Shikina Shinya, Chiu Yi-Ling, Lee Yan-Horn, Chang Ching-Fong
Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung, Taiwan Institute of Marine Environment and Ecology, National Taiwan Ocean University, Keelung, Taiwan
Department of Aquaculture, National Taiwan Ocean University, Keelung, Taiwan.
Biol Reprod. 2015 Sep;93(3):57. doi: 10.1095/biolreprod.115.129643. Epub 2015 Jul 15.
To gain a better understanding of how corals form their eggs at both the molecular and cellular levels, we performed a differential screen (suppression subtractive hybridization) to identify genes related to oocyte development in a stony coral, Euphyllia ancora. Through the course of screening, a novel gene that contains three alternate repeats of fibronectin domain 2 and epidermal growth factor (EGF)-like domains, as well as an additional calcium-binding EGF-like domain (EGF-CA), was identified and tentatively named euphy after the scientific name of the coral, E. ancora. Quantitative RT-PCR revealed that expression levels of euphy increased in female colonies as the coral approached reproductive season. Tissue distribution analysis followed by mRNA in situ hybridization revealed that euphy is highly expressed in the ovarian (mesenterial) somatic cells in the body of E. ancora. Staining of tissue sections with an antibody against euphy protein (Euphy) revealed Euphy immunoreactivity in both ovarian somatic cells and oocytes. Subsequent Western blotting demonstrated the presence of abundant Euphy in unfertilized mature eggs. These results indicate that Euphy produced in the ovarian somatic cells is transported to and accumulates within oocytes as a yolk protein during oogenesis. We previously showed that two major yolk proteins, vitellogenin and egg protein, are similarly produced by ovarian somatic cells. Hence, the present study uncovered the third ovarian somatic-derived yolk protein in corals. Our data provide new information that contributes to a more comprehensive understanding of coral egg formation.
为了在分子和细胞水平上更好地了解珊瑚如何形成卵子,我们进行了差异筛选(抑制性消减杂交),以鉴定与石珊瑚鹿角杯形珊瑚(Euphyllia ancora)卵母细胞发育相关的基因。在筛选过程中,我们鉴定出一个新基因,该基因包含纤连蛋白结构域2和表皮生长因子(EGF)样结构域的三个交替重复序列,以及一个额外的钙结合EGF样结构域(EGF-CA),并根据珊瑚的学名E. ancora,将其暂命名为euphy。定量逆转录聚合酶链反应(RT-PCR)显示,随着珊瑚接近繁殖季节,雌性群体中euphy的表达水平升高。随后通过mRNA原位杂交进行的组织分布分析表明,euphy在鹿角杯形珊瑚体内的卵巢(肠系膜)体细胞中高度表达。用抗euphy蛋白(Euphy)的抗体对组织切片进行染色,结果显示卵巢体细胞和卵母细胞中均有Euphy免疫反应性。随后的蛋白质免疫印迹法表明,未受精的成熟卵子中存在大量的Euphy。这些结果表明,在卵子发生过程中,卵巢体细胞产生的Euphy作为一种卵黄蛋白被转运到卵母细胞并在其中积累。我们之前表明,两种主要的卵黄蛋白,即卵黄生成素和卵蛋白,同样是由卵巢体细胞产生的。因此,本研究发现了珊瑚中第三种源自卵巢体细胞的卵黄蛋白。我们的数据提供了新的信息,有助于更全面地了解珊瑚卵子的形成。