University of Bari Aldo Moro, Department of Animal Production, Valenzano, Italy.
Anim Reprod Sci. 2012 May;132(1-2):101-10. doi: 10.1016/j.anireprosci.2012.03.014. Epub 2012 Apr 4.
The cDNA sequences of vitellogenin receptor proteins (VgR(+) and VgR(-)), containing or lacking the O-linked sugar domain, were determined in Atlantic bluefin tuna (Thunnus thynnus L.). VgR(-) gene expression in the ovary was compared in captive-reared and wild Atlantic bluefin tuna during the reproductive cycle. Gonad samples from adult fish were sampled from 2008 to 2010 from stocks reared in captivity at different commercial fattening operations in the Mediterranean Sea and from wild individuals caught either by traditional tuna traps during their migration towards the spawning grounds in the Mediterranean Sea or by the long-line artisanal fishery. In addition, juvenile male and female Atlantic bluefin tuna were sampled from a farming facility, to obtain baseline information and pre-adulthood amounts of VgR(-). The total length of VgR(+) cDNA was 4006 nucleotides (nt) and that of VgR(-) was 3946 nt. Relative amounts of VgR(-) were greater in juvenile females and in those adults having only previtellogenic oocytes (119 ± 55 and 146 ± 26 folds more than juvenile males, respectively). Amounts of VgR(-) were less in individuals with yolked oocytes (ripening stage, May-June) and increased after spawning in July (92 ± 20 and 113 ± 13 folds more than juvenile males in ripening and post-spawning fish, respectively). These data suggest that regulation of VgR(-) is not under oestrogen control. During the ripening period, greater VgR(-) gene expression was observed in wild fish than in fish reared in captivity, possibly because of (a) differences in water temperature exposure and/or energy storage, and/or (b) an inadequate diet in reared Atlantic bluefin tuna.
已确定含有或不含有 O-连接糖域的卵黄蛋白原受体蛋白 (VgR(+) 和 VgR(-)) 的 cDNA 序列,在大西洋金枪鱼 (Thunnus thynnus L.) 中。在生殖周期中,比较了大西洋金枪鱼养殖和野生群体卵巢中 VgR(-) 基因的表达。从 2008 年到 2010 年,从在地中海不同商业育肥作业中养殖的成年鱼类的性腺样本,以及从通过传统金枪鱼陷阱在其向地中海产卵场洄游期间捕获的野生个体中采集性腺样本,或者通过延绳钓渔业。此外,从养殖设施中采集了幼大西洋金枪鱼的雌雄样本,以获得基线信息和成年前 VgR(-) 的数量。VgR(+) cDNA 的全长为 4006 个核苷酸 (nt),VgR(-) 的全长为 3946 nt。VgR(-) 的相对数量在幼雌鱼和仅具有前卵黄生成卵母细胞的成年鱼中更高(分别比幼雄鱼高 119 ± 55 和 146 ± 26 倍)。在具有卵黄卵母细胞的个体中(成熟阶段,5 月至 6 月)数量较少,并且在 7 月产卵后增加(在成熟和产卵后鱼中分别比幼雄鱼高 92 ± 20 和 113 ± 13 倍)。这些数据表明,VgR(-) 的调节不受雌激素控制。在成熟期间,野生鱼中观察到的 VgR(-) 基因表达高于养殖鱼,可能是由于 (a) 暴露于不同的水温以及/或能量储存,和/或 (b) 养殖大西洋金枪鱼的饮食不足。