Aquaporin molecular characterization in the sea-bass (Dicentrarchus labrax): The effect of salinity on AQP1 and AQP3 expression

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 148, Issue 2, 2007, Pages 430-444

  Giffard Mena, Ivone ^a   Boulo, Viviane ^a   Aujoulat, Fabien ^a   Fowden, Holly ^b   Castille, René ^a   Charmantier, Guy ^a   Cramb, Gordon ^b  

^a UNIVERSITÉ MONTPELLIER 2   (France)

^b UNIVERSITY OF ST ANDREWS   (United Kingdom)

Author keywords

Aquaporins; Gill; Intestine; Kidney; Osmoregulation; Salinity adaptation; Teleost fish; Water channel

Indexed keywords

AQUAPORIN; AQUAPORIN 1; AQUAPORIN 3; COMPLEMENTARY DNA; WATER;

AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DIGESTIVE SYSTEM; DNA SEQUENCE; ENVIRONMENTAL EXPOSURE; EUROPEAN SEA BASS; GILL; ION EXCHANGE; KIDNEY; NONHUMAN; NUCLEOTIDE SEQUENCE; OSMOREGULATION; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN ISOLATION; SALINITY; WATER TRANSPORT;

DICENTRARCHUS LABRAX; MAMMALIA; SERRANIDAE; TELEOSTEI;

EID: 34547572757     PISSN: 10956433     EISSN: 15314332     Source Type: Journal    
DOI: 10.1016/j.cbpa.2007.06.002     Document Type: Article

References (56)

