首页> 外文期刊>Journal of the World Aquaculture Society >Molecular Cloning, Characterization, and Expression of Two Myeloid Differentiation Factor 88 (Myd88) in Pacific Oyster, Crassostrea gigas
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Molecular Cloning, Characterization, and Expression of Two Myeloid Differentiation Factor 88 (Myd88) in Pacific Oyster, Crassostrea gigas

机译:太平洋牡蛎(Crassostrea gigas)中两个髓样分化因子88(Myd88)的分子克隆,表征和表达

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Myeloid differentiation factor 88 (MyD88) is a universal adaptor protein and plays an important role in the signal transduction of Toll/interleukin-1 receptor (TIR/IL-1R) family. In this study, two novel molluskan MyD88 family members (named as CgMyD88-1 and CgMyD88-2) were identified from the Pacific oyster, Crassostrea gigas. The full-length cDNA of CgMyD88-1 was of 2453 base pairs (bp), with an open reading frame (ORF) of 1077bp encoding 358 amino acids. The cDNA of CgMyD88-2 consists of 1374bp ORF encoding 457 amino acids. Both CgMyD88s contain death domain (DD) and TIR domain which are typical features of MyD88 family proteins. Three conserved boxes were also found in the two CgMyD88s which were similar to MyD88s in vertebrates. The expression level of both CgMyD88 mRNAs in selected tissues was measured by quantitative real-time polymerase chain reaction (qRT-PCR). Both CgMyD88 transcripts were constitutively expressed in all tested tissues. Gill and hemocytes were shown with highest expression levels while adductor muscle and gonad were with lower levels. The CgMyD88 transcripts in hemocytes after ostreid herpesvirus 1 (OsHV-1) challenge were also determined by qRT-PCR. Both CgMyD88s were significantly upregulated in hemocytes after OsHV-1 challenge and had significant differences (P < 0.05) at some time points compared with the control. Our results as previously reported suggest that MyD88-dependent pathway exists in C. gigas, and its critical adaptor CgMyD88 plays important roles in oysters' innate immune defense against OsHV-1 infection.
机译:髓样分化因子88(MyD88)是一种通用的衔接蛋白,在Toll / IL-1受体(TIR / IL-1R)家族的信号转导中起重要作用。在这项研究中,从太平洋牡蛎Crassostrea gigas中鉴定了两个新的软体动物MyD88家族成员(分别命名为CgMyD88-1和CgMyD88-2)。 CgMyD88-1的全长cDNA为2453个碱基对(bp),带有1077bp的开放阅读框(ORF),编码358个氨基酸。 CgMyD88-2的cDNA由1374bp ORF组成,编码457个氨基酸。这两个CgMyD88都包含死亡域(DD)和TIR域,这是MyD88家族蛋白的典型特征。在两个CgMyD88中还发现了三个保守框,它们与脊椎动物中的MyD88相似。通过定量实时聚合酶链反应(qRT-PCR)测量所选组织中两个CgMyD88 mRNA的表达水平。两种CgMyD88转录本均在所有测试组织中组成性表达。 ill和血细胞的表达水平最高,而内收肌和性腺的表达水平较低。还通过qRT-PCR确定了ostreid疱疹病毒1(OsHV-1)攻击后血细胞中的CgMyD88转录本。与对照组相比,OsHV-1攻击后,两个CgMyD88s在血细胞中均显着上调,并且在某些时间点上具有显着差异(P <0.05)。如先前报道的我们的结果表明,MyD88依赖性途径存在于C. gigas中,其关键衔接子CgMyD88在牡蛎对OsHV-1感染的先天免疫防御中起重要作用。

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