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Journal of Endocrinology (2009) 202, 99-109       DOI: 10.1677/JOE-08-0353
© 2009 Society for Endocrinology
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Role of DNA methylation in the tissue-specific expression of the CYP17A1 gene for steroidogenesis in rodents

Elika Missaghian1,*, Petra Kempná1, Bernhard Dick2, Andrea Hirsch1, Rasoul Alikhani-Koupaei2, Bernard Jégou3, Primus E Mullis1, Brigitte M Frey2 and Christa E Flück1

1 Pediatric Endocrinology and Diabetology, University Children's Hospital Bern
2 Department of Nephrology and Hypertension, Inselspital, University of Bern, Freiburgstrasse 15, Room G3 812, CH-3010 Bern, Switzerland
3 Inserm, U625, GERHM, IFR140, Université de Rennes 1, Campus de Beaulieu, Rennes Cedex F-35042, France

(Correspondence should be addressed to C E Flück; Email: christa.flueck{at}dkf.unibe.ch)

* (Elika Missaghian has previously published under the name Elika Samandari)

The CYP17A1 gene is the qualitative regulator of steroidogenesis. Depending on the presence or absence of CYP17 activities mineralocorticoids, glucocorticoids or adrenal androgens are produced. The expression of the CYP17A1 gene is tissue as well as species-specific. In contrast to humans, adrenals of rodents do not express the CYP17A1 gene and have therefore no P450c17 enzyme for cortisol production, but produce corticosterone. DNA methylation is involved in the tissue-specific silencing of the CYP17A1 gene in human placental JEG-3 cells. We investigated the role of DNA methylation for the tissue-specific expression of the CYP17A1 gene in rodents. Rats treated with the methyltransferase inhibitor 5-aza-deoxycytidine excreted the cortisol metabolite tetrahydrocortisol in their urine suggesting that treatment induced CYP17 expression and 17{alpha}-hydroxylase activity through demethylation. Accordingly, bisulfite modification experiments identified a methylated CpG island in the CYP17 promoter in DNA extracted from rat adrenals but not from testes. Both methyltransferase and histone deacetylase inhibitors induced the expression of the CYP17A1 gene in mouse adrenocortical Y1 cells which normally do not express CYP17, indicating that the expression of the mouse CYP17A1 gene is epigenetically controlled. The role of DNA methylation for CYP17 expression was further underlined by the finding that a reporter construct driven by the mouse –1041 bp CYP17 promoter was active in Y1 cells, thus excluding the lack of essential transcription factors for CYP17 expression in these adrenal cells.







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