Characterization of vtg-1 mRNA expression during ontogeny in Oreochromis mossambicus (PETERS)

Journal of Steroid Biochemistry and Molecular Biology

Volumn 117, Issue 1-3, 2009, Pages 42-49

  Esterhuyse, M M ^a   Venter, M ^a   Veldhoen, N ^b   Helbing, C C ^b   van Wyk, J H ^a  

^a STELLENBOSCH UNIVERSITY   (South Africa)

^b UNIVERSITY OF VICTORIA   (Canada)

Author keywords

Development; Oreochromis mossambicus; QPCR; Vitellogenin

Indexed keywords

COMPLEMENTARY DNA; ESTRADIOL; ESTROGEN; ESTROGEN RECEPTOR; GENOMIC DNA; MESSENGER RNA; RNA; VITELLOGENIN;

ADULT ANIMAL; ANIMAL EXPERIMENT; ANIMAL TISSUE; AQUATIC ENVIRONMENT; ARTICLE; BINDING SITE; CONTROLLED STUDY; DNA ISOLATION; ENVIRONMENTAL EXPOSURE; FEMALE; FERTILIZATION; GENE SEQUENCE; HOMOGENATE; JUVENILE ANIMAL; LIVER; MALE; NONHUMAN; NUCLEOTIDE SEQUENCE; ONTOGENY; PROMOTER REGION; PROTEIN EXPRESSION; REAL TIME POLYMERASE CHAIN REACTION; RNA ISOLATION; TILAPIA;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DNA PRIMERS; ENDOCRINE DISRUPTORS; ENVIRONMENTAL MONITORING; ESTRADIOL; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; LIVER; MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; PROMOTER REGIONS, GENETIC; RNA, MESSENGER; SOUTH AFRICA; TILAPIA; VITELLOGENINS;

OREOCHROMIS MOSSAMBICUS;

EID: 70349169829     PISSN: 09600760     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jsbmb.2009.07.001     Document Type: Article

References (71)

