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Impact of environmental estrogens on nucleotide excision repair gene expression in embryonic zebrafish

Notch, Emily G., Mayer, Gregory D.
Comparative Biochemistry and Physiology, Part C 2013 v.157 pp. 361-365
DNA repair, Danio rerio, adults, aquatic environment, endocrine-disrupting chemicals, environmental impact, estrone, fauna, gene expression, genes, hormone replacement therapy, messenger RNA, metabolites, oral contraceptives, transcription (genetics), vitellogenin, xenoestrogens
Estrogens and estrogen mimics are aquatic contaminants that can elicit a variety of deleterious effects in exposed fauna. One of the most potent xenoestrogens found in the aquatic environment is 17α-ethinylestradiol (EE2), the pharmaceutically derived semi-synthetic hormone found in oral contraceptives and hormone replacement therapies. Exposure to 100ng/L EE2 has previously been shown to profoundly decrease functional hepatic nucleotide excision repair (NER) processes in adult zebrafish in correlation with dramatic decreases in the abundance of hepatic XPC and XPA transcripts; however, its effects on these processes in embryos are currently unknown. Because developing organisms are known to have increased sensitivities to endocrine disrupting compounds such as EE2, the goal of this study was to examine the impacts of estrogen exposure on mRNA expression of these two key NER genes in zebrafish embryos during the first 4 days of development. Embryos were exposed from 0h post fertilization (hpf) to waterborne EE2, its major metabolite, estrone (E1), or combinations of the two compounds and sampled at 12, 24, 48, 72 and 96 hpf. Increased abundance of vitellogenin-1 (VTG1) mRNA, a bioindicator of estrogen exposure, was evident as early as 24 hpf in embryos that were co-exposed to EE2 and E1 and this effect was sustained throughout 96 hpf. Embryos exposed to EE2 alone exhibited elevated VTG1 beginning at 72 hpf. In contrast to observations from adult zebrafish exposed to EE2, embryos did not show any change in mRNA abundance of the excision repair gene, XPC, during the first 4days of development. However, co-exposure to EE2 and E1 elicited an increase in XPA mRNA abundance at 48 and 72 hpf, which was the opposite response as that observed in exposed adults where hepatic XPA mRNA abundance decreased after EE2 exposure. These differences between embryos and adults suggest that alteration of NER gene transcription by EE2 is operating under different stimuli during development.