稀有鮈鲫MHCβ基因克隆及鲁氏耶尔森菌感染后的表达分析

Cloning of the MHCβ gene in Gobiocypris rarus and expression analysis after Yersinia ruckeri infection

  • 摘要: 为探究稀有鮈鲫MHCβ基因的分子特征及其表达特点,采用PCR扩增技术获得了稀有鮈鲫MHCβ cDNA序列810 bp,包括开放阅读框 (ORF)759 bp,编码252个氨基酸。生物信息分析表明,MHC Ⅱβ氨基酸序列存在4个保守的半胱氨酸残基和GXXGXXXGXXXXXXG结构,与其他亲缘鱼类的一致性为51.78%~80.56%,其编码的蛋白质分子包括1个信号肽、1个MHC Ⅱβ (β-1)结构域、1个IGc1 (β-2)结构域和1个跨膜螺旋区域。实时荧光定量PCR (qRT-PCR)结果显示,MHCβ在脾脏表达量最高,头肾、鳃、皮肤表达量较高。人工感染鲁氏耶尔森菌后,6 h时在头肾表达呈显著上调,肝脏中在12 h开始出现极显著上调,皮肤中在24 h和48 h表达极显著,鳃中在6~24 h表达极显著,脾脏中则是在6 h出现极显著下调,于96 h接近对照组表达水平。初步研究表明,MHCβ在鱼类抵御细菌感染的免疫反应中发挥着重要作用,为进一步揭示稀有鮈鲫MHC家族的功能提供了参考依据。

     

    Abstract: In order to explore the molecular characteristics and expression characteristics of the rare minnow MHCβ gene, the 810 bp cDNA sequence of the rare minnow Gobiocypris rarus MHCβ was obtained by PCR amplification technology, including an open reading frame (ORF) of 759 bp, encoding 252 amino acids (aa). Bioinformatics analysis showed that there were four conserved cysteine residues and a GXXGXXXGXXXXXXG structure in the amino acid sequence of MHC IIβ, and the consistency with other relative fish was 51.78%-80.56%. The encoded protein molecules included a signal peptide, a MHC IIβ (β-1) domain, a IGc1 (β-2) domain and a transmembrane helical region. Quantitative Real-time PCR (qRT-PCR) results showed that the expression of MHCβ gene was the highest in spleen, and higher in head kidney, gill and skin. After artificial infection with pathogenic bacteria, Yersinia ruckeri, the expression of head kidney was significantly up-regulated at 6 h, and liver was significantly up-regulated at 12 h, skin was significantly up-regulated at 24 h and 48 h, gill was significantly up-regulated at 6 to 24 h, and spleen was significantly down-regulated at 6 h, and approached the expression level of the control group at 96 h. The results show that MHC IIβ plays an important role in immune response, which provides reference for further revealing the regulatory mechanism of MHC family immune defense.

     

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