Promoter characteristics of two cyp19 genes differentially expressed in the brain and ovary of teleost fish

Teleost fish are characterized by exceptionally high levels of neural estrogen biosynthesis when compared with the brains of other vertebrates or to the ovaries of the same fish. Two P450arom mRNAs which derive from separate gene loci ( cyp19a and cyp19b) are differentially expressed in brain (b≫a) and ovary (a≫b) and have a different developmental program (b≫a) and estrogen upregulation (b only). A polymerase chain reaction (PCR)-based genomic walking strategy was used to isolate the 5′-flanking regions of the goldfish ( Carassius auratus) cyp19 genes. Sequence analysis of the cyp19b gene ∼1.8 kb upstream of the transcription start site revealed a TATA box at nucleotide (nt) −30, two estrogen responsive elements (EREs; nt −351 and −211) and a consensus binding site (NBRE) for nerve growth factor inducible-B protein (NGFI-B/Nur77) at −286, which includes another ERE half-site. Also present were a sequence at nt −399 (CCCTCCT) required for neural specificity of the zebrafish GATA-2 gene, and 16 copies of an SRY/SOX binding motif. The 5′-flanking region (∼1.0 kb) of the cyp19a gene had TATA (nt −48) and CAAT (nt −71) boxes, a steroidogenic factor-1 (SF-1) binding site (nt −265), eight copies of the SRY/SOX motif, and two copies of a recognition site for binding the arylhydrocarbon receptor (AhR)/AhR nuclear translocator factor (ARNT) heterodimer. Both genes had elements previously identified in the brain specific exon I promoter of the mouse aromatase gene. Cyp19a- and - b/luciferase constructs showed basal promoter activity in aromatase-expressing rodent pituitary (GH3) cells, but differences (a≫b) did not reflect expression in fish pituitary in vivo (b≫a), implying a lack of appropriate cell factors. Consistent with the onset of cyp19b expression in zebrafish embryos, microinjection of a green fluorescent protein (GFP) reporter plasmid into fertilized eggs revealed labeling in neural tissues at 30–48 h post-fertilization (hpf), most prominently in retinal ganglion cells (RGC) and axon-like projections to the optic tectum. Expression of a cyp19a/GFP reporter was not detectable up to 72 hpf. Tandem analysis of cyp19a and cyp19b promoters in living zebrafish embryos can be a useful approach for identifying cis-elements and cellular factors involved in the correct tissue-specific, spatial, temporal and estrogen regulated expression of aromatase genes during CNS and gonadal development.