首页> 外文期刊>Peptides: An International Journal >Molecular characterization, RNA interference and recombinant protein approach to study the function of the putative Molt Inhibiting Hormone (FmMIH1) gene from the shrimp Fenneropenaeus merguiensis
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Molecular characterization, RNA interference and recombinant protein approach to study the function of the putative Molt Inhibiting Hormone (FmMIH1) gene from the shrimp Fenneropenaeus merguiensis

机译:研究推定蜕皮抑制激素(FMMIH1)基因的功能,RNA干扰和重组蛋白质方法从虾Fenneropenaeus Merguiensis的函数

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The Molt Inhibiting Hormone gene and cDNA of the banana shrimp Fenneropenaeus merguiensis (FmMIH1) has been cloned and characterized. FmMIH1 possesses most of the characteristics of the eyestalk CHH/MIH/GIH family subtype-II neuropeptides. FmMIH1 open reading frame consists of 315 bp encoding for 105 amino acid residues. The mature peptide of FmMIH1 consists of 76 amino acid residues, a glycine residue at position 11 of the mature peptide and 6 cysteine residues located in the conserved position. In addition to eyestalk, high levels of FmMIH1 transcript could also be detected in the intestine. FmMIH1 transcript level is low throughout the post-molt, early to mid-intermolt and premolt. However, a sharp increase could be observed in late intermolt (C3 stage). Both alignment and phylogenetic analysis reveal that FmMIH1 is most similar to the MIH1 of other shrimps. For functional assay, RNA interference results show that a significant 2.3 days (P < 0.05) reduction in molt cycle duration could be observed in shrimp receiving dsFmMIH1 injection. Surprisingly, injection of recombinant FmMIH1 could also cause a significant reduction of the molt cycle (average 1.9 days, P < 0.05). We hypothesize that the recombinant protein is biological inactive but it competes with the endogenous MIH for carrier protein binding and consequently reduces the amount of biological MIH that could reach the targets. In conclusion, the result of this study will provide us new insight in molting/growth control in crustacean.
机译:克隆并表征了香蕉虾Fenneropenaeus(FmmiH1)的香蕉虾Fenneropeneaeus(FMMMIH1)的蜕皮抑制激素基因和cDNA。 FMMIH1拥有眼影CHH / MIH / GIH家族亚型-II神经肽的大部分特征。 FMMIH1开放阅读框架由315bp编码组成105个氨基酸残基。 FMMMIH1的成熟肽由76个氨基酸残基组成,在成熟肽的位置11处的甘氨酸残基和位于保守位置的6个半胱氨酸残基。除了眼展外,还可以在肠道中检测到高水平的FMMiH1转录物。在整个后蜕皮中,FMMiH1转录水平低,早期到中间电压和预压孔。然而,在后部电阻(C3阶段)中可以观察到急剧增加。对准和系统发育分析既表明,FMMIH1与其他虾的MIH1最相似。对于功能测定,RNA干扰结果表明,在虾接受DSFMMIH1注射中,可以观察到蜕皮循环持续时间的显着2.3天(P <0.05)。令人惊讶的是,注射重组FMMMMIH1也可能导致蜕皮循环的显着降低(平均1.9天,P <0.05)。我们假设重组蛋白是生物非活动的,但它与内源性MIH竞争载体蛋白结合,因此降低了可以到达靶标的生物miH的量。总之,本研究的结果将为我们提供甲壳类动物中蜕皮/生长控制的新见解。

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