M. Govoroun et al., Steroid enzyme gene expressions during natural and androgen-induced gonadal differentiation in the rainbow trout, Oncorhynchus mykiss, J EXP ZOOL, 290(6), 2001, pp. 558-566
In fish, according to Yamamoto's model, androgens would drive testis differ
entiation and estrogens ovarian differentiation. In order to study the impl
ication of steroid enzymes in rainbow trout gonadal differentiation, we exa
mined the expression of some steroid enzyme genes during natural differenti
ation (cholesterol side chain cleavage = P450scc, 17-hydroxylase/lyase = P4
50c17, 3 beta -hydroxysteroid dehydrogenase = 3 beta HSD) and androgen-indu
ced differentiation (P450scc, P450c17, 3 beta HSD, aromatase = P450aro, and
11 beta -hydroxylase = P45011 beta). Expressions of P450scc, 3 beta HSD, a
nd P450c17 were all detected in male and female gonads at 55 days post-fert
ilization (dpf), i.e., two weeks before histological differentiation. There
were no differences in their expression level respective to the sex. The a
ndrogen treatment was carried out by administration of 11 beta -hydroxyandr
ostenedione (11 beta OH Delta4) in genetic all-female populations and the r
esulting sex ratios were found to be 100% male even at a low dosage of 1 mg
/kg of food. Following 11 beta OH Delta4 treatment, only the expression of
P450c17 was found to be sustained when compared with the female untreated c
ontrol. In contrast, P450scc was clearly up-regulated and 3 beta HSD and P4
50aro down-regulated by the androgen treatment. P45011 beta gene expression
remained low in gonads of androgen-treated females, as it did in control u
ntreated females. These results together demonstrate that steroidogenesis i
n rainbow trout is potentially active in predifferentiating gonads of both
sexes, and that one of the masculinizing actions of androgens in the specie
s may be to down-regulate the female-specific gonadal P450aro gene expressi
on. However, in vivo androgen treatment in genetic females does not induce
the same pattern of steroid gene expression as in genetic males. These data
suggest that exogenous androgens might induce a male differentiation proce
ss with P450aro inhibition being one of the steps required. However, this p
rocess would not involve endogenously produced 11-oxygenated androgens. J.
Exp. Zool. 290:558-566, 2001. (C) 2001 Wiley-Liss, Inc.