首页> 外文期刊>International journal of biological sciences >C1q-like Factor, a Target of miR-430, Regulates Primordial Germ Cell Development in Early Embryos of Carassius auratus
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C1q-like Factor, a Target of miR-430, Regulates Primordial Germ Cell Development in Early Embryos of Carassius auratus

机译:C1Q样因子,miR-430的目标,调节鲫鱼早期胚胎的原始胚芽细胞发育

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C1q-like is a significant maternal factor of TNF/C1q super-family, and the abundant protein has been observed in both mature eggs of Carassius auratus and Carassius auratus gibelio, but its biological function in early embryo development has remained unclear. In this study, we firstly revealed a high level of maternal C1q-like transcript existence only in mature eggs of Carassius auratus, whereas no any maternal C1q-like transcript was observed in that of Carassius auratus gibelio. During embryonic development, the C1q-like zygotic expression begins around cardiopalmus stage in embryos of both Carassius auratus and Carassius auratus gibelio. Then, we examined the biological role of C1q-like by morpholino-mediated knockdown in early embryo development. Knockdown of CaOC1q resulted in a significant reduction of primordial germ cells (PGCs) in Carassius auratus, as shown by whole mount in situ hybridization with vasa-specific RNA probe, fluorescence immunostaining of vasa protein, and GFP imaging of the GFP-nanos1-3'UTR mRNA reporter. In vitro and in vivo evidence indicated that a microRNA, miR-430 could repress the C1q-like expression and PGC development. These data suggest that C1q-like should be a direct target of miR-430 and play an essential role in PGC development of Carassius auratus.
机译:C1Q样是TNF / C1Q超级家庭的重要母体因子,并且在Carassius Auratus和Carassius Auratus Gibelio的成熟卵中观察到丰富的蛋白质,但其早期胚胎发育的生物学功能仍不清楚。在这项研究中,我们首先揭示了一种高水平的母体C1Q样本的成绩在Carassius auratus的成熟卵中,而没有在Carassius Auratus Gibelio中观察到任何母体C1Q样转录物。在胚胎发育期间,C1Q样的Zygotic表达在Carassius Auratus和Carassius auratus Gibelio的胚胎中致脉络膜阶段。然后,我们在早期胚胎发育中调查了C1Q样变质的敲低的生物学作用。 CAOC1Q的敲低导致Carassius Auratus的原始生殖细胞(PGC)显着减少,如全坐原位杂交,与VASA蛋白的荧光免疫染色和GFP-NANOS1-3的GFP成像所示'UTR mRNA记者。体外和体内证据表明,MICRRNA,MIR-430可以抑制C1Q样表达和PGC发育。这些数据表明C1Q样应该是MIR-430的直接目标,并在Carassius Auratus的PGC开发中发挥重要作用。

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