Journal of Fisheries Science and Technology

Journal of Fisheries Science and Technology

DNA methylation in liver and ovary tissues of Caspian Kutum broodstock and embryos (Rutilus Kutum) under genistein and β-sitosterol exposures

Document Type : Original Research

Authors
1 Fisheries Department, Natural Resources & Environmental Faculty, Malayer University, Malayer, Iran
2 Fisheries Department, Natural Resources Faculty, University of Tehran, Karaj, Iran
Abstract
Aims: A wide range of chemical endocrine disrupters modifies DNA methylation. Like a weak class of estrogens, phytoestrogens can affect aquatic animal reproduction and disturb the structure of endocrine systems.

Materials and Methods: In order to study the epigenetic effects of genistein and β-sitosterol, 49 female adults (for about 21 days) and fertilized eggs (until hatching time) of Kutum’s exposed to 3 different levels of genistein and β-sitosterol (10, 50, 500ng/l). At the end, the liver, the ovaries, and embryos were sampled and methylation-sensitive amplified polymorphism (MSAP) was used to evaluate the level of DNA methylation.

Findings: According to result the fish exposed to high level of β-sitosterol shown hypo DNA methylation in the liver. Compared with control, both of these compounds could effect on the ovary and embryos DNA methylation pattern. The result showed, whole genome methylation had a different pattern in the liver, ovary, and embryos, which treated by 500ng/l of β-sitosterol.

