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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/24976
Title: Function and Regulation of Fish CYP3 Genes
Other Titles: Characterizing the Function and Regulation of Orphan CYP3 Genes in Zebrafish (Danio Rerio)
Authors: Shaya, Lana
Advisor: Wilson, Joanna Y.
Department: Biology
Keywords: Cytochrome P450;function of orphan CYPs;regulation of cytochrome P450s;CYP3C1;CYP3A65;xenobiotic metabolism;zebrafish;pharmaceutical metabolism;high throughput screening;Aryl hydrocarbon receptor;Estrogen Receptor
Publication Date: 2019
Abstract: Genome sequencing has resulted in the identification of >55,000 cytochrome P450 enzymes, many of which have an unknown function and regulation. In mammals, CYP3 genes appear in only one subfamily (CYP3A), which metabolize >50% of pharmaceuticals and some steroids in humans. Unlike mammals, fish contain genes in the CYP3A, CYP3B, CYP3C and CYP3D subfamilies. While it is commonly assumed that fish and mammalian CYP3A are functional similar, the function and regulation of fish CYP3 remains largely unknown. In this thesis, the receptors and compounds that regulate CYP3C genes in zebrafish were assessed. The induction of CYP3C genes in response to the aryl hydrocarbon (AHR) and estrogen receptor (ER) ligands, β-naphthoflavone and 17β-estradiol, was measured using quantitative PCR in intestine, liver and gonads. Zebrafish CYP3C genes were inducible by β-naphthoflavone and 17β-estradiol, implicating the aryl hydrocarbon and estrogen receptor in CYP3C gene regulation and suggesting that regulation of CYP3 genes in fish differs from that in mammals. To define the function of zebrafish CYP3A65 and CYP3C1, fluorogenic compounds which are specific markers of CYP1 and CYP3A activity in humans, were screened for metabolism by CYP3A65 and CYP3C1. Both CYP3A65 and CYP3C1 had the capacity to metabolize several of these compounds and the substrate profile overlapped with zebrafish CYP1A, suggesting that these compounds are not specific in fish. A high throughput approach was employed to screen ~4000 small biologically and pharmacologically active compounds for metabolism by CYP3A65 and CYP3C1, using NADPH consumption to assess catalytic activity. The substrate profiles of CYP3A65 and CYP3C1 largely overlapped and were different than mammalian CYP3A4. CYP3A65 and CYP3C1 appeared to have a bias for quinone-based compounds but further studies are required to confirm quinones as substrates and to assess a strong structure-activity relationship. Overall, this study provides insight on the regulation, function and evolution on CYP3 genes in fish.
URI: http://hdl.handle.net/11375/24976
Appears in Collections:Open Access Dissertations and Theses

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Ph.D. Dissertation - Characterizing cytochrome P450 family 3 genes in zebrafish7.27 MBAdobe PDFView/Open
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