1. Krimsky S. Hormonal Chaos: The Scientific and Social Origins of the Environmental Endocrine Hypothesis (2000), The John Hopkins University Press, Baltimore
2. Guillette Jr. L.J., Crain D., Rooney A., and Pickford D. Organization versus activation: the role of endocrine-disrupting contaminants (EDC's) during embryonic development in wildlife. Environmental Health Perspectives 103 (1995) 157-164
3. Cheshenko K., Pakdel F., Segner H., Kah O., and Eggen R.I.L. Interference of endocrine disrupting chemicals with aromatase CYP19 expression or activity, and consequences for reproduction of teleost fish. General and Comparative Endocrinology 155 (2008) 31-62
4. Edwards T.M., and Myers J.P. Environmental exposures and gene regulation in disease etiology (review). Environmental Health Perspectives 115 (2007) 1264
5. Janicke F. Are all aromatase inhibitors the same? A review of the current evidence. The Breast 13 (2004) 10-18
6. Kloas W. Amphibians as a model for the study of endocrine disruptors. International Review of Cytology (2002), Academic Press pp. 1-57
7. Mills L.J., and Chichester C. Review of evidence: are endocrine-disrupting chemicals in the aquatic environment impacting fish populations?. Science of the Total Environment 343 (2005) 1-34
8. Guillette Jr. L.J. Endocrine disrupting contaminants-beyond the dogma. Environmental Health Perspectives 114 (2006) 9-12
9. Jobling S., and Tyler C.R. Endocrine disruption in wild freshwater fish. Pure and Applied Chemistry 75 (2003) 2219-2234
10. Bruton M., and Boltt R. Aspects of the biology of Tilapia mossambica Peters (Pisces: Cichlidae) in a natural freshwater lake (Lake Sibaya, South Africa). Journal of Fish Biology 7 (1975) 423-445
11. Nagahama Y. Endocrine control of oocyte maturation in teleosts. Progress in Clinical Biology Research 342 (1990) 385-392
12. Nagahama Y. Endocrine regulation of gametogenesis in fish. International Journal of Developmental Biology 38 (1994) 217-229
13. Noaksson E., Linderoth M., Bosveld A.T.C., and Balk L. Altered steroid metabolism in several teleost species exposed to endocrine disrupting substances in refuse dump leachate. General and Comparative Endocrinology 134 (2003) 273-284
14. Zhong X., Xu Y., Liang Y., Liao T., and Wang J. The Chinese rare minnow (Gobiocypris rarus) as an in vivo model for endocrine disruption in freshwater teleosts: a full life-cycle test with diethylstilbestrol. Aquatic Toxicology 71 (2005) 85-95
15. Piferrer F., Blazquez M., Navarro L., and Gonzalez A. Genetic, endocrine, and environmental components of sex determination and differentiation in the European sea bass (Dicentrarchus labrax L.). General and Comparative Endocrinology 142 (2005) 102-110
16. Kuhl A.J., Manning S., and Brouwer M. Brain aromatase in Japanese medaka (Oryzias latipes): molecular characterization and role in xenoestrogen-induced sex reversal. The Journal of Steroid Biochemistry and Molecular Biology 96 (2005) 67-77
17. Hahlbeck E., Griffiths R., and Bengtsson B.E. The juvenile three-spined stickleback (Gasterosteus aculeatus L.) as a model organism for endocrine disruption. I. Sexual differentiation. Aquatic Toxicology 70 (2004) 287-310
18. Sharpe R.L., MacLatchy D.L., Courtenay S.C., and Van Der Kraak G.J. Effects of a model androgen (methyl testosterone) and a model anti-androgen (cyproterone acetate) on reproductive endocrine endpoints in a short-term adult mummichog (Fundulus heteroclitus) bioassay. Aquatic Toxicology 67 (2004) 203-215
19. Tao L., Shiwei J., Yang F.X., Yang H., and Ying X. An enzyme-linked immunosorbent assay for rare minnow (Gobiocypris rarus) vitellogenin and comparison of vitellogenin responses in rare minnow and zebrafish (Danio rerio). Science of the Total Environment 364 (2006) 284-294
20. Filby A.L., Thorpe K.L., Maack G., and Tyler C.R. Gene expression profiles revealing the mechanisms of anti-androgen- and estrogen-induced feminization in fish. Aquatic Toxicology 81 (2007) 219-231
21. Helbing C., Gergely G., and Atkinson B.G. Sequential up-regulation of thyroid hormone beta receptor, ornithine transcarbamylase, and carbamyl phosphate synthetase mRNAs in the liver of Rana catesbeiana tadpoles during spontaneous and thyroid hormone-induced metamorphosis. Developmental Genetics 13 (1992) 289-301
22. Zhang F., Degitz S.J., Holcombe G.W., Kosian P.A., Tietge J., Veldhoen N., and Helbing C.C. Evaluation of gene expression endpoints in the context of a Xenopus laevis metamorphosis-based bioassay to detect thyroid hormone disruptors. Aquatic Toxicology 76 (2006) 24-36
23. Segner H., Eppler E., and Reinecke M. The impact of environmental hormonally active substances on the endocrine and immune systems of fish. In: Reinecke M., Zaccone G., and Kapoor B. (Eds). Fish Endocrinology (2006), Science Publishers, Enfield 809-865
