在巴布亚新几内亚高地发现的一种新的JC病毒变体在agnoprotein基因中有21个碱基对的缺失。

Journal of human virology Pub Date : 1999-11-01
D V Jobes, J S Friedlaender, C S Mgone, G Koki, M P Alpers, C F Ryschkewitsch, G L Stoner
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引用次数: 0

摘要

目的:本文描述了从巴布亚新几内亚高地恢复的一种独特的JC病毒(JCV)变体,该变体含有agnoprotein基因在框内21 bp的缺失。我们描述了突变的特征,并提出了缺失在JCV进化中的可能作用。研究设计/方法:从尿液中提取JCV DNA,用全基因组引物进行聚合酶链反应(PCR)扩增。对PCR产物进行克隆,并对多个克隆进行测序。PCR扩增了JCV的agnogene,以验证agnogene缺失的存在。结果:该突变在3'端附近产生了一个21 bp的缺失,这改变了预测的信使RNA的二级结构,并改变了agnogene 3'端的局部密码子使用。蛋白质二级结构预测表明,agnoprotein的缺失部分可能是一个灵活的表面特征。结论:我们描述了JCV中第一个稳定的编码区缺失,这可能意味着导致其他高地病毒群分裂的单一进化事件,并且发生在人类扩张导致西南太平洋人类居住之后。
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A novel JC virus variant found in the Highlands of Papua New Guinea has a 21-base pair deletion in the agnoprotein gene.

Objectives: This paper describes a unique JC virus (JCV) variant recovered from the Highlands of Papua New Guinea that contains an inframe 21-bp deletion in the agnoprotein gene. We characterize the mutation and suggest possible roles for the deletion in JCV evolution.

Study design/methods: JCV DNA was extracted from urine and polymerase chain reaction (PCR) amplified using whole genome primers. PCR products were cloned, and multiple clones were sequenced. The JCV agnogene was PCR amplified to verify the presence of the agnogene deletion.

Results: This mutation creates a 21-bp deletion near the 3' end, which alters the predicted secondary structure of the messenger RNA and changes local codon usage at the 3' end of the agnogene. Protein secondary structure predictions suggest the deleted portion of the agnoprotein may be a flexible surface feature.

Conclusions: We describe the first stable coding region deletion in JCV that presumably signifies a single evolutionary event that led to the split from other Highlands viral groups and occurred well after the human expansions that led to the peopling of the Southwest Pacific.

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