Matsumoto Toshie, Yamano Keisuke, Kitamura Makiko, Hara Akihiko
National Research Institute of Aquaculture, Minami-ise, Mie 516-0193 Japan.
Comp Biochem Physiol A Mol Integr Physiol. 2008 Mar;149(3):293-8. doi: 10.1016/j.cbpa.2008.01.003. Epub 2008 Jan 11.
Only a few biochemical and molecular studies on yolk proteins (vitellins) have been carried out in mollusks, mainly in bivalves, while information on prosobranch vitellogenesis is still limited. In this study, we cloned a full-length cDNA encoding vitellogenin (Vg) in the Pacific abalone Haliotis discus hannai. The complete Vg cDNA consists of 7753 nucleotides with a long open reading frame encoding 2391 amino acid residues. The deduced primary structure contains the N-terminal amino acid sequences of the 95 kDa and 150 kDa subunits of vitellin of the abalone and shows similarities to Vgs of other mollusk, fish, nematode and coral species. In common with bivalve Vgs, the abalone Vg gene was expressed only in the ovary. In situ hybridization analysis further localized Vg mRNA to the follicle cells in the ovary. We conclude that the follicle cells are the site of Vg synthesis in H. discus hannai.
在软体动物中,尤其是双壳贝类中,仅开展了少量关于卵黄蛋白(卵黄磷蛋白)的生化和分子研究,而关于前鳃亚纲动物卵黄发生的信息仍然有限。在本研究中,我们克隆了皱纹盘鲍(Haliotis discus hannai)中编码卵黄蛋白原(Vg)的全长cDNA。完整的Vg cDNA由7753个核苷酸组成,具有一个长开放阅读框,编码2391个氨基酸残基。推导的一级结构包含鲍鱼卵黄磷蛋白95 kDa和150 kDa亚基的N端氨基酸序列,并且与其他软体动物、鱼类、线虫和珊瑚物种的Vg具有相似性。与双壳贝类Vg一样,鲍鱼Vg基因仅在卵巢中表达。原位杂交分析进一步将Vg mRNA定位到卵巢中的卵泡细胞。我们得出结论,卵泡细胞是皱纹盘鲍中Vg合成的部位。