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动物弹状病毒的结构-功能关系及复制模式

Structure-function relationships and mode of replication of animal rhabdoviruses.

作者信息

Sokol F, Koprowski H

出版信息

Proc Natl Acad Sci U S A. 1975 Mar;72(3):933-6. doi: 10.1073/pnas.72.3.933.

DOI:10.1073/pnas.72.3.933
PMID:165494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC432436/
Abstract

Recently accumulated knowledge allows more precise comparison of the structural (and possibly evolutionary) relationships of several different animal rhabdoviruses: vesicular stomatitis virus, rabies virus, Kern Canyon virus, and spring viremia of carp virus. Each virus is composed primarily of a glycoprotein, an RNA-associated nucleoprotein, and one or two membrane proteins. Vesicular stomatitis virus group viruses contain lesser amounts of two additional distinct polypeptides, NS and L. The separate viruses undergo structural polypeptide phosphorylation in vivo according to characteristic patterns. In vesicular stomatitis virus the NS protein is selectively phosphorylated. In rabies group viruses and in spring viremia of carp virus, the nucleoprotein is the predominant phosphoprotein; in these viruses only the phosphorylated moiety is selectively cleaved off with trypsin. In Kern Canyon virus, only membrane protein and glycoprotein are weakly phosphorylated. Each virus possesses a virion-bound protein kinase. Vesicular stomatitis virus group viruses, Kern Canyon virus, and spring viremia of carp virus only contain virion-bound transcriptases of respectively decreasing levels of activity demonstrable in vitro. Vesicular stomatitis and Kern Canyon viruses replicate efficiently in enucleated cells; rabies virus does not. Based upon these observations, it is suggested that vesicular stomatitis virus may represent the most highly evolved of these rhabdoviruses, whereas spring viremia of carp and Kern Canyon viruses may represent "evolutionary links" between the vesicular stomatitis and rabies virus groups.

摘要

最近积累的知识使人们能够更精确地比较几种不同动物弹状病毒的结构(以及可能的进化)关系:水疱性口炎病毒、狂犬病病毒、克恩峡谷病毒和鲤鱼春季病毒血症病毒。每种病毒主要由一种糖蛋白、一种与RNA相关的核蛋白以及一种或两种膜蛋白组成。水疱性口炎病毒群病毒还含有少量另外两种不同的多肽,即NS和L。这些不同的病毒在体内会根据特定模式进行结构多肽磷酸化。在水疱性口炎病毒中,NS蛋白被选择性磷酸化。在狂犬病病毒群病毒和鲤鱼春季病毒血症病毒中,核蛋白是主要的磷蛋白;在这些病毒中,只有磷酸化部分能被胰蛋白酶选择性切割。在克恩峡谷病毒中,只有膜蛋白和糖蛋白被微弱磷酸化。每种病毒都拥有一种与病毒粒子结合的蛋白激酶。水疱性口炎病毒群病毒、克恩峡谷病毒和鲤鱼春季病毒血症病毒只含有与病毒粒子结合的转录酶,其体外可检测到的活性水平依次降低。水疱性口炎病毒和克恩峡谷病毒能在去核细胞中高效复制;狂犬病病毒则不能。基于这些观察结果,有人提出水疱性口炎病毒可能代表了这些弹状病毒中进化程度最高的,而鲤鱼春季病毒血症病毒和克恩峡谷病毒可能代表了水疱性口炎病毒群和狂犬病病毒群之间的“进化联系”。

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Synthesis of globin RNA in enucleated differentiating murine erythroleukemia cells.去核分化小鼠红白血病细胞中珠蛋白RNA的合成
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4
Rabies pathogenesis.狂犬病发病机制。
Arch Virol. 1977;54(4):279-97. doi: 10.1007/BF01314774.

本文引用的文献

1
Biochemical and biophysical studies on the nucleocapsid and on the RNA of rabies virus.狂犬病病毒核衣壳及RNA的生化与生物物理研究
Virology. 1969 Aug;38(4):651-65. doi: 10.1016/0042-6822(69)90184-6.
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Antigenic properties of rabies virus components.狂犬病病毒成分的抗原特性。
J Immunol. 1973 Jan;110(1):269-76.
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Phosphoproteins, structural components of rhabdoviruses.磷蛋白,弹状病毒的结构成分。
Virology. 1973 Mar;52(1):246-63. doi: 10.1016/0042-6822(73)90413-3.
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Structural phosphoproteins associated with ten rhabdoviruses.与十种弹状病毒相关的结构磷蛋白。
J Gen Virol. 1974 Sep;24(3):433-45. doi: 10.1099/0022-1317-24-3-433.
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Rhabdovirus replication in enucleated host cells.弹状病毒在去核宿主细胞中的复制。
J Virol. 1974 Aug;14(2):300-6. doi: 10.1128/JVI.14.2.300-306.1974.
6
Phosphate acceptor amino acid residues in structural proteins of rhabdoviruses.弹状病毒结构蛋白中的磷酸受体氨基酸残基
J Virol. 1974 Jul;14(1):145-51. doi: 10.1128/JVI.14.1.145-151.1974.
7
RNA transcription by the virion polymerases of five rhabdoviruses.五种弹状病毒的病毒粒子聚合酶进行的RNA转录
J Virol. 1974 Mar;13(3):652-61. doi: 10.1128/JVI.13.3.652-661.1974.
8
Comparative electrophoretic analysis of the virus proteins of four rhabdoviruses.四种弹状病毒病毒蛋白的比较电泳分析
J Gen Virol. 1974 Jan;22(1):21-33. doi: 10.1099/0022-1317-22-1-21.
9
Detection of homologous RNA sequences among six rhabdovirus genomes.六种弹状病毒基因组中同源RNA序列的检测
J Virol. 1974 Jan;13(1):250-2. doi: 10.1128/JVI.13.1.250-252.1974.
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Protein kinase and phosphoproteins of vesicular stomatitis virus.水疱性口炎病毒的蛋白激酶和磷酸化蛋白
J Virol. 1974 Jan;13(1):113-24. doi: 10.1128/JVI.13.1.113-124.1974.