Regulation of hepatic estrogen receptor isoform mRNA expression in rainbow trout (Oncorhynchus mykiss)

General and Comparative Endocrinology

Volumn 161, Issue 1, 2009, Pages 73-78

  Boyce Derricott, Josh ^a   Nagler, James J ^a   Cloud, J G ^a  

^a UNIVERSITY OF IDAHO   (United States)

Author keywords

Estrogen receptor; Ethynylestradiol; Isoform; Isogenic; Trout

Indexed keywords

ESTRADIOL; ESTROGEN RECEPTOR; ESTROGEN RECEPTOR ALPHA; ESTROGEN RECEPTOR ALPHA1; ESTROGEN RECEPTOR ALPHA2; ESTROGEN RECEPTOR BETA; ESTROGEN RECEPTOR BETA2; ETHINYLESTRADIOL; ISOPROTEIN; MESSENGER RNA; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENZYME REGULATION; IN VIVO STUDY; MALE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAINBOW TROUT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

EID: 60549092676     PISSN: 00166480     EISSN: 10956840     Source Type: Journal    
DOI: 10.1016/j.ygcen.2008.11.022     Document Type: Article

References (53)

1. Amores A., Force A., Yan Y.-L., Joly L., Amemiya C., Fritz A., Ho R.K., Langeland J., Prince V., Wang Y.-L., Westerfield M., Ekker M., and Postlethwait J.H. Zebrafish hox clusters and vertebrate genome evolution. Science 282 (1998) 1711-1714
2. Babich H., and Borenfreund E. Cytotoxicity and genotoxicity assays with cultured fish cells: A review. Toxicol. In Vitro 5 (1991) 91-100
3. Bennetau-Pelissero C., Fluoriot G., Valotaire Y., Sumpter J.P., and Le Menn F. Induction of rainbow trout estradiol receptor mRNA and vitellogenin mRNA by phytoestrogens in hepatocyte cultures. Ann. NY Acad. Sci. 839 (1998) 600-601
4. Bennetau-Pelissero C., Breton B.B., Bennetau B., Corraze G., Le Menn F., Davail-Cuisset B., Helou C., and Kaushik S.J. Effect of genistein-enriched diets on the endocrine process of gametogenesis and on reproduction efficiency of the rainbow trout Oncorhynchus mykiss. Gen. Comp. Endocrinol. 121 (2001) 173-187
5. Bortone S.A., and Davis W.P. Fish intersexuality as indicator of environmental stress. BioScience 44 (1994) 165-172
6. Brown K.H., Schultz I.R., and Nagler J.J. Reduced embryonic survival in rainbow trout resulting from paternal exposure to the environmental estrogen 17α-ethynylestradiol during late sexual maturation. Reproduction 134 (2007) 659-666
7. Cao Z., Hong J., Peterson R.E., and Aiken J.M. Characterization of CYP1A and CYP1A3 gene expression in rainbow trout (Oncorhynchus mykiss). Aquat. Toxicol. 49 (2000) 101-109
8. Choi C.Y., and Habibi H.R. Molecular cloning of estrogen receptor α and expression pattern of estrogen receptor subtypes in male and female goldfish. Mol. Cell Endocrinol. 204 (2003) 169-177
9. Christianson-Heiska I., and Isomaa B. The use of primary hepatocytes from brown trout (Salmo trutta lacustris) and the fish cell lines RTH-149 and ZF-L for in vitro screening of (anti)estrogenic activity of wood extractives. Toxicol. In Vitro 22 (2008) 589-597
10. Edwards D.P. Regulation of signal transduction pathways by estrogen and progesterone. Ann. Rev. Physiol. 67 (2005) 335-376
11. Evans R.M. The steroid and thyroid hormone receptor superfamily. Science 240 (1988) 889-895
12. Fent K. Fish cell lines as versatile tools in ecotoxicology: assessment of cytotoxicity, cytochrome P4501A induction potential and estrogenic activity of chemicals and environmental samples. Toxicol. In Vitro 15 (2001) 477-488
13. Filby A.L., and Tyler C.R. Molecular characterization of estrogen receptors 1, 2a, and 2b and their tissue and ontogenic expression rofiles in fathead minnow (Pimephales promelas). Biol. Reprod. 73 (2005) 648-662
14. Flouriot G., Pakdel F., Ducouret B., Ledrean Y., and Valotaire Y. Differential regulation of two genes implicated in fish reproduction: vitellogenin and estrogen receptor genes. Mol. Reprod. Dev. 48 (1997) 317-323
15. Flouriot G., Pakdel F., and Valotaire Y. Transcriptional and post-transcriptional regulation of rainbow trout estrogen receptor and vitellogenin gene expression. Mol. Cell Endocrinol. 124 (1996) 173-183
16. Force A., Lynch M., Pickett B., Amores A., Yan Y.-l., and Postlethwait J. Preservation of duplicate genes by complementary, degenerative mutations. Genetics 151 (1999) 1531-1545