1. Agre P., Borgnia M., Yasui M., Neely J.D., Carbrey J., Kozono D., Beitz E., Hoffert J., Leitch V., and King S.L. Discovery of the aquaporins and their impact on basic and clinical physiology. In: Hohmann S., Nielsen S., and Agre P. (Eds). Aquaporins. Current topics in Membranes vol. 51 (2001), Academic Press, San Diego, California, USA 1-37
2. Altschul S., Madden T., Schaffer A., Zhang J., Zhang Z., Miller W., and Lipman D. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25 (1997) 3389-3402
3. Ando M., Mukuda T., and Kozaka T. Water metabolism in the eel acclimated to sea water: from mouth to intestine. Comp. Biochem. Physiol. A 136 (2003) 621-633
4. Aoki M., Kaneko T., Katoh F., Hasegawa S., Tsutsui N., and Aida K. Intestinal water absorption through aquaporin 1 expressed in the apical membrane of mucosal epithelial cells in seawater-adapted Japanese eel. J. Exp. Biol. 206 (2003) 3495-3505
5. Beyst B., Hostens K., and Mees J. Factors influencing fish and macrocrustacean communities in the surf zone of sandy beaches in Belgium: temporal variation. J. Sea Res. 46 (2001) 281-294
6. Borgnia M., Nielsen S., Engel A., and Agre P. Cellular and molecular biology of the aquaporin water channels. Annu. Rev. Biochem. Allied Res. India 68 (1999) 425-458
7. Buck T.M., Eledge J., and Skach W.R. Evidence for stabilization of aquaporin-2 folding mutants by N-linked glycosylation in endoplasmic reticulum. Am. J. Physiol., Cell. Physiol. 287 (2004) C1292-C1299
8. Chomczynski P., and Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162 (1987) 156-159
9. Cutler C., and Cramb G. Water transport and aquaporin expression in fish. In: Hohmann S., Nielsen S., and Agre P. (Eds). Molecular Biology and Physiology of Water and Solute Transport (2000), Kluwer academic press, London, UK 431-441
10. Cutler C.P., Brezillon S., Bekir S., Sanders I.L., Hazon N., and Cramb G. Expression of a duplicate Na, K-ATPase beta 1-isoform in the European eel (Anguilla anguilla). Am. J. Physiol., Regul. Integr. Comp. Physiol. 279 (2000) R222-R229
11. Cutler C.P., and Cramb G. Molecular physiology of osmoregulation in eels and other teleosts: the role of transporter isoforms and gene duplication. Comp. Biochem. Physiol. A 130 (2001) 551-564
12. Cutler C.P., and Cramb G. Branchial expression of an aquaporin 3 (AQP-3) homologue is downregulated in the European eel Anguilla anguilla following seawater acclimation. J. Exp. Biol. 205 (2002) 2643-2651
13. C.P. Cutler, A.S. Martinez, G. Cramb, (in press). The role of aquaporin 3 in teleost fish. Comp. Biochem. Physiol. A.
14. +-ATPase β1 subunit in the European eel (Anguilla anguilla). Fish Physiol. Biochem. 14 (1995) 423-429
15. Evans D.H. Osmotic and ionic regulation. In: Evans D.H. (Ed). The Physiology of Fishes (1993), CRC Press, Boca Raton, Fla. 315-341
16. Fabra M., Raldua D., Power D.M., Deen P.M.T., and Cerda J. Marine fish egg hydration is aquaporin-mediated. Science 307 (2005) 545
17. Giffard-Mena I., Charmantier G., Grousset E., Aujoulat F., and Castille R. Digestive tract ontogeny of Dicentrarchus labrax: implication in osmoregulation. Dev. Growth Differ. 48 (2006) 139-151
18. Gouret P., Vitiello V., Balandraud N., Gilles A., Pontarotti P., and Danchin E. FIGENIX: intelligent automation of genomic annotation: expertise integration in a new software platform. BMC Bioinformatics 6 (2005) 198
19. Hall T. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 41 (1999) 95-98
20. Hampel H., Cattrijsse A., and Mees J. Changes in marsh nekton communities along the salinity gradient of the Schelde river, Belgium and The Netherlands. Hydrobiologia 515 (2004) 137-146
21. Haywood G.P., Isaia J., and Maetz J. Epinephrine effects on branchial water and urea flux in rainbow trout. Am. J. Physiol., Regul. Integr. Comp. Physiol. 232 (1977) R110-R115
22. Hohmann S., Nielsen S., and Agre P. Aquaporins. Current Topics in Membranes (2001), Academic Press, San Diego, California, USA
23. Hulo N., Sigrist C.J.A., Le Saux V., Langendijk-Genevaux P.S., Bordoli L., Gattiker A., De Castro E., Bucher P., and Bairoch A. Recent improvements to the PROSITE database. Nucleic Acids Res. 32 (2004) 134-137
24. Isaia J. Water and nonelectolyte permeation. In: Hoar W.S., and Randall D.J. (Eds). Fish Physiology, vol. X, Gills; Part B, Ion and Water Transfer (1984), Academic Press, New York 1-38
25. Ishibashi K. Aquaporin subfamily with unusual NPA boxes. Biochim. Biophys. Acta 1758 (2006) 989-993
26. Jennings S., and Pawson M.G. The origin and recruitment of bass, Dicentrarchus labrax, larvae to nursery areas. J. Mar. Biol. Assoc. UK 72 (1992) 199-212
27. +-ATPase in the gills of European sea bass, Dicentrarchus labrax (L.). J. Exp. Zool. 282 (1998) 290-300
28. Karnaky K.J.J. Osmotic and ionic regulations. In: Evans D.H. (Ed). The physiology of Fishes (1998), CRC Press, Boca Raton 157-176
29. Katoh K., Kuma K., Toh H., and Miyata T. MAFFT version 5: improvement in accuracy of multiple sequence alignment. Nucl. Acids Res. 33 (2005) 511-518
30. Kelley D.F. The importance of estuaries for sea-bass, Dicentrarchus labrax (L.). J. Fish Biol. 33 (1988) 25-33
31. Kyte J., and Doolittle R.F. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157 (1982) 105-132
