Petrovskis E A, Timmins J G, Armentrout M A, Marchioli C C, Yancey R J, Post L E
J Virol. 1986 Aug;59(2):216-23. doi: 10.1128/JVI.59.2.216-223.1986.
The DNA sequence was determined for a region of the pseudorabies virus (PRV) genome to which a mutation defining resistance to a monoclonal antibody has been mapped (M. W. Wathen and L. M. K. Wathen, J. Virol., 51:57-62, 1984). This sequence was found to contain an open reading frame that did not include an amino acid sequence directing N-linked glycosylation. This open reading frame was expressed in uninfected Chinese hamster ovary cells to produce the PRV glycoprotein gp50. When PRV-infected Vero cells were incubated in the presence of tunicamycin, the gp50 that was produced had an identical molecular weight to that produced in the absence of drug. When infected cells were incubated in the presence of monensin, the molecular weight of gp50 was reduced from 60,000 to 45,000, but was not sensitive to endo-beta-N-acetylglucosaminidase H. These observations led to the conclusion that gp50 does not contain N-linked carbohydrate, as predicted from the DNA sequence. A region of the amino acid sequence and the positions of the cysteine residues of PRV gp50 are homologous to glycoprotein D of herpes simplex virus.
测定了伪狂犬病病毒(PRV)基因组中一个区域的DNA序列,对单克隆抗体具有抗性的一个突变已定位到该区域(M. W. 沃森和L. M. K. 沃森,《病毒学杂志》,51:57 - 62,1984年)。发现该序列包含一个开放阅读框,其中不包括指导N - 连接糖基化的氨基酸序列。这个开放阅读框在未感染的中国仓鼠卵巢细胞中表达,产生PRV糖蛋白gp50。当PRV感染的非洲绿猴肾细胞在衣霉素存在下培养时,产生的gp50的分子量与在无药物情况下产生的相同。当感染细胞在莫能菌素存在下培养时,gp50的分子量从60,000降至45,000,但对内切β - N - 乙酰葡糖胺酶H不敏感。这些观察结果得出结论,如从DNA序列预测的那样,gp50不含有N - 连接的碳水化合物。PRV gp50的氨基酸序列区域和半胱氨酸残基的位置与单纯疱疹病毒的糖蛋白D同源。