17. Gilsbach R., Kouta M., Bonisch H., and Bruss M. Comparison of in vitro and in vivo reference genes for internal standardization of real-time PCR data. Biotechniques 40 (2006) 173-177
18. Hawkins M.B., Thornton J.W., Crews D., Skipper J.K., Dotte A., and Thomas P. Identification of a third distinct estrogen receptor and reclassification of estrogen receptors in teleosts. Proc. Natl. Acad. Sci. USA 97 (2000) 10751-10756
19. Jobling S., Nolan M., Tyler C.R., Brighty G., and Sumpter J.P. Widespread sexual disruption in wild fish. Environ. Sci. Technol. 32 (1998) 2498-2506
20. Kamer I., and Rinkevich B. In vitro application of the comet assay for aquatic genotoxicity: considering a primary culture versus a cell line. Toxicol. In Vitro 16 (2002) 177-184
21. Kolpin D.W., Furlong E.T., Meyer M.T., Thurman E.M., Zaugg S.D., Barber L.B., and Buxton H.T. Pharmaceuticals, hormones, and other organic wastewater contaminants in US streams, 1999-2000: A national reconnaissance. Environ. Sci. Technol. 36 (2002) 1202-1211
22. Lannan C.N., Winton J.R., and Fryer J.L. Fish cell lines: establishment and characterization of nine cell lines from salmonids. In Vitro 20 (1984) 671-675
23. Leanos-Castaneda O., and Van Der Kraak G. Functional characterization of estrogen receptor subtypes, ERα and ERβ, mediating vitellogenin production in the liver of rainbow trout. Toxicol. Appl. Pharmacol. 224 (2007) 116-125
24. Le Drean Y., Pakdel F., and Valotaire Y. Structure and regulation of genes for estrogen receptors. Fish Physiol. XIII (1994) 331-366
25. MacKay M.E., Raelson J., and Lazier C.B. Up-regulation of estrogen receptor mRNA and estrogen receptor activity by estradiol in liver of rainbow trout and other teleostean fish. Comp. Biochem. Physiol. C: Pharmacol. Toxicol. Endocrinol. 115 (1996) 201-209
26. Mannerström M., Tahti H., Tiihonen K., and Salama A. d-Glucose uptake in fish hepatocytes: mediated by transporter in rainbow trout (Oncorhynchus mykiss), but only by diffusion in prespawning lamprey (Lampetra fluviatilis) and in RTH-149 cell line. Comp. Biochem. Physiol. A 136 (2003) 779-790
27. Martyniuk C.J., Gerrie E.R., Popesku J.T., Ekker M., and Trudeau V.L. Microarray analysis in the zebrafish (Danio rerio) liver and telencephalon after exposure to low concentration of 17α-ethinylestradiol. Aquat. Toxicol. 84 (2007) 38-49
28. Matsumoto T., Kobayashi M., Moriwaki T., Kawai S., and Watabe S. Survey of estrogenic activity in fish feed by yeast estrogen-screen assay. Comp. Biochem. Physiol. C 139 (2004) 147-152
29. Matthews J., and Gustafsson J.-A. Estrogen signaling: a subtle balance between ERα and ERβ. Mol. Interv. 3 (2003) 281-292
30. Menuet A., Le Page Y., Torres O., Kern L., Kah O., and Pakdel F. Analysis of the estrogen regulation of the zebrafish estrogen receptor (ER) reveals distinct effects of ERα, ERβ1 and ERβ2. J. Mol. Endocrinol. 32 (2004) 975-986
31. Menuet A., Pellegrini E., Anglade I., Blaise O., Laudet V., Kah O., and Pakdel F. Molecular characterization of three estrogen receptor forms in zebrafish: binding characteristics, transactivation properties, and tissue distributions. Biol. Reprod. 66 (2002) 1881-1892
32. Meyer A., and Van de Peer Y. From 2R to 3R: evidence for a fish-specific genome duplication (FSGD). Bioessays 27 (2005) 937-945
33. Mortensen A.S., and Arukwe A. Effects of 17α-ethynylestradiol on hormonal responses and xenobiotic biotransformation system of Atlantic salmon (Salmo salar). Aquat. Toxicol. 85 (2007) 113-123
34. Nagler J.J., Cavileer T., Sullivan J., Cyr D.G., and Rexroad III C. The complete nuclear estrogen receptor family in the rainbow trout: discovery of the novel ERα2 and both ERβ isoforms. Gene 392 (2007) 164-173
35. Nelson E.R., Wiehler W.B., Cole W.C., and Habibi H.R. Homologous regulation of estrogen receptor subtypes in goldfish (Carassius auratus). Mol. Reprod. Dev. 74 (2007) 1105-1112
36. Olsson P.-E., Hyllner S.J., Zafarullah M., Andersson T., and Gedamu L. Differences in metallothionein gene expression in primary cultures of rainbow trout hepatocytes and the RTH-149 cell line. Biochim. Biophys. Acta 1049 (1990) 78-82
