese lamprey: origin of the vertebrate neurohypophysial hormone genes. BMC Evol. Biol. 2009, 9:47.
10. Hasunuma I., Sakai T., Nakada T., Toyoda F., Namiki H., Kikuyama S. Molecular cloning of three types of arginine vasotocin receptor in the newt, Cynops pyrrhogaster. Gen. Comp. Endocrinol. 2007, 151:252-258.
11. Hyodo S., Bell J.D., Healy J.M., Kaneko T., Hasegawa S., Takei Y., Donald J.A., Toop T. Osmoregulation in elephant fish Callorhinchus milii (Holocephali), with special reference to the rectal gland. J. Exp. Biol. 2007, 210:1303-1310.
12. Hyodo S., Tsukada T., Takei Y. Neurohypophysial hormones of dogfish, Triakis scyllium: structures and salinity-dependent secretion. Gen. Comp. Endocrinol. 2004, 138:97-104.
13. Kakumura K., Watanabe S., Bell J.D., Donald J.A., Toop T., Kaneko T., Hyodo S. Multiple urea transporter proteins in the kidney of holocephalan elephant fish (Callorhinchus milii). Comp. Biochem. Physiol. B: Biochem. Mol. Biol. 2009, 154:239-247.
14. Kanda A., Satake H., Kawada T., Minakata H. Novel evolutionary lineages of the invertebrate oxytocin/vasopressin superfamily peptides and their receptors in the common octopus (Octopus vulgaris). Biochem. J. 2005, 387:85-91.
15. Kawada T., Kanda A., Minakata H., Matsushima O., Satake H. Identification of a novel receptor for an invertebrate oxytocin/vasopressin superfamily peptide: molecular and functional evolution of the oxytocin/vasopressin superfamily. Biochem. J. 2004, 382:231-237.
16. Kawada T., Sekiguchi T., Itoh Y., Ogasawara M., Satake H. Characterization of a novel vasopressin/oxytocin superfamily peptide and its receptor from an ascidian, Ciona intestinalis. Peptides 2008, 29:1672-1678.
17. Kime N.M., Whitney T.K., Ryan M.J., Rand A.S., Marler C.A. Treatment with arginine vasotocin alters mating calls and decreases call attractiveness in male túngara frogs. Gen. Comp. Endocrinol. 2010, 165:221-228.
18. Kohno S., Kamishima Y., Iguchi T. Molecular cloning of an anuran V(2) type [Arg(8)] vasotocin receptor and mesotocin receptor: functional characterization and tissue expression in the Japanese tree frog (Hyla japonica). Gen. Comp. Endocrinol. 2003, 132:485-498.
19. Konno N., Hyodo S., Yamaguchi Y., Kaiya H., Miyazato M., Matsuda K., Uchiyama M. African lungfish, Protopterus annectens, possess an arginine vasotocin receptor homologous to the tetrapod V2-type receptor. J. Exp. Biol. 2009, 212:2183-2193.
20. Konno N., Kurosawa M., Kaiya H., Miyazato M., Matsuda K., Uchiyama M. Molecular cloning and characterization of V2-type receptor in two ray-finned fish, gray bichir, Polypterus senegalus and medaka, Oryzias latipes. Peptides 2010, 31:1273-1279.
21. Larkin M.A., Blackshields G., Brown N.P., Chenna R., McGettigan P.A., McWilliam H., Valentin F., Wallace I.M., Wilm A., Lopez R., Thompson J.D., Gibson T.J., Higgins D.G. Clustal W and Clustal X version 2.0. Bioinformatics 2007, 23:2947-2948.
22. Lema S.C. Identification of multiple vasotocin receptor cDNAs in teleost fish: sequences, phylogenetic analysis, sites of expression, and regulation in the hypothalamus and gill in response to hyperosmotic challenge. Mol. Cell. Endocrinol. 2010, 321:215-230.
23. Levoye A., Mouillac B., Rivière G., Vieau D., Salzet M., Breton C. Cloning, expression and pharmacological characterization of a vasopressin-related receptor in an annelid, the leech Theromyzon tessulatum. J. Endocrinol. 2005, 184:277-289.
24. Minakata H. Oxytocin/vasopressin and gonadotropin-releasing hormone from cephalopods to vertebrates. Ann. N. Y. Acad. Sci. 2010, 1200:33-42.
25. Ocampo Daza D., Lewicka M., Larhammar D. The oxytocin/vasopressin receptor family has at least five members in the gnathostome lineage, including two distinct V2 subtypes. Gen. Comp. Endocrinol. 2012, 175:135-143.
26. Oumi T., Ukena K., Matsushima O., Ikeda T., Fujita T., Minakata H., Nomoto K. Annetocin: an oxytocin-related peptide isolated from the earthworm, Eisenia foetida. Biochem. Biophys. Res. Commun. 1994, 198:393-399.
27. Pierce J.G., du Vigneaud V. Studies on high potency oxytocic material from beef posterior pituitary lobes. J. Biol. Chem. 1950, 186:77-84.
28. Rodríguez M., Specker J.L. In vitro effects of arginine vasotocin on testosterone production by testes of rainbow trout (Oncorhynchus mykiss). Gen. Comp. Endocrinol. 1991, 83:249-257.
29. Ronquist F., Teslenko M., van der Mark P., Ayres D.L., Darling A., Höhna S., Larget B., Liu L., Suchard M.A., Huelsenbeck J.P. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst. Biol. 2012, 10.1093/sysbio/sys029.
30. Stafflinger E., Hansen K.K., Hauser F., Schneider M., Cazzamali G., Williamson M., Grimmelikhuijzen C.J. Cloning and identification of an oxytocin/vasopressin-like receptor and its ligand from insects. Proc. Natl. Acad. Sci. USA 2008, 105:3262-3267.
31. Suzuki M., Kubokawa K., Nagasawa H., Urano A. Sequence analysis of vasotocin cDNAs of the lamprey, Lampetra japonica, and the hagfish, Eptatretus burgeri: evolution of cyclostome vasotocin precursors. J. Mol. Endocrinol. 1995, 14:67-77.
32. Tan F.L., Lolait S.J., Brownstein M.J., Saito N., MacLeod V., Baeyens D.A., Mayeux P.R., Jones S.M., Cornett L.E. Molecular cloning and functional characterization of a vasotocin receptor subtype that is expressed in the shell gland and brain of the domestic chicken. Biol. Reprod. 2000, 62:8-15.
33. Turner R.A., Pierce J.G., du Vigneaud V. The purification and the amino acid content of vasopressin preparations. J. Biol. Chem. 1951, 191:21-28.
34. Urano A., Hyodo S., Suzuki M. Molecular evolution of neurohypophysial hormone precursors. Prog. Brain Res. 1992, 92:39-46.
35. van Kesteren R.E., Tensen C.P., Smit A.B., van Minnen J., van Soest P.F., Kits K.S., Meyerhof W., Richter D., van Heerikhuizen H., Vreugdenhil E., Geraerts W.P.M. A novel G protein-coupled receptor mediating both vasopressin- and oxytocin-like functions of Lys-conopressin in Lymnaea stagnalis. Neuron 1995, 15:897-908.
36. Venkatesh B., Kirkness E.F., Loh Y.H., Halpern A.L., Lee A.P., Johnson J., Dandona N., Viswanathan L.D., Tay A., Venter J.C., Strausberg R.L., Brenner S. Survey sequencing and comparative analysis of the elephant shark (Callorhinchus milii) genome. PLoS Biol. 2007, 5:e101.