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Identification and Characterization of Androgen-Responsive Genes in Zebrafish Embryos
E. Fetter, S. Smetanová, L. Baldauf, A. Lidzba, R. Altenburger, A. Schüttler, S. Scholz,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Receptors, Androgen genetics MeSH
- Androgens genetics metabolism MeSH
- Androgen Antagonists pharmacology MeSH
- Zebrafish embryology genetics MeSH
- Embryo, Nonmammalian drug effects MeSH
- Ethinyl Estradiol pharmacology MeSH
- Gene Expression drug effects MeSH
- Imidazolidines pharmacology MeSH
- Humans MeSH
- Gene Expression Profiling MeSH
- Testosterone analogs & derivatives pharmacology MeSH
- Gene Expression Regulation, Developmental drug effects MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Responsive genes for fish embryos have been identified so far for some endocrine pathways but not for androgens. Using transcriptome analysis and multiple concentration-response modeling, we identified putative androgen-responsive genes in zebrafish embryos exposed to 0.05-5000 nM 11-ketotestosterone for 24 h. Four selected genes with sigmoidal concentration-dependent expression profiles (EC50 = 6.5-30.0 nM) were characterized in detail. The expression of cyp2k22 and slco1f4 was demonstrated in the pronephros; lipca was detected in the liver, and sult2st3 was found in the olfactory organs and choroid plexus. Their expression domains, the function of human orthologs, and a pathway analysis suggested a role of these genes in the metabolism of hormones. Hence, it was hypothesized that they were induced to compensate for elevated hormone levels. The induction of sult2st3 and cyp2k22 by 11-ketotestosterone was repressed by co-exposure to the androgen receptor antagonist nilutamide supporting a potential androgen receptor mediated regulation. Sensitivity (expressed as EC50 values) of sult2st3 and cyp2k22 gene expression induction after exposure to other steroidal hormones (11-ketotestosterone ∼ testosterone > progesterone > cortisol > ethinylestradiol) correlated with their known binding affinities to zebrafish androgen receptor. Hence, these genes might represent potential markers for screening of androgenic compounds in the zebrafish embryo.
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