Okuno Toshiomi, Jiang Yun Bao, Ueda Keiji, Nishimura Ken, Tamura Toshihide, Yamanishi Koichi
Department of Bacteriology, Hyogo College of Medicine, 1-1, Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan.
Virus Res. 2002 Dec;90(1-2):77-89. doi: 10.1016/s0168-1702(02)00142-9.
Open reading frame (ORF) 50 of human herpesvirus 8 (HHV8, Kaposi's sarcoma-associated herpesvirus) is one of the immediate-early gene and a homologue of BRLF1 gene of Epstein-Barr virus. It encodes a key switch protein to trigger viral lytic replication from latency. We have established several hybridoma clones producing monoclonal antibodies (MAbs) to the products of HHV8 ORFs. Using these antibodies, we analyzed antigen expression in a HHV8 infected cell line after treatment with phorbol ester (12-O-tetradecanoylphorbol-13-acetate, TPA). A MAb reacted to 110 kilodalton (kDa) and 62 kDa proteins encoded by ORF50 (ORF50 protein). Kinetic studies of antigen expression by Western blotting revealed that ORF50 protein was induced as early as 6 h after TPA treatment. The proteins encoded by ORFK3, ORFK5, ORFK9, ORF59 and ORFK8.1 were not detected earlier than ORF50 protein. However, when antigen positive cells were counted by immunofluorescent antibody (IFA) test, number of ORFK5 protein positive cells were higher than that of ORF50 protein positive cells at all time after TPA or mock treatment. To confirm the results of IFA test, individual cell was analyzed by reverse transcription polymerase chain reaction. Some cells expressed ORFK5 transcript but not ORF50 transcript. Therefore, we concluded that, although ORF50 protein is a key switch protein of ORFK3, ORFK9, ORF59 and ORFK8.1 expression, it is not essential to trigger ORFK5 gene.
人类疱疹病毒8型(HHV8,即卡波西肉瘤相关疱疹病毒)的开放阅读框(ORF)50是一种立即早期基因,是爱泼斯坦-巴尔病毒BRLF1基因的同源物。它编码一种关键的开关蛋白,以触发病毒从潜伏期进入裂解复制。我们已经建立了几个产生针对HHV8 ORF产物的单克隆抗体(MAb)的杂交瘤克隆。使用这些抗体,我们分析了用佛波酯(12-O-十四酰佛波醇-13-乙酸酯,TPA)处理后HHV8感染细胞系中的抗原表达。一种单克隆抗体与ORF50编码的110千道尔顿(kDa)和62 kDa蛋白发生反应(ORF50蛋白)。通过蛋白质印迹对抗原表达的动力学研究表明,ORF50蛋白在TPA处理后6小时就被诱导产生。ORFK3、ORFK5、ORFK9、ORF59和ORFK8.1编码的蛋白比ORF50蛋白更早未被检测到。然而,当通过免疫荧光抗体(IFA)试验对抗原阳性细胞进行计数时,在TPA或模拟处理后的所有时间,ORFK5蛋白阳性细胞的数量都高于ORF50蛋白阳性细胞。为了证实IFA试验的结果,通过逆转录聚合酶链反应对单个细胞进行了分析。一些细胞表达ORFK5转录本但不表达ORF50转录本。因此,我们得出结论,尽管ORF50蛋白是ORFK3、ORFK9、ORF59和ORFK8.1表达的关键开关蛋白,但它对于触发ORFK5基因并非必不可少。