Conclusion: Methylation change pattern can be changed depends on the type of tissue and structure and level of the phytoestrogen compounds. According to this study, genistein and β-sitosterol could affect reproduction and embryo development by changing molecular indices. It seems that these compounds could affect the endocrine system of Kutum and reduce reproduction performance of Kutum in the long period.
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Aluru, N., Leatherland, JF and Vijayan, MM. 2010. Bisphenol A in Oocytes Leads to Growth Suppression and Altered Stress Performance in Juvenile Rainbow Trout. PLoS ONE, 5(5): e10741.
Aniagu, S.O., Williams, T.D., Allen, Y., Katsiadaki, I. and Chipman, J.K. 2008. Global genomic methylation levels in the liver and gonads of the three-spine stickleback (Gasterosteus aculeatus) after exposure to hexabromocyclododecane and 17-beta oestradiol. Environ. Int, 34: 310–317.
Cederroth, C.R., Zimmermann, C. and Nef, S. 2012. Soy, phytoestrogens and their impact on reproductive health, "Review". Molecular and Cellular Endocrinology, 355: 192–200.
Contractor, R.G., Foran, C.M., Li, S. and Willett, K.L. 2004. Evidence of gender- and tissue specific promoter methylation and the potential for ethinylestradiol-induced changes in Japanese medaka (Oryzias latipes) estrogen receptor and aromatase genes. J. Toxicol. Environ. Health A, 67:1–22.
Covelo-Soto, L., Saura, M. and Morán, P. 2015. Does DNA methylation regulate metamorphosis? The case of the sea lamprey (Petromyzon marinus) as an example. Comp.Biochem. Physiol., Part B Biochem. Mol. Biol, 185:42–46.
Ding, Y., He, F., Wen, H., Li, J., Ni, M., Chi, M., Qian, K., Bu, Y., Zhang, D., Si, Y. and Zhao J. 2013. DNA methylation status of cyp17-II gene correlated with its expression pattern and reproductive endocrinology during ovarian development stages of Japanese flounder (Paralichthys olivaceus). Gene, 527: 82–88.
Fulneček, J. and Kovařík, A. 2014. How to interpret Methylation Sensitive Amplified Polymorphism (MSAP) profiles? BMC Genetics, 15:2.
Head, A. J. 2014. Patterns of DNA Methylation in Animals: An Ecotoxicological Perspective. Integrative and Comparative Biology, 54(1):77–86.
Herceg, Z. and Vaissiere, T. 2011. Epigenetic mechanisms and cancer: an interface between the environment and the genome.Epigenetics, 6:804–819.
Jafari, M., Kamarudin, M.S., Saad, CH.R, Arshad, A., Oryan, SH. and Bahmani, M. 2009. Development of morphology in hatchery- reared Rutilus frissi kutum Larvae. Eur. J.Sci. Res. 38(2), 296-305.
Jeltsch, A., Jurkowska, R. Z., Jurkowski, T.P., Liebert, K., Rathert, P and Schlickenrieder, M. 2007. Application of DNA methyltransferases in targeted DNA methylation. Appl. Microbiol. Biotechnol. 75:1233– 1240.
Kiparissis, Y., Balch, G.C., Metcalfe, T. L. and Metcalfe, C.D. 2003. Effects of the Isoflavones Genistein and Equol on the Gonadal Development of Japanese Medaka (Oryzias latipes). Environmental Health Perspect, 111 (9): 1158–1163.
Klose, R and Bird, A .2006. Genomic DNA methylation: the mark and its mediators. Trends in Biochemical Sciences. 31(2): 89-97.
Kuster, M., Azevedo, D.A., López de Alda, M.J., Aquino Neto, F.R. and Barceló, D. 2009. Analysis of phytoestrogens, progestogens and estrogens in environmental waters from Rio de Janeiro (Brazil). Environment International, 35:997–1003
Li, M and Leatherland, F. J. 2013. The implications for aquaculture practice of epigenomic programming of components of the endocrine system of teleost an embryos: lessons learned from mammalian studies. F I SH and F I SHERI E S, 14:528–553.
Liney, K. E., Jobling, S., Shears, J. A., Simpson, P. and Tyler, C. R. 2005. Assessing the sensitivity of different life stages for sexual disruption in roach (Rutilus rutilus) exposed to effluents from wastewater treatment works. Environ. Health Perspect. 113, 1299–1307.
Liu, Y., Yuan, C., Chen, S., Zheng, Y., Zhang, Y., Gao, J. and Wang, Z. 2014. Global and cyp19a1a gene specific DNA methylation in gonads ofadult rare minnow Gobiocypris rarus under bisphenol A exposure. Aquatic Toxicology, 156:10–16.
Liu, Y., Zhang, Y., Tao, S., Guan, Y., Zhang, T. and Wang, Z. 2016. Global DNA methylation in gonads of adult zebra fish Danio rerio under bisphenol A exposure. Ecotoxicology and Environmental Safety, 130:124–132.
Matthews, J., Celius, T., Halgren, R. and Zacharewski, T. 2000. Differential estrogen receptor binding of estrogenic substances: a species comparison. Journal of Steroid Biochemistry and Molecular Biology, 74: 223-234.
Mimura, J and Fujii-Kuriyama, Y. 2003. Functional role of AhR in the expression of toxic effects by TCDD. Biochim. Biophys. Acta 1619: 263-268.
Mohamadian, F., mahmoodi, M., mirzae, M., khoshdel, A., sheikh fathollahi, M. and zeinodini, N. 2015. Expression of Some Genes Involved in Epigenetic in Breast Cancer Cell Lines: The Effect of Quercetin. J Fasa Univ Med Sci.; 5 (3):413-424.
Morán, P. and Pérez-Figueroa, A. 2011. Methylation changes associated with early maturation stages in the Atlantic salmon. BMC Genetics 12:86.
Morán, P., Marco-Rius, F., Megías, M., Covelo-Soto, L. and Pérez-Figueroa, A. 2013. Environmental induced methylation changes associated with seawater adaptation in brown trout. Aquaculture, 392–395: 77–83.
Orrego, R., Guchardi, J., Krause, R. and Holdway, D. 2010. Estrogenic and anti-estrogenic effects of wood extractives present in pulp and paper mill effluents on rainbow trout. Aquatic Toxicology, 99:160–167.
Pluta, HJ. 1993. Investigations on biotransformation (mixed function oxygenase activities) in fish liver. Heidelberg, Germany, Sept. 25 to Sept. 27, 1991. Fish: Ecotoxicology and Ecophysiology. Proceedings of an International Symposium.
Potok, M.E., Nix, D.A., Parnell, T.J. and Cairns, B.R. 2013. Reprogramming the maternal zebrafish genome after fertilization to match the paternal methylation pattern. Cell 153:759–772.
Sassi-Messai, S., Gilbert, Y., Bernard, L., Nishio, S.-I., Lagneu, K.F.F., Molina, J., Anderson-Lendahl, M., Benoit, G., Balaguer, P. and Laudet, V. 2009. The Phytoestrogen Genistein Affects Zebrafish Development through Two Different Pathways. PLoS ONE, 4(3): e4935.
Sharif pour, A., Soltani, M., Abdolhay, H. and Ghayumi, R. 2002. Anesthetic effect of clove extract (Eugenia caryophyllata) at different pH and temperature conditions on common carp juvenile. Iranian fisheries journal, 15(4):59-73.
Stevenson, M. L., C. Brown, A., M. Montgomery, T. and D. Clotfelter, E. 2011. Reproductive Consequences of Exposure to Waterborne Phytoestrogens in Male Fighting Fish Betta splendens. Arch Environ Contam Toxicol, 60:501–510.
Strauss, L., Makela, S., Joshi, S., Huhtaniemi, I and Santti, R. 1998. Genistein exerts estrogen-like effects in male mouse reproductive tract. Mol. Cell. Endocrinol, 144:83–93.
Whyte, J. J. Jung, R. E. Schmitt, C. J. and Tillitt, D. E. 2000. Ethoxyresorufin-Odeethylase (EROD) Activity in Fish as a Biomarker of Chemical Exposure, Critical Reviews in Toxicology, 30(4):347-570.
Xing, H., Wang, C., Wu, H., Chen, D., Li, S. and Xu, S. 2015. Effects of atrazine and chlorpyrifos on DNA methylation in the brain and gonad of the common carp. Comparative Biochemistry and Physiology, Part C, 168:11–19.
Yeoh, C. G., Schreck, C.B., Fitzpatrick, M.S. and Feist, G.W. 1996. In vivo steroid metabolism in embryonic and newly hatched steelhead trout (Oncorhynchus mykiss). Gen. Comp. Endocrinol. 102, 197–209.
Ze-hua, L., Yoshinori, K. and Satoshi, M. 2010. A review of phytoestrogens: Their occurrence and fate in the environment. Water reserch, 44:567 – 577.