Gonadotropin regulation of genes differentially expressed in response to PKCzeta inhibitor during ovulation in the rat.

AIMS:The aim of the present study was to characterize genes regulated by protein kinase C inhibitor in the preovulatory granulosa cells following LH stimulation in the rat ovary. MAIN METHODS:Annealing control primer (ACP)-based polymerase chain reaction (PCR) method was used to identify differentially expressed genes in granulosa cells of preovulatory follicles cultured in the presence of luteinizing hormone (LH) and myristoylated duanyu1531zeta pseudosubstrate peptide or a similarly sized control peptide. KEY FINDINGS:Among the 16 genes identified, five (testin, glypican-4, retrovirus SC1, aminolevulinic acid synthase 1 and serum-inducible kinase) experienced rapid and transient stimulation of gene expression upon exposure to human chorionic gonadotropin (hCG) in the ovary of immature rats primed with pregnant mare's serum gonadotropin (PMSG). In situ hybridization analysis revealed that hCG administration induced expression of these five genes in granulosa cells of preovulatory follicles. The Western analysis showed that the protein levels of testin and serum-inducible kinase were also increased by hCG. Expression of the eleven remaining genes in the ovary remained high at 24-72 h following hCG treatment. SIGNIFICANCE:The present data demonstrate the gonadotropin stimulation of genes differentially expressed by duanyu1531zeta inhibitor, implicating that duanyu1531zeta pathway possibly plays a role in controlling the ovulation process.

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