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樱桃叶卷线虫传多角体病毒白桦分离株(I2)外壳蛋白编码区的鉴定、克隆及序列分析

The identification, cloning, and sequence analysis of the coat protein coding region of a birch isolate (I2) of cherry leaf roll nepovirus.

作者信息

Scott N W, Cooper J I, Edwards M L

机构信息

Institute of Virology and Environmental Microbiology, Oxford, U.K.

出版信息

Arch Virol. 1993;131(1-2):209-15. doi: 10.1007/BF01379093.

DOI:10.1007/BF01379093
PMID:8328915
Abstract

The coat protein gene of RNA-2 of cherry leaf roll nepovirus (CLRV) birch isolate I2 was cloned, identified, and sequenced. Transcripts derived from cDNA to the coat protein gene made a polypeptide of M(r) 51.5 k when translated in vitro. The predicted amino acid sequence of the coat protein showed little identity with nepoviruses having small RNA-2s. It did, however, have 27% sequence identity with the coat protein of tomato ringspot nepovirus which, like CLRV, has a relatively large RNA-2.

摘要

克隆、鉴定并测序了樱桃卷叶线虫传多面体病毒(CLRV)桦树分离株I2的RNA - 2外壳蛋白基因。从外壳蛋白基因的cDNA转录而来的转录本在体外翻译时产生了一个分子量为51.5k的多肽。外壳蛋白的预测氨基酸序列与具有小RNA - 2的线虫传多面体病毒几乎没有同源性。然而,它与番茄环斑线虫传多面体病毒的外壳蛋白有27%的序列同源性,番茄环斑线虫传多面体病毒与CLRV一样,具有相对较大的RNA - 2。

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本文引用的文献

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Expression of Middle-Component RNA of Cowpea Mosaic Virus: In Vitro Generation of a Precursor to Both Capsid Proteins by a Bottom-Component RNA-Encoded Protease from Infected Cells.豇豆花叶病毒中间组分RNA的表达:感染细胞中由底部组分RNA编码的蛋白酶体外产生两种衣壳蛋白的前体
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从电转印到聚偏二氟乙烯膜上的皮摩尔量蛋白质中获得的序列。
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Fast and sensitive multiple sequence alignments on a microcomputer.在微型计算机上进行快速且灵敏的多序列比对。
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RNA2 of grapevine fanleaf virus: sequence analysis and coat protein cistron location.葡萄扇叶病毒的RNA2:序列分析及外壳蛋白顺反子定位
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