Rahman Md Masmudur, Gopinathan Karumathil P
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India.
Virus Res. 2003 Jul;94(1):45-57. doi: 10.1016/s0168-1702(03)00123-0.
We describe here the characterization of the gene gp64 encoding the envelope fusion protein GP64 (open reading frame) ORF 105 from Bombyx mori nucleopolyhedrovirus (BmNPV). gp64 was transcribed from the early to late stages of infection and the transcripts were seen from 6 to 72 h post infection (hpi). The early transcripts initiated from a consensus CAGT motif while the late transcripts arose from three conserved TAAG motifs, all of which were located in the near upstream region of the coding sequence. Both early and late transcripts terminated at a run of T residues following the second polyadenylation signal located 31 nt downstream of the translation termination codon. BmGP64 protein was detectable from 6 hpi and was present in larger quantities throughout the infection process from 12 hpi, in BmNPV-infected BmN cells. The persistent presence of GP64 in BmN cells differed from the protein expression pattern of GP64 in Autographa californica multinucleocapsid nucleopolyhedrovirus infection, where the protein levels decreased significantly by late times (48 hpi). BmGP64 was located in the membrane and cytoplasm of the infected host cells and as a component of the budded virions. The production of infectious budded virus and the fusion activity were reduced when glycosylation of GP64 was inhibited.
我们在此描述了家蚕核型多角体病毒(BmNPV)包膜融合蛋白GP64(开放阅读框)ORF 105编码基因gp64的特征。gp64在感染的早期至晚期转录,在感染后6至72小时(hpi)可观察到转录本。早期转录本从共有CAGT基序起始,而晚期转录本则从三个保守的TAAG基序产生,所有这些基序均位于编码序列的近上游区域。早期和晚期转录本均在位于翻译终止密码子下游31个核苷酸处的第二个聚腺苷酸化信号后的一串T残基处终止。在受BmNPV感染的BmN细胞中,从感染后6小时开始可检测到BmGP64蛋白,并且从感染后12小时起在整个感染过程中大量存在。BmN细胞中GP64的持续存在不同于苜蓿银纹夜蛾多核衣壳核型多角体病毒感染中GP64的蛋白质表达模式,在后者中,蛋白质水平在后期(感染后48小时)显著下降。BmGP64位于受感染宿主细胞的膜和细胞质中,并作为出芽病毒粒子的一个组分。当GP64的糖基化受到抑制时,感染性出芽病毒的产生和融合活性降低。