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流感病毒基因组的体外复制:RNA复制酶与病毒感染细胞核糖核蛋白复合物的选择性解离

Replication in vitro of the influenza virus genome: selective dissociation of RNA replicase from virus-infected cell ribonucleoprotein complexes.

作者信息

Toyoda T, Kobayashi M, Ishihama A

机构信息

Department of Molecular Genetics, National Institute of Genetics, Shizuoka, Japan.

出版信息

Arch Virol. 1994;136(3-4):269-86. doi: 10.1007/BF01321057.

Abstract

Replication of the influenza virus genome involves two discrete step reactions: vRNA-directed primer-independent (unprimed) synthesis of cRNA; and cRNA-directed unprimed synthesis of vRNA. Nuclear extracts from both MDCK and HeLa cells infected with influenza virus A/PR8/34 exhibited unprimed synthesis of both cRNA and vRNA strands (a parameter of RNA replication). Ribonucleoprotein (RNP) complexes with the replication activity were isolated from these nuclear extracts by glycerol gradient centrifugation in the presence of 0.1 M KCl. At 0.5 M KCl, however, these complexes were dissociated into stripped RNP and soluble protein fractions. The soluble fraction contained the activity of exogenous template-dependent unprimed RNA synthesis, indicating that the RNA replicase is dissociated from RNP upon exposure to high salt concentrations. On the other hand, the high salt-treated RNP catalyzed only primer-dependent RNA synthesis, but regained a low level activity of exogenous template-dependent unprimed RNA synthesis by adding nuclear extracts from uninfected cells, suggesting that host factor(s) is involved in the functional interconversion of influenza virus RNA polymerase.

摘要

流感病毒基因组的复制涉及两个离散的步骤反应

vRNA 指导的不依赖引物(无引物)的 cRNA 合成;以及 cRNA 指导的不依赖引物的 vRNA 合成。感染甲型流感病毒 A/PR8/34 的 MDCK 和 HeLa 细胞的核提取物均表现出 cRNA 和 vRNA 链的无引物合成(RNA 复制的一个参数)。在 0.1 M KCl 存在下,通过甘油梯度离心从这些核提取物中分离出具有复制活性的核糖核蛋白(RNP)复合物。然而,在 0.5 M KCl 时,这些复合物解离成脱蛋白的 RNP 和可溶性蛋白组分。可溶性组分含有外源模板依赖性无引物 RNA 合成的活性,表明 RNA 复制酶在暴露于高盐浓度时从 RNP 上解离。另一方面,高盐处理的 RNP 仅催化依赖引物的 RNA 合成,但通过添加未感染细胞的核提取物恢复了低水平的外源模板依赖性无引物 RNA 合成活性,这表明宿主因子参与了流感病毒 RNA 聚合酶的功能相互转换。

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