32. +)-dependent ATPase activity in gills and kidneys of two euryhaline marine teleosts, Crenimugil labrosus (Risso, 1826) and Dicentrarchus labrax (Linnaeus, 1758), during adaptation to fresh water. Life Sci. 10 (1971) 113-119
33. Lignot J.H., Cutler C.P., Hazon N., and Cramb G. Immunolocalisation of aquaporin 3 in the gill and the gastrointestinal tract of the European eel Anguilla anguilla (L.). J. Exp. Biol. 205 (2002) 2653-2663
34. Ma T., and Verkman A.S. Aquaporin water channels in gastrointestinal physiology. J. Physiol. (Lond.) 517 (1999) 317-326
35. Martinez A.S., Cutler C.P., Wilson G.D., Philips C., Hazon N., and Cramb G. Cloning and expression of three aquaporin homologues from the European eel (Anguilla anguilla): effects of sea water acclimation and cortisol treatment on renal expression. Biol. Cell 97 (2005) 615-627
36. Martinez A.S., Cutler C.P., Wilson G.D., Phillips C., Hazon N., and Cramb G. Regulation of expression of two aquaporin homologs in the intestine of the European eel: effects of seawater acclimation and cortisol treatment. Am. J. Physiol. Regul. Integr. Comp. Physiol. 288 (2005) R1733-R1743
37. Matsuzaki T., Suzuki T., and Takata K. Water channel protein aquaporin 3, in epithelial cells. In: Hohmann S., and Nielsen S. (Eds). Molecular Biology and Physiology of Water and Solute Transport (2000), Kluwer Academic/Plenum Publishers, New York 167-171
38. Motais R., and Isaia J. Temperature-dependence of permeability to water and to sodium of the gill epithelium of the Eel Anguilla anguilla. J. Exp. Biol. 56 (1972) 587-600
39. Motais R., Isaia J., Rankin J.C., and Maetz J. Adaptive changes of the water permeability of the teleostean gill epithelium in relation to external salinity. J. Exp. Biol. 51 (1969) 529-546
40. Moustakas C.T., Watanabe W.O., and Copeland K.A. Combined effects of photoperiod and salinity on growth, survival, and osmoregulatory ability of larval southern flounder Paralichthys lethostigma. Aquaculture 229 (2004) 159-179
41. Nebel C., Nègre-Sadargues G., Blasco C., and Charmantier G. Morpho-functional ontogeny of the urinary system of the European sea bass Dicentrarchus labrax. Anat. Embryol. 209 (2005) 193-206
42. Nebel C., Romestand B., Negre-Sadargues G., Grousset E., Aujoulat F., Bacal J., Bonhomme F., and Charmantier G. Differential freshwater adaptation in juvenile sea-bass Dicentrarchus labrax: involvement of gills and urinary system. J. Exp. Biol. 208 (2005) 3859-3871
43. Nielsen S., Kwon T.H., Frokiaer J., and Agre P. Regulation and dysregulation of aquaporins in water balance disorders. J. Intern. Med. 261 (2007) 53-64
44. Picket G.D., and Pawson M.G. Sea bass: biology, exploitation and conservation. In: Pitcher T.J. (Ed). Fish and Fisheries Series vol. 12 (1994), Chapman and Hall, London 1-235
45. Preston G., and Agre P. Isolation of the cDNA for erythrocyte integral membrane protein of 28 kDa : member of an ancient channel family. Proc. Natl. Acad. Sci. U. S. A. 88 (1991) 11110-11114
46. Preston G.M., Carroll T.P., Guggino W.B., and Agre P. Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein. Science 256 (1992) 385-387
47. Santos C.R.A., Estevao M.D., Fuentes J., Cardoso J.C.R., Fabra M., Passos A.L., Detmers F.J., Deen P.M.T., Cerda J., and Power D.M. Isolation of a novel aquaglyceroporin from a marine teleost (Sparus auratus): function and tissue distribution. J. Exp. Biol. 207 (2004) 1217-1227
48. Sayer M.D.J., and Davenport J. The relative importance of the gills to ammonia and urea excretion in five seawater and one freshwater teleost species. J. Fish Biol. 31 (1987) 561-570
49. Schrier R.W., Chen Y.C., and Cadnapaphornchai M.A. From finch to fish to man: Role of aquaporins in body fluid and brain water regulation. Neuroscience 129 (2004) 897-904
50. Stahlberg H., Heymann B., Mitsouoka K., Fuyijoshi Y., and Engel A. The Aquaporin Superfamily. In: Hohmann S., N.S. P., and Agre (Eds). Aquaporins. Current topics in Membranes vol. 51 (2001), Academic Press, San Diego, California, USA 39-119
51. Varsamos S., Diaz J.P., Charmantier G., Blasco C., Connes R., and Flik G. Location and morphology of chloride cells during the postembryonic development of the European sea bass, Dicentrarchus labrax. Anat. Embryol. 205 (2002) 203-213
52. Varsamos S., Diaz J.P., Charmantier G., Flik G., Blasco C., and Connes R. Branchial chloride cells in sea bass (Dicentrarchus labrax) adapted to fresh water, seawater, and doubly concentrated seawater. J. Exp. Zool. 293 (2002) 12-26
53. Varsamos S., Nebel C., and Charmantier G. Ontogeny of osmoregulation in postembryonic fish: A review. Comp. Biochem. Physiol. A 141 (2005) 401-429
54. Verkman A.S., and Mitra A.K. Structure and function of aquaporin water channels. Am. J. Physiol., Renal. Physiol. 278 (2000) F13-F28
55. Wang D.Y.C., Kumar S., and Hedges S.B. Divergence time estimates for the early history of animal phyla and the origin of plants, animals and fungi. Proc. R. Soc. Lond., B 266 (1999) 163
56. Watanabe S., Kaneko T., and Aida K. Aquaporin-3 expressed in the basolateral membrane of gill chloride cells in Mozambique tilapia Oreochromis mossambicus adapted to freshwater and seawater. J. Exp. Biol. 208 (2005) 2673-2682