亚洲鲈鱼抗RGNNV宿主免疫应答中两个ISG15同源物的鉴定

R.S. Krishna Priya , Avinash Premraj , K.C. Sivakumar , T.P. Sajeevan
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引用次数: 6

摘要

干扰素刺激基因(ISG)15是一种被病毒感染诱导的泛素样蛋白。本研究报道了在亚洲海鲈中鉴定出两个ISG15同源物LcISG15A和LcISG15B。克隆的LcISG15A cDNA片段含有一个474 bp的ORF,编码一个157个氨基酸的蛋白,而LcISG15B则含有一个498 bp的ORF,编码一个165个氨基酸的稍长蛋白。这两个蛋白都具有两个串联泛素样结构域和ISG15的c端LRGG基序特征。LcISG15B蛋白在LRGG基序之后有一个10个氨基酸的c端延伸。分子对接研究表明,LcISG15A比LcISG15B在泛素结构域和催化功能上表现出更多的构象变异性。Lates的ISG15A和ISG15B基因位于基因组中,具有两个外显子和一个内含子的基本结构,但只有第二个外显子编码蛋白质。这些基因还在启动子区域具有ifn刺激反应元件(ISRE),在3 ' UTR区域具有atta不稳定性基序。在头部、肾脏、心脏、脾脏和鳃等富含白细胞的器官中,ISG15A和ISG15B的基础表达水平较高。Poly (I:C)注射可迅速上调这些组织中ISG15基因的转录。红斑石斑鱼神经坏死病毒体内感染也可诱导头肾、脾、心和鳃中ISG15基因的上调。这些发现表明,这两个ISG15同源物可能在先天性抗病毒免疫中发挥重要作用,可用于改进预防策略和开发物种特异性免疫工具。
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Identification of two ISG15 homologues involved in host immune response against RGNNV in Asian seabass (Lates calcarifer)

Interferon Stimulated Gene (ISG)15 is a ubiquitin-like protein that is induced upon viral infections. Our study reports the identification of two homologues of ISG15 in the Asian seabass designated LcISG15A and LcISG15B. The cloned LcISG15A cDNA fragment contained a 474 bp ORF encoding a 157 amino acid protein whereas LcISG15B featured a 498 bp ORF encoding a slightly longer protein of 165 amino acids. Both proteins featured the two tandem ubiquitin-like domains and the C-terminal LRGG motif characteristic of ISG15. The LcISG15B protein has a 10-amino acid C-terminal extension after the LRGG motif. Molecular docking studies revealed that LcISG15A showed more conformational variability of the ubiquitin domains and catalytic function than LcISG15B. The Lates ISG15A and ISG15B genes, reside close in the genome, share the same basic structure with two exons and an intron, but only the second exon encoding the protein. These genes also featured the IFN-stimulatory response elements (ISRE) in the promoter region and ATTTA instability motif in the 3′ UTR region. Leukocyte-rich organs such as the head kidney, heart, spleen, and gill showed higher levels of ISG15A and ISG15B basal expression. Poly (I:C) injection rapidly upregulated the transcription of both the ISG15 genes in these tissues in Lates. In-vivo viral infection by red-spotted grouper nervous necrosis virus also induced upregulation of ISG15 genes in the head kidney, spleen, heart and gill. These findings indicate that the two ISG15 homologues may play a crucial role in innate antiviral immunity and could be used to improve prophylactic strategies and develop species-specific immunological tools for Lates calcarifer.

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