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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Infectious salmon anemia virus (ISAV) genomic segment 3 encodes the viral nucleoprotein (NP), an RNA-binding protein with two monopartite nuclear localization signals (NLS).
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Infectious salmon anemia virus (ISAV) genomic segment 3 encodes the viral nucleoprotein (NP), an RNA-binding protein with two monopartite nuclear localization signals (NLS).

机译:传染性鲑鱼贫血病毒(ISAV)基因组片段3编码病毒核蛋白(NP),RNA结合蛋白带有两个单核核定位信号(NLS)。

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摘要

Infectious salmon anemia virus (ISAV) is the type species of the genus Isavirus belonging to the Orthomyxoviridae, and causes serious disease in Atlantic salmon (Salmo salar). This study presents the expression and functional analysis of the ISAV genome segment 3, and provides further evidence that it encodes the viral nucleoprotein (NP). The encoded protein was expressed in a baculovirus system, and Western blot analysis showed that it corresponds to the 66-71kDa structural protein previously found in purified ISAV preparations. RNA-binding activity was established by the interaction of viral and recombinant NP with single-stranded RNA transcribed in vitro. Immunofluorescence studies of infected cells showed the ISAV NP to be an early protein. It locates to the nucleus of infected cells before it is transported to the cytoplasm prior to virus assembly. A similar localization pattern was observed in cells transfected with the NP gene, confirming that the encoded protein has an intrinsic ability to be imported into the nucleus. Two monopartite nuclear localization signals (NLS) at amino acids (230)RPKR(233) and (473)KPKK(476) were identified by computer analysis, and validated by site-directed mutagenesis. In contrast to other orthomyxovirus-NPs, that have several NLSs that function independent of each other, both NLSs had to be present for the ISAV NP protein to be transported into the nucleus, indicating that these motifs cooperate to target the protein to the nucleus.
机译:传染性鲑鱼贫血病毒(ISAV)是属于正粘病毒科的艾萨病毒属的类型种,在大西洋鲑鱼(Salmo salar)中引起严重的疾病。这项研究介绍了ISAV基因组片段3的表达和功能分析,并提供了进一步的证据证明它编码了病毒核蛋白(NP)。编码的蛋白在杆状病毒系统中表达,Western印迹分析表明它对应于先前在纯化的ISAV制剂中发现的66-71kDa结构蛋白。 RNA结合活性是通过病毒和重组NP与体外转录的单链RNA相互作用而建立的。感染细胞的免疫荧光研究表明,ISAV NP是一种早期蛋白质。它在病毒组装之前先被定位到受感染细胞的核,然后再被转运到细胞质。在用NP基因转染的细胞中观察到了相似的定位模式,这证实了编码的蛋白具有被导入细胞核的内在能力。通过计算机分析鉴定了氨基酸(230)RPKR(233)和(473)KPKK(476)上的两个单核核定位信号(NLS),并通过定点诱变进行了验证。与具有几个彼此独立运作的NLS的正粘病毒NP相比,必须同时存在两个NLS才能将ISAV NP蛋白转运到细胞核中,这表明这些基序协同作用将蛋白质靶向细胞核。

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