24. Hiramatsu N., Cheek A.O., Sullivan C.V., Matsubara T., and Hara A. Vitellogenesis and endocrine disruption. In: Mommsen T.P., and Moon T.W. (Eds). Biochemical and Molecular Biology of Fishes (2007), Elsevier Science BV, Amsterdam 431-471
25. Porte C., Janer G., Lorusso L.C., Ortiz-Zarragoitia M., Cajaraville M.P., Fossi M.C., and Canesi L. Endocrine disruptors in marine organisms: approaches and perspectives. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 143 (2006) 303-315
26. Sumpter J.P., and Jobling S. Vitellogenesis as a biomarker for estrogenic contamination. Environmental Health Perspectives Supplements 103 Suppl. 7 (1995) 173
27. Lim E.H., Ding J.L., and Lam T.J. Estradiol-induced vitellogenin gene expression in a teleost fish, Oreochromis aureus. General and Comparative Endocrinology 82 (1991) 206-214
28. Harries J.E., Sheahan D.A., Jobling S., Matthiessen P., Neall P., Routledge E.J., Rycroft R., Sumpter J.P., and Tylor T. A survey of estrogenic activity in United Kingdom inland waters. Environmental Toxicology and Chemistry 15 (1996) 1993-2002
29. Thorpe K.L., Benstead R., Hutchinson T.H., and Tyler C.R. Associations between altered vitellogenin concentrations and adverse health effects in fathead minnow (Pimephales promelas). Aquatic Toxicology 85 (2007) 176-183
30. Jobling S., Nolan M., Tyler C.R., Brighty G., and Sumpter J.P. Widespread sexual disruption in wild fish. Environmental Science & Technology 32 (1998) 2498-2506
31. Kim B.H., Takemura A., Kim S.J., and Lee Y.D. Vitellogenin synthesis via androgens in primary cultures of tilapia hepatocytes. General and Comparative Endocrinology 132 (2003) 248-255
32. Takemura A., and Kim B.H. Effects of estradiol-17[beta] treatment on in vitro and in vivo synthesis of two distinct vitellogenins in tilapia. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 129 (2001) 641-651
33. Miracle A., Ankley G., and Lattier D. Expression of two vitellogenin genes (vg1 and vg3) in fathead minnow (Pimephales promelas) liver in response to exposure to steroidal estrogens and androgens. Ecotoxicology and Environmental Safety 63 (2006) 337-342
34. Vaillant C., Le Guellec C., Pakdel F., and Valotaire Y. Vitellogenin gene expression in primary culture of male rainbow trout hepatocytes. General and Comparative Endocrinology 70 (1988) 284-290
35. Craft J.A., Brown M., Dempsey K., Francey J., Kirby M.F., Scott A.P., Katsiadaki I., Robinson C.D., Davies I.M., Bradac P., and Moffat C.F. Kinetics of vitellogenin protein and mRNA induction and depuration in fish following laboratory and environmental exposure to oestrogens. Marine Environmental Research 58 (2004) 419-423
36. Arukwe A., Celius T., Walther B.T., and Goksoyr A. Plasma levels of vitellogenin and eggshell zona radiata proteins in 4-nonylphenol and o,p'-DDT treated juvenile Atlantic salmon (Salmo salar). Marine Environmental Research 46 (1998) 133-136
37. Kordes C., Rieber E.P., and Gutzeit H.O. An in vitro vitellogenin bioassay for oestrogenic substances in the medaka (Oryzias latipes). Aquatic Toxicology 58 (2002) 151-164
38. Zhang Z.B., Hu J.Y., An W., Jin F., An L.H., Tao S., and Chen J.S. Induction of vitellogenin mRNA in juvenile Chinese sturgeon (Acipenser sinensis Gray) treated with 17 beta-estradiol and 4-nonylphenol. Environmental Toxicology and Chemistry 24 (2005) 1944-1950
39. Trewavas E. Tilapiine Fishes (1983), British Museum, London
40. Popma T., and Masser M. Tilapia: Life History and Biology 283 (1999), SRAC Publication
41. Neil E. Observations on the behaviour of Tilapia mossambica (Pisces, Cichlidae) in Hawaiian ponds. Copeia 1996 (1966) 50-56
42. Wright J.M. Nucleotide sequence, genomic organization and evolution of a major repetitive DNA family in tilapia (Oreochromis mossambicus/honorum). Nucleic Acids Research 17 (1989) 5071-5079
43. Wohlfarth G.W., and Wedekind H. The heredity of sex determination in tilapias. Aquaculture 92 (1991) 143-156
44. Wang L.H., and Tsai C.L. Temperature affects the development of central neurotransmitter systems of tilapia, Oreochromis mossambicus. Neuroscience Letters 285 (2000) 95-98
45. Vijayan M.M., Takemura A., and Mommsen T.P. Estradiol impairs hyposmoregulatory capacity in the euryhaline tilapia, Oreochromis mossambicus. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 281 (2001) R1161-R1168
46. Tsai C.L., and Wang L.H. Effects of thermal acclimation on the neurotransmitters, serotonin and norepinephrine in the discrete brain of male and female tilapia, Oreochromis mossambicus. Neuroscience Letters 233 (1997) 77-80
47. Schmid A.C., Lutz I., Kloas W., and Reinecke M. Thyroid hormone stimulates hepatic IGF-I mRNA expression in a bony fish, the tilapia Oreochromis mossambicus, in vitro and in vivo. General and Comparative Endocrinology 130 (2003) 129-134
48. Nussey G., Van Vuren J.H.J., and du Preez H.H. Effect of copper on the haematology and osmoregulation of the Mozambique tilapia, Oreochromis mossambicus (Cichlidae). Comparative Biochemistry and Physiology Part C: Comparative Pharmacology and Toxicology 111 (1995) 369-380
