Liang X, Chow B, Li Y, Raggo C, Yoo D, Attah-Poku S, Babiuk L A
Veterinary Infectious Diseases Organization, University of Saskatchewan, Saskatoon, Canada.
J Virol. 1995 Jun;69(6):3863-7. doi: 10.1128/JVI.69.6.3863-3867.1995.
The sequence of the bovine herpesvirus 1 (BHV-1) gene that is homologous to the herpes simplex virus UL49 gene was determined. The BHV-1 UL49 homolog open reading frame consists of 774 bp and is capable of encoding 258 amino acids. Northern (RNA) blot analysis showed that the BHV-1 UL49 homolog is transcribed into a 1.1-kb RNA which is coterminal with the transcripts of an upstream UL49.5 homolog gene. Rabbit antisera produced against synthetic peptides of the predicted UL49 homolog gene product recognized a polypeptide of 33 to 35 kDa in both virus-infected cells and isolated virions. Further analysis by unionic-detergent partition of isolated virions suggested that the UL49 homolog gene product is a virion tegument protein. Indirect immunofluorescence assay revealed that the UL49 homolog gene product was predominantly localized in the nuclei of BHV-1-infected cells. A mutant virus with the UL49 homolog gene deleted was produced, and it was able to replicate in noncomplementing cells. Nevertheless, the yield of mutant virus was significantly reduced. The results from this study suggest that the BHV-1 UL49 homolog gene encodes a nuclear protein which constitutes a tegument component in mature virions and that it is dispensable for virus growth in cell culture.
确定了与单纯疱疹病毒UL49基因同源的牛疱疹病毒1型(BHV-1)基因的序列。BHV-1 UL49同源开放阅读框由774个碱基对组成,能够编码258个氨基酸。Northern(RNA)印迹分析表明,BHV-1 UL49同源物被转录成一种1.1 kb的RNA,它与上游UL49.5同源基因的转录本共末端。针对预测的UL49同源基因产物的合成肽产生的兔抗血清在病毒感染的细胞和分离的病毒粒子中都识别出一种33至35 kDa的多肽。对分离的病毒粒子进行非离子去污剂分配的进一步分析表明,UL49同源基因产物是一种病毒粒子被膜蛋白。间接免疫荧光试验显示,UL49同源基因产物主要定位于BHV-1感染细胞的细胞核中。产生了一个缺失UL49同源基因的突变病毒,它能够在非互补细胞中复制。然而,突变病毒的产量显著降低。本研究结果表明,BHV-1 UL49同源基因编码一种核蛋白,该蛋白构成成熟病毒粒子中的被膜成分,并且它对于病毒在细胞培养中的生长是可有可无的。