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鸭核转运蛋白α4(duKPNA4)参与I型干扰素的表达以及针对日本脑炎病毒的抗病毒反应。

Duck karyopherin α4 (duKPNA4) is involved in type I interferon expression and the antiviral response against Japanese encephalitis virus.

作者信息

Li Chenxi, Di Di, Wang Xin, Xia Qiqi, Wahaab Abdul, Anwar Muhammad Naveed, Li Zongjie, Liu Ke, Shao Donghua, Qiu Yafeng, Wei Jianchao, Li Beibei, Ma Zhiyong

机构信息

Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, No.518, Ziyue Road, Shanghai, 200241, PR China.

Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, No.518, Ziyue Road, Shanghai, 200241, PR China.

出版信息

Dev Comp Immunol. 2020 Mar;104:103535. doi: 10.1016/j.dci.2019.103535. Epub 2019 Nov 5.

Abstract

Karyopherin α4 (KPNA4) is an adaptor molecule that mediates type I interferon (IFN) production by facilitating the nuclear translocation of IFN transcription factors. Here, we cloned the duck KPNA4 (duKPNA4) gene and analyzed its involvement in type I IFN expression as well as antiviral response against Japanese encephalitis virus (JEV). The full-length duKPNA4 gene encoded a 520-amino acid protein that shared 97.3-98.7% sequence similarity with its orthologues in chickens, humans and mice. The duKPNA4 was extensively expressed in various duck tissues at the mRNA level. Analysis of the subcellular localization of duKPNA4 by immunofluorescence assays indicated that the duKPNA4 was primarily distributed in both the cytoplasm and nucleus in primary duck embryonic fibroblasts (DEFs). However, it translocated from the cytoplasm to the nucleus in response to poly(I:C) stimulation or JEV infection. The duKPNA4 interacted with duck IFN regulatory factor 7 and facilitated its nuclear translocation, thereby up-regulating the expression of IFN-α and IFN-β in DEFs in the presence of poly(I:C) stimulation. Exogenous expression of duKPNA4 significantly elevated the expression of IFN-α and IFN-β induced by JEV infection and inhibited JEV replication in DEFs. These data demonstrate the importance of duKPNA4 in type I IFN signaling as well as the antiviral response against JEV replication.

摘要

核转运蛋白α4(KPNA4)是一种衔接分子,通过促进干扰素转录因子的核转位来介导I型干扰素(IFN)的产生。在此,我们克隆了鸭KPNA4(duKPNA4)基因,并分析了其在I型干扰素表达以及针对日本脑炎病毒(JEV)的抗病毒反应中的作用。duKPNA4基因全长编码一个520个氨基酸的蛋白质,与鸡、人和小鼠中的同源物具有97.3 - 98.7%的序列相似性。duKPNA4在mRNA水平上在鸭的各种组织中广泛表达。通过免疫荧光分析对duKPNA4进行亚细胞定位表明,duKPNA4主要分布在原代鸭胚成纤维细胞(DEFs)的细胞质和细胞核中。然而,在受到聚肌胞苷酸(poly(I:C))刺激或JEV感染时,它从细胞质转位到细胞核。duKPNA4与鸭干扰素调节因子7相互作用并促进其核转位,从而在存在poly(I:C)刺激的情况下上调DEFs中IFN-α和IFN-β的表达。duKPNA4的外源表达显著提高了JEV感染诱导的IFN-α和IFN-β的表达,并抑制了DEFs中JEV的复制。这些数据证明了duKPNA4在I型干扰素信号传导以及针对JEV复制的抗病毒反应中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5220/7102526/c68cdf2c9f9f/gr1_lrg.jpg

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