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首页> 外文期刊>Genetics and Molecular Research >Cloning, characterization, and expression of the macrophage migration inhibitory factor gene from the Pacific white shrimp Litopenaeus vannamei (Penaeidae)
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Cloning, characterization, and expression of the macrophage migration inhibitory factor gene from the Pacific white shrimp Litopenaeus vannamei (Penaeidae)

机译:太平洋白虾凡纳滨对虾(Penaeidae)巨噬细胞迁移抑制因子基因的克隆,鉴定和表达

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The macrophage migration inhibitory factor (MIF) is an important proinflammatory cytokine that mediates both innate and adaptive immune responses. In this study, we identified a homolog of MIF in the Pacific white shrimp Litopenaeus vannamei. The MIF cDNA contained a 363-bp open reading frame encoding a 120-amino acid protein with a calculated molecular mass of 13.442 kDa and a theoretical isoelectric point of 6.57. The L. vannamei MIF shared high amino acid identity with MIFs of other invertebrates. Tissue distribution analysis by quantitative real-time polymerase chain reaction (qRT-PCR) revealed that the L. vannamei MIF was abundantly expressed in the blood, heart, and hepatopancreas, was moderately expressed in the gill, and was weakly expressed in the muscle and intestine. Furthermore, in order to gain a basic understanding of the role of MIF in the shrimp immune response against viral infection, its mRNA expression was determined in the hepatopancreas of L. vannamei at different stages after white spot syndrome virus (WSSV) challenge using qRT-PCR. The result indicated that the expression of MIF was significantly upregulated after WSSV injection, suggesting that MIF may be involved in the response to viral infection in shrimp.
机译:巨噬细胞迁移抑制因子(MIF)是重要的促炎细胞因子,可介导先天和适应性免疫应答。在这项研究中,我们确定了太平洋白虾凡纳滨对虾中的MIF同源物。 MIF cDNA包含一个363-bp的开放阅读框,编码120个氨基酸的蛋白质,计算的分子量为13.442 kDa,理论等电点为6.57。南美白对虾的MIF与其他​​无脊椎动物的MIF具有高度的氨基酸同一性。通过定量实时聚合酶链反应(qRT-PCR)进行的组织分布分析显示,南美白对虾MIF在血液,心脏和肝胰腺中大量表达,在腮中中等表达,在肌肉和皮肤中较弱表达。肠。此外,为了基本了解MIF在虾对病毒感染的免疫应答中的作用,使用qRT-PCR技术在白斑综合症病毒(WSSV)攻击后的不同阶段测定了南美白对虾肝胰腺中的MIF表达。 PCR。结果表明,WSSV注射后,MIF的表达明显上调,表明MIF可能参与了虾对病毒感染的反应。

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