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Abstract
In the present study, we cloned and characterized
zebrafish FSH receptor (Fshr) and LH receptor (Lhr). Both
fshr and lhr were abundantly expressed in
the zebrafish
gonads; however, they could also be detected in the kidney
and liver, respectively. When over-expressed in mammalian
cell lines together with a cAMP-responsive reporter gene,
zebrafish Fshr responded to goldfish pituitary extract but
not hCG, whereas Lhr could be activated by both. It was
further demonstrated that Fshr was specific to bovine FSH,
while Lhr could be stimulated by both bovine FSH and LH.
Low level of fshr expression could be detected in the
immature ovary, but the level steadily increased during
vitellogenesis of the first cohort of developing
follicles. In contrast, the expression of lhr could
barely be detected in the immature ovary, but it became
detectable at the beginning of vitellogenesis and steadily
increased afterwards with the peak level reached at the
full-grown stage. At the follicle level, the expression
of fshr was very weak in the follicles of primary
growth
stage, but significantly increased with the follicles
entering vitellogenesis. However, after reaching the
maximal level in the mid-vitellogenic follicles, the level
of fshr expression dropped slightly but
significantly at
the full-grown stage. In comparison, the expression of
lhr obviously lagged behind that of fshr.
Its expression
became detectable only when the follicles started to
accumulate yolk granules, but the level rose steadily
afterwards and reached the peak at the full-grown stage
prior to oocyte maturation. These results suggest
differential roles for Fshr and Lhr in zebrafish ovarian
follicle development.
Key words:
Ovary
Follicle-stimulating hormone
Follicle-stimulating hormone receptor
Follicular development
Luteinizing hormone
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