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Total follicular populations and peripheral plasma concentrations of LH, FSH, prolactin, oestradiol-17 beta and progesterone during the preceding cycle were studied in two breeds of sheep (Romanov and Ile-de-France) which differed widely in their ovulation rates (3.2 and 1.5 respectively). No LH parameters could be correlated with the follicular details measured. The second peak of FSH occurring 20-30 h after the preovulatory surge of LH was significantly larger in the Romanov ewes and the area under this peak was correlated (P less than 0.01) with the number of antral follicles present in the ovary 17 days later. This suggests that formation of the antrum during the follicular growth phase is under the control of FSH. The discharge of prolactin preceding the LH peak, although not significantly different between breeds, was correlated with several of the follicular classes measured, including the number of preantral follicles. The peak value of oestradiol-17 beta measured before the LH peak was significantly higher (P less than 0.05) in the Romanov ewes and was correlated with the number of the largest follicles present. There was no significant difference between breeds in the concentration of oestradiol at the onset of oestrus. The progesterone concentration during the luteal phase was highly correlated with the number of preovulatory follicles.

We report the complementary DNA structure obtained by reverse transcription and polymerase chain reaction amplification encoding the complete amino acid sequence for the bovine follicle-stimulating hormone receptor (bFSHr). The deduced amino acid sequence for the cDNA revealed a mature polypeptide consisting of 678 amino acids (theoretical weight of 76.4 kDa) and a 17 amino acid putative leading signal peptide. The receptor consists of a large NH2-terminal extracellular membrane domain of 349 aa with 3 potential N-linked glycosylation sites, a transmembrane domain (264 aa) consisting of 7 putative membrane spanning segments, and an intracytoplasmic COOH-terminal domain (65 aa). Four potential phosphorylation sites were found in the transmembrane domain and the COOH-terminal domain. The amino acid sequence is 97%, 89%, and 88% homologous to the ovine, human, and rat FSHr respectively, with complete conservation of the 22 cysteine residues in the whole protein and the 3 N-linked glycosylation sites on the extracellular membrane domain. Northern blot analysis of total mRNA in bovine tissues revealed a major mRNA transcript of 2.55 kb for the bFSHr in the ovary without corpus luteum, and in the testis. No expression was found in other tissues analyzed. Total RNA from bovine granulosa cells collected from pregnant mare serum gonadotropin (PMSG)-treated prepubertal heifers showed 2 major mRNA transcripts of 6.8 and 2.55 kb, and 3 minor transcripts of 3.8, 3.3, and 1.6 kb. Bovine granulosa cells cultured with porcine FSH (0, 2, 10 ng/ml) for 4 days showed a decrease in the steady state level of the FSHr mRNA.(ABSTRACT TRUNCATED AT 250 WORDS)