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Molecular Characterization and Functional Study of Insulin-Like Androgenic Gland Hormone Gene in the Red Swamp Crayfish, Procambarus clarkii

机译:红沼泽小龙虾,Procambarus clarkii中胰岛素样雄激素腺激素基因的分子表征及功能研究

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摘要

The androgenic gland (AG) is a male-specific endocrine organ that controls the primary and secondary sexual characteristics in male crustaceans. More evidence indicates that the insulin-like androgenic gland hormone gene (IAG) is the key male sexual differentiation factor, particularly the application of RNA interference (RNAi) technology on IAG. In this study, the full-length cDNA of IAG (termed PcIAG) was isolated from the red swamp crayfish, Procambarus clarkii. Tissue distribution analysis showed that in addition to its expression in the AG of male P. clarkii, PcIAG was widely expressed in female tissues and other male tissues. The PcIAG protein was detected in the reproductive and nervous systems of adult male P. clarkii. Additionally, RNAi results showed that the PcIAG expression could be silenced efficiently, and the male sperm maturation and release possibly present a transient adverse interference at lower doses (0.1 μg/g and 1 μg/g) of PcIAG−dsRNA (PcIAG double-stranded RNA). Dramatically, the expression level of PcIAG increased sharply shortly after the injection of higher doses (5 μg/g and 10 μg/g) of PcIAG−dsRNA, which might accelerate the maturation and release of sperm. Moreover, the expression of PcSxl (P. clarkii Sex-lethal) was detected by Quantitative Real-Time PCR (qPCR) after the injection of PcIAG−dsRNA to explore whether the PcIAG gene regulates the PcSxl gene, and we found that the PcIAG did not directly regulate PcSxl in P. clarkii. The study could help accelerate the progress of PcIAG functional research and provide a useful reference for the single-sex selective breeding of P. clarkii.
机译:雄激素(Ag)是一种雄性特异性内分泌器官,用于控制雄性甲壳类动物中的初级和继发性特征。更多证据表明胰岛素样雄激素腺激素基因(IAG)是关键的男性性分化因子,特别是RNA干扰(RNAi)技术在IAG上的应用。在这项研究中,IAG(称为PCIAG)的全长cDNA与红沼泽小龙虾,Procambarus clarkii分离。组织分布分析表明,除了在男性P.Clarkii的AG中表达,PCIAG在女组织和其他雄性组织中被广泛表达。在成年男性P.Clarkii的生殖和神经系统中检测到PCIAG蛋白。另外,RNAI结果表明,PCIAG表达可以有效地沉默,并且雄性精子成熟和释放可能在低剂量(0.1μg/ g和1μg/ g)的PCIAG-dsRNA(PCIAG双链时呈现瞬时不利干扰RNA)。显着地,在注射较高剂量(5μg/ g和10μg/ g)的PCIAG-DSRNA后,PCIAG的表达水平急剧增加,这可能会加速精子的成熟和释放。此外,通过定量实时PCR(QPCR)在注射PCIAG-DSRNA后检测PCSX1(P.Crarkii性别致死)的表达,以探索PCIAG基因是否调节PCSXL基因,我们发现PCIAG确实如此不直接调节P. Clarkii中的PCSXL。该研究可以帮助加速PCIAG功能研究的进展,并为P.Clarkii的单性选择性育种提供了有用的参考。

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