首页> 外文期刊>Fish & Shellfish Immunology >Characterization of LPS-induced TNF alpha factor (LITAF) from orange-spotted grouper, Epinephelus coioides.
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Characterization of LPS-induced TNF alpha factor (LITAF) from orange-spotted grouper, Epinephelus coioides.

机译:LPS诱导的橙色斑点石斑鱼石斑鱼石斑鱼的TNFα因子(LITAF)的表征。

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摘要

Lipopolysaccharide-induced TNF alpha factor (LITAF) is an important transcription factor that mediates cell apoptosis and inflammatory response. In the present study, we cloned and characterized a LITAF gene from orange-spotted grouper (Epinephelus coioides) (Ec-LITAF). Ec-LITAF encoded a predicted 142 amino acid protein which shared 74% identity to sablefish (Anoplopoma fimbria) LITAF homolog. Multiple amino acid alignment showed that Ec-LITAF contained a typical LITAF domain with two CXXC motifs. Phylogenetic analysis indicated that Ec-LITAF was closely related to that of sablefish. Ec-LITAF mRNA was widely expressed in different tissues and its expression level in spleen was up-regulated after Singapore grouper iridovirus (SGIV) infection. Subcellular localization analysis revealed that the distribution of Ec-LITAF showed diffuse and aggregated patterns in cytoplasm. Interestingly, the distribution of Ec-LITAF overlayed with a viral LITAF homolog (vLITAF) encoded by SGIV. Overexpression of Ec-LITAF in vitro up-regulated the expression of tumor necrosis factors (TNF1 and TNF2) and TNF receptors (TNFR1 and TNFR2), and the expression of itself initiated apoptosis in fish cells. In addition, overexpression of Ec-LITAF not only accelerated SGIV infection induced CPE and cell death, but also increased viral gene transcription. Taken together, our data suggested that Ec-LITAF might play crucial roles during SGIV replication.
机译:脂多糖诱导的TNFα因子(LITAF)是介导细胞凋亡和炎症反应的重要转录因子。在本研究中,我们从桔斑石斑鱼(Epinephelus coioides)(Ec-LITAF)克隆并鉴定了LITAF基因。 Ec-LITAF编码一种预测的142个氨基酸蛋白质,与黑(Anoplopoma fimbria)LITAF同源物具有74%的同一性。多个氨基酸比对表明,Ec-LITAF包含具有两个CXXC图案的典型LITAF域。系统发育分析表明,Ec-LITAF与黑able密切相关。 Ec-LITAF mRNA在新加坡石斑鱼虹膜病毒(SGIV)感染后在不同组织中广泛表达,其在脾脏中的表达水平上调。亚细胞定位分析表明,Ec-LITAF的分布在细胞质中表现出弥散和聚集的模式。有趣的是,Ec-LITAF的分布覆盖了由SGIV编码的病毒LITAF同源物(vLITAF)。体外Ec-LITAF的过表达上调了肿瘤坏死因子(TNF1和TNF2)和TNF受体(TNFR1和TNFR2)的表达,而其自身的表达则引发了鱼细胞的凋亡。此外,Ec-LITAF的过表达不仅加速了SGIV感染诱导CPE和细胞死亡,而且还增加了病毒基因的转录。综上所述,我们的数据表明Ec-LITAF可能在SGIV复制过程中发挥关键作用。

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