Habib S, Hasnain S E
Membrane Biology Division, Central Drug Research Institute, Chattar Manzil, Lucknow-226001, India.
J Virol. 2000 Jun;74(11):5182-9. doi: 10.1128/jvi.74.11.5182-5189.2000.
The identification of potential baculovirus origins of replication (ori) has involved the generation and characterization of defective interfering particles that contain major genomic deletions yet retain their capability to replicate by testing the replication ability of transiently transfected plasmids carrying viral sequences in infected cells. So far, there has not been any evidence to demonstrate the actual utilization of these putative origins in Autographa californica multinucleocapsid nuclear polyhedrosis virus (AcMNPV) replication. By using the method of origin mapping by competitive PCR, we have obtained quantitative data for the ori activity of the HindIII-K region and the ie-1 promoter sequence in AcMNPV. We also provide evidence for differential activity of the two ori in the context of the viral genome through the replication phase of viral infection. Comparison of the number of molecules representing the HindIII-K and ie-1 origins vis-à-vis the non-ori polH region in a size-selected nascent DNA preparation revealed that the HindIII-K ori is utilized approximately 14 times more efficiently than the ie-1 region during the late phase of infection. HindIII-K also remains the more active ori through the early and middle replication phases. Our results provide in vivo evidence in support of the view that AcMNPV replication involves multiple ori that are activated with vastly different efficiencies during the viral infection cycle.
杆状病毒潜在复制起点(ori)的鉴定工作涉及缺陷干扰颗粒的产生和特性研究,这些颗粒包含主要的基因组缺失,但通过测试携带病毒序列的瞬时转染质粒在感染细胞中的复制能力,仍保留其复制能力。到目前为止,尚无证据表明在苜蓿银纹夜蛾多核衣壳核型多角体病毒(AcMNPV)复制过程中这些假定的起点被实际利用。通过竞争性PCR进行起点定位的方法,我们获得了AcMNPV中HindIII-K区域和ie-1启动子序列的ori活性定量数据。我们还通过病毒感染的复制阶段,为病毒基因组背景下两个ori的差异活性提供了证据。在大小选择的新生DNA制剂中,比较代表HindIII-K和ie-1起点的分子数量与非ori的polH区域,结果显示在感染后期,HindIII-K ori的利用效率比ie-1区域高约14倍。在复制的早期和中期阶段,HindIII-K也是更活跃的ori。我们的结果提供了体内证据,支持AcMNPV复制涉及多个ori的观点,这些ori在病毒感染周期中以截然不同的效率被激活。