49. Majumdar K., and McAndrew B. Relative DNA content of somatic nuclei and chromosomal studies in three genera, Tilapia, Sarotherodon, and Oreochromis of the tribe Tilapiini (Pisces, Cichlidae). Genetica 68 (1986) 175-188
50. D'Amato M., Esterhuyse M., Van der Waal B., Brink D., and Volckaert F. Hybridization and phylogeography of the Mozambique tilapia Oreochromis mossambicus in southern Africa evidenced by mitochondrial and microsatellite DNA genotyping. Conservation Genetics 8 (2007) 475-488
51. Chang X., Kobayashi T., Senthilkumaran B., Kobayashi-Kajura H., Sudhakumari C.C., and Nagahama Y. Two types of aromatase with different encoding genes, tissue distribution and developmental expression in Nile tilapia (Oreochromis niloticus). General and Comparative Endocrinology 141 (2005) 101-115
52. Gussow D., and Clackson T. Direct clone characterization from plaques and colonies by the polymerase chain reaction. Nucleic Acids Research 17 (1989) 4000
53. Chenna R., Sugawara H., Koike T., Lopez R., Gibson T.J., Higgins D.G., and Thompson J.D. Multiple sequence alignment with the Clustal series of programs. Nucleic Acids Research 31 (2003) 3497-3500
54. Hall T. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids, Symposium Series, vol. 41 (1999) 95-98
55. Ochman H., Gerber A., and Hartl D. Genetic applications of an inverse polymerase chain reaction. Genetics 120 (1988) 621-623
56. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research 29 (2001) e45
57. Kubista M., Andrade J.M., Bengtsson M., Forootan A., Jonak J., Lind K., Sindelka R., Sjoback R., Sjogreen B., and Strombom L. The real-time polymerase chain reaction. Molecular Aspects of Medicine 27 (2006) 95-125
58. Bustin S. Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems. Journal of Molecular Endocrinology 29 (2002) 23-39
59. Rutledge R., and Côte C. Mathematics of quantitative kinetic PCR and the application of standard curves. Nucleic Acids Research 31 (2003) E93
60. Teo B.Y., Tan N.S., Lim E.H., Lam T.J., and Ding J.L. A novel piscine vitellogenin gene: structural and functional analyses of estrogen-inducible promoter. Molecular and Cellular Biology 146 (1998) 103-120
61. Davis L.K., Hiramatsu N., Hiramatsu K., Reading B.J., Matsubara T., Hara A., Sullivan C.V., Pierce A.L., Hirano T., and Grau E.G. Induction of three vitellogenins by 17beta-estradiol with concurrent inhibition of the growth hormone-insulin-like growth factor 1 axis in a euryhaline teleost, the Tilapia (Oreochromis mossambicus). Biology of Reproduction 77 (2007) 614-625
62. Hardison R. Conserved noncoding sequences are reliable guides to regulatory elements. Trends in Genetics 16 (2000) 369-372
63. Loots G., Ovcharenko I., Pachter L., Dubchak I., and Rubin E. rVista for comparative sequence-based discovery of functional transcription factor binding sites. Genome Research 12 (2002) 832-839
64. Teo B.Y., Tan N.S., Lam T.J., and Ding J.L. Synergistic effects of nuclear factors-GATA, VBP and ER in potentiating vitellogenin gene transcription. FEBS Letters 459 (1999) 57-63
65. Lam S., Mathavan S., Tong Y., Li H., Karuturi R., Wu Y., Vega V., Liu E., and Gong Z. Zebrafish whole-adult-organism chemogenomics for large-scale predictive and discovery chemical biology. PLoS Genetics 4 (2008) e1000121
66. Clemens H., and Inslee T. The production of unisex broods by Tilapia mossambica sex-reversed with methyltestosterone. Transactions of the American Fisheries Society 97 (1968) 18-21
67. Ding J.L., Hee P.L., and Lam T.J. Two forms of vitellogenin in the plasma and gonads of male Oreochromis aureus. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 93 (1989) 363-370
68. Ding J., Ng W., Lim E., and Lam T. In situ hybridization shows the tissue distribution of vitellogenin gene expression in Oreochromis aureus. Cytobios 73 (1993) 294-295
69. Mikawa N., Utoh T., Horie N., Okamura A., Yamada Y., Akazawa A., Tanaka S., Tsukamoto K., Hirono I., and Aoki T. Cloning and characterization of vitellogenin cDNA from the common Japanese conger (Conger myriaster) and vitellogenin gene expression during ovarian development. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 143 (2006) 404-414
70. Gordon D.A., Toth G.P., Graham D.W., Lazorchak J.M., Reddy T.V., Knapp C.W., deNoyelles J., Campbell S., and Lattier D.L. Effects of eutrophication on vitellogenin gene expression in male fathead minnows (Pimephales promelas) exposed to 17[alpha]-ethynylestradiol in field mesocosms. Environmental Pollution 142 (2006) 559-566
71. Scholz S., Kordes C., Hamann J., and Gutzeit H.O. Induction of vitellogenin in vivo and in vitro in the model teleost medaka (Oryzias latipes): comparison of gene expression and protein levels. Marine Environmental Research 57 (2004) 235-244