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伪狂犬病病毒dUTP酶的鉴定与特性分析

Identification and characterization of pseudorabies virus dUTPase.

作者信息

Jöns A, Mettenleiter T C

机构信息

Institute of Molecular and Cellular Virology, Friedrich-Loeffler-Institutes, Insel Riems, Germany.

出版信息

J Virol. 1996 Feb;70(2):1242-5. doi: 10.1128/JVI.70.2.1242-1245.1996.

Abstract

Sequence analysis within the long segment of the pseudorabies virus (PrV) genome identified an open reading frame of 804 bp whose deduced protein product of 268 amino acids exhibited homology to dUTPases of other herpesviruses. The gene was designated UL50 because of its colinearity with the homologous gene of herpes simplex virus type 1. An antiserum raised against a bacterially expressed fragment of PrV UL50 specifically detected a 33-kDa protein in lysates of infected cells, which is in agreement with the predicted molecular mass of the PrV UL50 protein. A UL50-negative PrV mutant (PrV UL50-) was constructed by the insertion of a beta-galactosidase expression cassette into the UL50 coding sequence. A corresponding rescuant (PrV UL50resc) was also isolated. The interruption of the UL50 gene led to the disappearance of the 33-kDa protein, whereas restoration of UL50 gene expression restored detection of the 33-kDa protein. Enzyme activity assays confirmed that UL50 of PrV codes for a dUTPase which copurifies with nuclei of infected cells. PrV UL50- replicated with an only slightly reduced efficiency in epithelial cells in culture compared with that of its parental wild-type virus strain. Our results thus demonstrate that UL50 of PrV encodes a protein of 33 kDa with dUTPase activity which copurifies with nuclei of infected cells and is dispensable for replication in cultured epithelial cells.

摘要

对伪狂犬病病毒(PrV)基因组的长片段进行序列分析时,鉴定出一个804 bp的开放阅读框,其推导的268个氨基酸的蛋白质产物与其他疱疹病毒的dUTP酶具有同源性。由于该基因与1型单纯疱疹病毒的同源基因具有共线性,因此被命名为UL50。针对PrV UL50的细菌表达片段制备的抗血清在感染细胞的裂解物中特异性检测到一种33 kDa的蛋白质,这与PrV UL50蛋白的预测分子量相符。通过将β-半乳糖苷酶表达盒插入UL50编码序列构建了一个UL50阴性的PrV突变体(PrV UL50-)。还分离出了相应的拯救病毒(PrV UL50resc)。UL50基因的中断导致33 kDa蛋白质消失,而UL50基因表达的恢复则恢复了对33 kDa蛋白质的检测。酶活性测定证实,PrV的UL50编码一种dUTP酶,该酶与感染细胞核共纯化。与亲代野生型病毒株相比,PrV UL50-在培养的上皮细胞中的复制效率仅略有降低。因此,我们的结果表明,PrV的UL50编码一种具有dUTP酶活性的33 kDa蛋白质,该蛋白质与感染细胞核共纯化,并且在培养的上皮细胞中复制时是可有可无的。

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