Abstract
CYP11A1 encodes the first enzyme of steroid biosynthesis, cytochrome P450scc. The expression of CYP11A1 in the nervous system allows neurosteroids to be synthesized de novo. In the classic steroidogenic tissues, adrenals and gonads, the key regulator controlling CYP11A1 expression is steroidogenic factor‐1 (SF‐1), but the transcriptional regulation of CYP11A1 in the brain is unclear. We recently used the 4.4‐kb regulatory region of the human CYP11A1 gene to drive Cre recombinase expression in the diencephalon and midbrain. In this study, we characterized the regional‐specific expression of Cre reporter in the SCC‐Cre transgenic brain using a transient Cre/ROSA26R transgenic system. Mutation of either the upstream or proximal SF‐1 binding site did not affect brain CYP11A1 promoter activity. The upstream SF‐1 binding site, however, is required for CYP11A1 promoter function in the embryonic adrenals. The 3.8‐kb promoter, like the 4.4‐kb length promoter, directed Cre expression in the diencephalon, midbrain and olfactory epithelium, whereas Cre expression controlled by the 2.7‐kb promoter was only observed in the caudal part of midbrain. This suggests that the 5′‐flanking region between 3.8 and 2.7 kb contains a crucial element for activation of CYP11A1 promoter in the diencephalon, olfactory epithelium and the anterior part of midbrain. Thus we have identified regions of the promoter that control CYP11A1 expression in the brain and embryonic adrenals. J. Cell. Physiol. 226: 1998–2005, 2011. © 2010 Wiley‐Liss, Inc.