In this study, we cloned a full-length cDNA encoding vitellogenin (Vg) in the Fujian oyster Crassostrea angulata. The complete Vg cDNA consists of 5160 nucleotides with a long open reading frame encoding 1641 amino acid residues. The deduced amino acid sequence shared high similarity with the Vgs of other mollusc, fish, nematode and arthropod species, particularly in the N-terminal region. We analyzed the spatiotemporal expression of caVg transcripts by Real-time Quantitative PCR. In common with other mollusc Vgs, the caVg gene was expressed primarily in the ovary, and the levels were 348 and 177 times higher in maturation and ripeness stages (P<0.01), respectively, than in the partially spent stage. There was negligible expression in male oysters. In situ hybridization analysis further localized caVg mRNA to the follicle cells (also named auxiliary cells) surrounding the oocytes in the ovary. Moreover, in vivo waterborne exposure experiments in early gametogenesis oysters showed that estradiol-17β (E2) administration resulted in a significant increase in caVg mRNA expression. We conclude that caVg is synthesized in the follicle cell surrounding the vitellogenic oocyte in C. angulata, and directly passed to oocytes through the extracellular space without mediation through hemolymph. Also, we hypothesize that this process is mediated by E2 in a dose dependent.
Keywords: Crassostrea angulata; Estradiol-17β; Follicle cell; Oyster; Vitellogenin gene.
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