MacLean C A, Robertson L M, Jamieson F E
MRC Virology Unit, University of Glasgow, U.K.
J Gen Virol. 1993 Jun;74 ( Pt 6):975-83. doi: 10.1099/0022-1317-74-6-975.
On the basis of predicted amino acid sequence characteristics, herpes simplex virus type 1 gene UL10 is thought likely to encode a membrane protein with eight potential transmembrane regions. Previously, a protein with an apparent M(r) 47,000 on SDS-PAGE was identified as a product of this gene. Here we have further characterized this protein, and show that it is modified by N-linked glycosylation, associates with membranes from infected cells, and is a component of the virus particle. It is not essential for virus growth in tissue culture. To investigate its role in vivo a deletion mutant lacking the majority of the UL10 open reading frame was constructed (UL10-del). The in vitro growth properties of this virus were consistent with previous studies; it grew to give slightly lower yields than wild-type and revertant viruses, and had no apparent temperature-sensitive or host range phenotype. In vivo, in a mouse model, UL10-del was capable of establishing a latent infection, although it was impaired for growth at the periphery, and for spread to and/or growth within the nervous system relative to wild-type or revertant viruses.
基于预测的氨基酸序列特征,单纯疱疹病毒1型基因UL10被认为可能编码一种具有八个潜在跨膜区域的膜蛋白。此前,在SDS-PAGE上表观分子量为47,000的一种蛋白质被鉴定为该基因的产物。在此,我们对这种蛋白质进行了进一步表征,结果表明它会发生N-连接糖基化修饰,与感染细胞的膜相关联,并且是病毒粒子的一个组成部分。它对于病毒在组织培养中的生长并非必需。为了研究其在体内的作用,构建了一个缺失大部分UL10开放阅读框的缺失突变体(UL10-del)。该病毒的体外生长特性与先前的研究一致;其生长产生的产量略低于野生型和回复病毒,并且没有明显的温度敏感或宿主范围表型。在体内,在小鼠模型中,UL10-del能够建立潜伏感染,尽管相对于野生型或回复病毒,它在外周的生长以及向神经系统扩散和/或在神经系统内生长方面存在缺陷。