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牛细小病毒的完整核苷酸序列及基因组结构

Complete nucleotide sequence and genome organization of bovine parvovirus.

作者信息

Chen K C, Shull B C, Moses E A, Lederman M, Stout E R, Bates R C

出版信息

J Virol. 1986 Dec;60(3):1085-97. doi: 10.1128/JVI.60.3.1085-1097.1986.

Abstract

We determined the complete nucleotide sequence of bovine parvovirus (BPV), an autonomous parvovirus. The sequence is 5,491 nucleotides long. The terminal regions contain nonidentical imperfect palindromic sequences of 150 and 121 nucleotides. In the plus strand, there are three large open reading frames (left ORF, mid ORF, and right ORF) with coding capacities of 729, 255, and 685 amino acids, respectively. As with all parvoviruses studied to date, the left ORF of BPV codes for the nonstructural protein NS-1 and the right ORF codes for the major parts of the three capsid proteins. The mid ORF probably encodes the major part of the nonstructural protein NP-1. There are promoterlike sequences at map units 4.5, 12.8, and 38.7 and polyadenylation signals at map units 61.6, 64.6, and 98.5. BPV has little DNA homology with the defective parvovirus AAV, with the human autonomous parvovirus B19, or with the other autonomous parvoviruses sequenced (canine parvovirus, feline panleukopenia virus, H-1, and minute virus of mice). Even though the overall DNA homology of BPV with other parvoviruses is low, several small regions of high homology are observed when the amino acid sequences encoded by the left and right ORFs are compared. From these comparisons, it can be shown that the evolutionary relationship among the parvoviruses is B19 in equilibrium with AAV in equilibrium with BPV in equilibrium with MVM. The highly conserved amino acid sequences observed among all parvoviruses may be useful in the identification and detection of parvoviruses and in the design of a general parvovirus vaccine.

摘要

我们测定了自主细小病毒牛细小病毒(BPV)的完整核苷酸序列。该序列长5491个核苷酸。末端区域包含150和121个核苷酸的不相同的不完全回文序列。在正链上,有三个大的开放阅读框(左ORF、中ORF和右ORF),编码能力分别为729、255和685个氨基酸。与迄今研究的所有细小病毒一样,BPV的左ORF编码非结构蛋白NS-1,右ORF编码三种衣壳蛋白的主要部分。中ORF可能编码非结构蛋白NP-1的主要部分。在图谱单位4.5、12.8和38.7处有类似启动子的序列,在图谱单位61.6、64.6和98.5处有聚腺苷酸化信号。BPV与缺陷细小病毒AAV、人类自主细小病毒B19或其他已测序的自主细小病毒(犬细小病毒、猫泛白细胞减少症病毒、H-1和小鼠微小病毒)的DNA同源性很低。尽管BPV与其他细小病毒的总体DNA同源性较低,但在比较左ORF和右ORF编码的氨基酸序列时,观察到几个高度同源的小区域。从这些比较中可以看出,细小病毒之间的进化关系是B19与AAV平衡,AAV与BPV平衡,BPV与MVM平衡。在所有细小病毒中观察到的高度保守的氨基酸序列可能有助于细小病毒的鉴定和检测以及通用细小病毒疫苗的设计。

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本文引用的文献

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