37. Ostrander G.K., Blair J.B., Stark B.A., Marley G.M., Bales W.D., Veltri R.W., Hinton D.E., Okihiro M., Ortego L.S., and Hawkins W.E. Long-term primary culture of epithelial cells from rainbow trout (Oncorhynchus mykiss) liver. In Vitro Cell Dev. Biol. Anim. 31 (1995) 367-378
38. Pelissero C., Fluoriot G., Foucher J.L., Bennetau B., Dunogues J., Le Gac F., and Sumpter J.P. Vitellogenin synthesis in cultured hepatocytes; an in vitro test for the estrogenic potency of chemicals. J. Ster. Biochem. Mol. Biol. 44 (1993) 263-272
39. Perry G.M.L., McDonald G.J., Ferguson M.M., Ganassin R.C., and Bols N.C. Characterization of rainbow trout cell lines using microsatellite DNA profiling. Cytotechnology 37 (2001) 143-151
40. Roy A.K. Regulation of steroid hormone action in target cells by specific hormone-inactivating enzymes. Proc. Soc. Exp. Biol. Med. 199 (1992) 265-272
41. Sabo-Attwood T., Kroll K.J., and Denslow N.D. Differential expression of largemouth bass (Micropterus salmoides) estrogen receptor isotypes α, β, and γ by estradiol. Mol. Cell Endocrinol. 218 (2004) 107-118
42. Schultz I.R., Orner G., Merdink J.L., and Skillman A. Dose-response relationships and pharmacokinetics of vitellogenin in rainbow trout after intravascular administration of 17α-ethynylestradiol. Aquat. Toxicol. 51 (2001) 305-318
43. Schultz I.R., Skillman A., Nicolas J.-M., Cyr D.G., and Nagler J.J. Short term exposure to 17α-ethynylestradiol decreases the fertility of sexually maturing male rainbow trout, (Oncorhynchus mykiss). Environ. Toxicol. Chem. 22 (2003) 1272-1280
44. Sheahan D.A., Bucke D., Matthiessen P., Sump[ter J.P., Kirby M.F., Neall P., and Waldock M. The effects of low levels of 17α-ethynylestradiol upon plasma vitellogenin levels in male and female rainbow trout, Oncorhynchus mykiss. In: Muller R., and Lloyd R. (Eds). Sublethal and Chronic Effects of Pollutants n Freshwater fish (1994), Fishing News Books, London, UK 99-112
45. Skillman A.D., Nagler J.J., Hook S.E., Small J.A., and Schultz I.R. Dynamics of 17α-ethynylestradiol exposure in rainbow trout (Oncorhynchus mykiss): absorption, tissue distribution, and hepatic gene expression pattern. Environ. Toxicol. Chem. 25 (2006) 2997-3005
46. Soverchia L., Ruggeri B., Palermo F., Mosconi G., Cardinaletti G., Scortichini G., Gatti G., and Polzonetti-Magni A.M. Modulation of vitellogenin synthesis through estrogen receptor β-1 in goldfish (Carassius auratus) juveniles exposed to 17-β estradiol and nonylphenol. Toxicol. Appl. Pharmacol. 209 (2005) 236-243
47. Sumpter J., and Jobling S. Vitellogenesis as a biomarker for estrogenic contamination of the aquatic environment. Environ. Health. Perspect. 103 (1995) 173-178
48. Thomas-Jones E., Thorpe K., Harrison N., Thomas G., Morris C., Huchison T., Woodhead S., and Tyler C. Dynamics of estrogen biomarker responses in rainbow trout exposed to 17β-estradiol and 17α-ethinylestradiol. Environ. Toxicol. Chem. 22 (2003) 3001-3008
49. Tsuji P.A., and Walle T. Cytoxic effects of the dietary flavones chrysin and apigenin in a normal trout liver cell line. Chemico-Biol. Interact. 171 (2008) 37-44
50. Wallace R. Vitellogenesis and oocyte growth in nonmammalian vertebrates. In: Browder L.W. (Ed). Developmental Biology (1985), Plenum Press, New York 127-178
51. Williams C., Edvardsson K., Lewandowski S.A., Strom A., and Gustafsson J.A. A genome-wide study of the repressive effects of estrogen receptor β on estrogen receptor α signaling in breast cancer cells. Oncogene 27 (2007) 1019-1032
52. Zeng Q., Chen G.G., Vlantis A.C., Tse G.M., and van Hasselt C.A. The contributions of oestrogen receptor isoforms to the development of papillary and anaplastic thyroid carcinomas. J. Pathol. 214 (2008) 425-433
53. Zhang X., Hecker M., Park J.-W., Tompsett A.R., Newsted J., Nakayama K., Jones P.D., Au D., Kong R., Wu R.S.S., and Giesy J.P. Real-time PCR array to study effects of chemicals on the hypothalamic-pituitary-gonadal axis of the Japanese medaka. Aquat. Toxicol. 88 (2008) 173-182