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Molecular cloning and expression of interleukin-1 receptor-associated kinase 4, an important mediator of Toll-like receptor signal pathway, from small abalone Haliotis diversicolor

机译:小鲍鲍鱼嗜盐菌中白介素1受体相关激酶4(Toll样受体信号通路的重要介体)的分子克隆与表达

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Mammal interleukin-1 receptor-associated kinases (IRAKs) have been demonstrated to play important functions in TLRs (Toll-like receptor) signal pathway and T cell proliferation, but there is less knowledge available on mollusc IRAKs. In this study, a molluscan IRAK-4 gene, saIRAK-4, was cloned for the first time from the small abalone (Haliotis diversicolor). Its full-length cDNA sequence was 2062 bp, with a 1548 bp open reading frame encoding a protein of 516 aa. The molecular mass of the deduced protein was approximately 57.8 kDa with an estimated pI of 5.23, and showed highest identity (47%) to acorn worm Saccoglossus kowalevskii. Amino acid sequence analysis revealed saIRAK-4 shares conserved signature motifs with other IRAK-4 proteins, including the death domain (DD), serine/threonine/tyrosine protein kinase domain (STYKc), protein kinases ATP-binding region signature, serine/threonine protein kinases active-site signature and prokaryotic membrane lipoprotein lipid attachment site. Quantitative real-time PCR was employed to investigate the tissue distribution of saIRAK-4 mRNA, and its expression in abalone under bacteria challenge and larvae at different developmental stages. The 5aIRAK-4 mRNA could be detected in all examined tissues, with the highest expression level in gills, and was up-regulated in hemocytes and gills after bacteria injection. Additionally, 5aIRAK-4 was constitutively expressed at all examined developmental stages. These results indicate that saIRAK-4 could respond to pathogenic infection and may play an important role in the adult abalone immune system and early innate immunity in the process of abalone larval development
机译:哺乳动物白细胞介素1受体相关激酶(IRAKs)已被证明在TLRs(Toll样受体)信号通路和T细胞增殖中起着重要的作用,但是关于软体动物IRAKs的知识却很少。在这项研究中,软体动物IRAK-4基因saIRAK-4被首次从小鲍鱼(Haliotis diversicolor)中克隆出来。它的全长cDNA序列为2062 bp,带有1548 bp的开放阅读框,编码516 aa蛋白。推导的蛋白质的分子量约为57.8 kDa,估计pI为5.23,与橡果蠕虫Saccoglossus kowalevskii的同一性最高(47%)。氨基酸序列分析显示,saIRAK-4与其他IRAK-4蛋白具有保守的签名基序,包括死亡结构域(DD),丝氨酸/苏氨酸/酪氨酸蛋白激酶结构域(STYKc),蛋白激酶ATP结合区签名,丝氨酸/苏氨酸蛋白激酶活性位点签名和原核膜脂蛋白脂质附着位点。采用定量实时PCR研究saIRAK-4 mRNA的组织分布,以及在不同发育阶段细菌攻击和幼虫作用下其在鲍鱼中的表达。可以在所有检查的组织中检测到5aIRAK-4 mRNA,在g中表达水平最高,并且在细菌注射后在血细胞和g中上调。另外,在所有检查的发育阶段均组成性表达5aIRAK-4。这些结果表明,saIRAK-4可能对病原体感染有反应,并且可能在成年鲍鱼的免疫系统和鲍鱼幼体发育过程中的早期先天免疫中起重要作用。

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