P. Smith et al., EFFECTS OF THE BOOROOLA GENE (FECB(B)) ON BODYMASS, TESTIS DEVELOPMENT AND HORMONE CONCENTRATIONS DURING FETAL LIFE, Journal of Reproduction and Fertility, 108(2), 1996, pp. 253-261
In female fetuses the Booroola gene (FecB(B)) is known to affect germ
cell development and consequently the pattern of ovarian follicular gr
owth during fetal and post-natal life. However in males, the role of t
his gene during fetal development is unknown. The aims of the study re
ported here were to examine the effects of the FecB(B) gene on develop
ment of male fetuses with respect to body and organ mass (for example,
pituitary gland, adrenal and mesonephros), testes development, includ
ing numbers of germ cells, and also the plasma concentrations or tissu
e contents of the reproductive hormones (FSH, LH and testosterone) at
days 40, 55, 75, 90 and 135 of gestation. The FecB(B) gene was found t
o influence litter size, bodymass, crown-rump length and testis mass a
t most stages of gestation. Some effects were also noted on the mesone
phros at days 40 and 55 and on the pituitary and adrenal at days 90 or
135 of gestation. However, the FecB(B) gene was not observed to have
an effect on the patterns of germ cell development, on pituitary conte
nt or plasma concentrations of immunoreactive or bioactive FSH or immu
noreactive LH or testicular content of testosterone. When embryo trans
fer experiments were performed to eliminate the effects of litter size
at days 40, 90 and 135 of gestation nearly all of the differences in
bodymass, crown-rump length and organ mass disappeared. The only excep
tion to this was at day 90 when bodymass continued to be lighter and c
rown-rump lengths smaller in the BB/B + fetuses compared with the ++ f
etuses; the significance of this finding remains unknown. It is conclu
ded that for Booroola male fetuses there are no direct effects of the
FecB(B) gene on pituitary gonadotrophin function or testicular develop
ment after sexual differentiation. Moreover, although there may be tem
poral differences around day 90 of gestation, there are no long-term,
direct effects of the FecB(B) gene on total body, adrenal, testis or p
ituitary mass. Collectively these findings for the male are similar to
those for female fetuses except with regard to germ cell development.