林爱强, 谢仰杰, 徐双斌, 叶坤, 龚诗琦, 王志勇. 大黄鱼gsdfamh基因的克隆及表达分析[J]. 南方水产科学, 2017, 13(6): 1-13. DOI: 10.3969/j.issn.2095-0780.2017.06.001
引用本文: 林爱强, 谢仰杰, 徐双斌, 叶坤, 龚诗琦, 王志勇. 大黄鱼gsdfamh基因的克隆及表达分析[J]. 南方水产科学, 2017, 13(6): 1-13. DOI: 10.3969/j.issn.2095-0780.2017.06.001
LIN Aiqiang, XIE Yangjie, XU Shuangbin, YE Kun, GONG Shiqi, WANG Zhiyong. Cloning and expression profiling of gsdf and amh genes in large yellow croaker (Larimichthys crocea)[J]. South China Fisheries Science, 2017, 13(6): 1-13. DOI: 10.3969/j.issn.2095-0780.2017.06.001
Citation: LIN Aiqiang, XIE Yangjie, XU Shuangbin, YE Kun, GONG Shiqi, WANG Zhiyong. Cloning and expression profiling of gsdf and amh genes in large yellow croaker (Larimichthys crocea)[J]. South China Fisheries Science, 2017, 13(6): 1-13. DOI: 10.3969/j.issn.2095-0780.2017.06.001

大黄鱼gsdfamh基因的克隆及表达分析

Cloning and expression profiling of gsdf and amh genes in large yellow croaker (Larimichthys crocea)

  • 摘要: 该研究克隆了大黄鱼(Larimichthys croceagsdf (gonadal soma derived factor)和amh (anti-Müllerian hormone)基因的开放阅读框序列并对它们的表达进行分析。大黄鱼gsdf基因cDNA序列开放阅读框长为618 bp,可编码205个氨基酸,含有信号肽和TGF-β结构域。系统进化分析显示,大黄鱼Gsdf与其他鱼类Gsdf聚为一枝,而与TGF-β超家族其他成员分开。Amh基因cDNA序列开放阅读框为1 563 bp,可编码520个氨基酸,含有信号肽、AMH-N区域和TGF-β保守结构域。系统进化分析显示,大黄鱼Amh与舌齿鲈(Dicentrarchus labrax)Amh进化关系最近。荧光定量PCR表达分析显示,gsdfamh基因主要在大黄鱼性腺表达,在精巢中的表达量显著高于卵巢(P < 0.05),2个基因都在性腺分化前开始表达,在雄鱼精巢中表达量呈现先升高后下降的趋势,在卵巢的表达量很低。此外,相比于正常雌鱼,gsdfamh基因在伪雄鱼(遗传性雌鱼)性腺中的表达量显著上调。这些结果表明,gsdfamh基因在大黄鱼性腺分化过程中起到重要的作用。

     

    Abstract: In this study, the gonadal soma derived factor (gsdf) and anti-Müllerian hormone (amh) were cloned from Larimichthys crocea, and their expression patterns were analysed by qRT-PCR. The results shows that the open reading frame (ORF) of gsdf gene spaned a region of 618 bp and coded 205 amino acids with a signal peptide and a conserved domain of the TGF-β superfamily. Sequence alignment analysis reveals that the gsdf of L.crocea and Dicentrarchus labrax shared the highest homology. Phylogenetic analysis shows that the fish Gsdf proteins had a clade separated from the rest members of the TGF-β superfamily. The ORF of amh gene spaned a region of 1 563 bp and coded 520 amino acids that contained a signal peptide, an AMH-N domain and a TGF-β conserved domain. Phylogenetic analysis shows that Amh proteins of L.crocea and D.labrax had the nearest relationship. The qPCR analysis reveals that gsdf and amh genes were expressed mainly in gonad, and the expression levels in testis were significantly higher than that in ovary (P < 0.05). Before the gonad differentiation, gsdf and amh genes had already expressed, and the expression levels of two genes showed an increase-decrease trend in testis whereas the expression levels were very low in ovaries. Besides, compared with normal females, the expressions of two genes had more significant expression in gonad of pseudo-males (genetic females). It is indicated that gsdf and amh genes play a very important role in the process of L.crocea gonad differentiation.

     

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