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西尼罗河黄病毒基因组区域的一级结构,该区域编码所有非结构蛋白。

Primary structure of the West Nile flavivirus genome region coding for all nonstructural proteins.

作者信息

Castle E, Leidner U, Nowak T, Wengler G, Wengler G

出版信息

Virology. 1986 Feb;149(1):10-26. doi: 10.1016/0042-6822(86)90082-6.

Abstract

The genome RNA of the flavivirus West Nile (WN) virus has been transcribed into cDNA, the cDNA has been cloned, and the nucleotide sequences coding for the structural proteins have been determined (Castle et al., 1985; Wengler et al., 1985). We have now determined the nucleotide sequence coding for all viral nonstructural proteins which comprises 7929 nucleotides. Together with our earlier sequence analyses these data show that a long open reading frame (ORF) containing 10,290 nucleotides is present on the genome of WN virus. The two largest nonstructural proteins which can be detected in flavivirus-infected cells are the proteins NV5 and NV4 which have an apparent molecular mass of 97,000 and 74,000 Da, respectively. Both proteins were isolated by preparative polyacrylamide gel electrophoresis, and partial amino acid sequences of peptides derived from these proteins were determined. These analyses allow us to localize the nucleotide regions which code for these proteins and show that the region coding for the NV5 protein is located at the 3'-terminus of the long ORF. Together with our earlier analyses these data show that the protein sequences of virus-specific proteins are present on the viral polyprotein translated from the long ORF in the order V2-NV2-V3-(nonstructural proteins of up to 75,000 Da)-NV4-(nonstructural proteins of up to 45,000 Da)-NV5. Our data indicate that virus-specific structural and nonstructural proteins which are synthesized from a single long ORF accumulate in large amounts in infected cells. A possible role of the presence of these molecules, which are associated to cellular membranes, in the accumulation of membrane vesicles which characteristically occurs in flavivirus-infected cells is discussed.

摘要

黄病毒西尼罗河(WN)病毒的基因组RNA已被转录成cDNA,该cDNA已被克隆,并且编码结构蛋白的核苷酸序列已被确定(Castle等人,1985年;Wengler等人,1985年)。我们现已确定了编码所有病毒非结构蛋白的核苷酸序列,该序列由7929个核苷酸组成。连同我们早期的序列分析,这些数据表明WN病毒基因组上存在一个包含10290个核苷酸的长开放阅读框(ORF)。在黄病毒感染细胞中可检测到的两种最大的非结构蛋白是NV5和NV4蛋白,其表观分子量分别为97000和74000道尔顿。这两种蛋白均通过制备性聚丙烯酰胺凝胶电泳分离,并测定了源自这些蛋白的肽段的部分氨基酸序列。这些分析使我们能够定位编码这些蛋白的核苷酸区域,并表明编码NV5蛋白的区域位于长ORF的3'末端。连同我们早期的分析,这些数据表明病毒特异性蛋白的蛋白序列以V2-NV2-V3-(高达75000道尔顿的非结构蛋白)-NV4-(高达45000道尔顿的非结构蛋白)-NV5的顺序存在于从长ORF翻译的病毒多蛋白上。我们的数据表明,从单个长ORF合成的病毒特异性结构和非结构蛋白在感染细胞中大量积累。讨论了这些与细胞膜相关的分子的存在在黄病毒感染细胞中典型出现的膜泡积累中的可能作用。

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