Ahrens C H, Pearson M N, Rohrmann G F
Genetics Program, Oregon State University, Corvallis 97331-7301.
Virology. 1995 Mar 10;207(2):572-6. doi: 10.1006/viro.1995.1119.
A 7.5-kb region (96.8-2.5 m.u.), called Op5, of the Orgyia pseudotsugata multinucleocapsid nuclear polyhedrosis virus (OpMNPV) genome that contains an origin of DNA replication was characterized. This region replicates several times more efficiently and is unrelated to the previously identified putative origin of replication located on the viral HindIII-N fragment. In contrast to HindIII-N, the origin on Op5 contains repeated sequences with limited sequence identity to the homologous regions from AcMNPV. In isolation, these repeated sequences were not sufficient for origin activity in OpMNPV-infected Lymantria dispar cells, but required an additional 1.3 kb of sequences located to the left of the repeats. Four regions of the OpMNPV genome that crosshybridize with the repeated region were also found to replicate in our infection-dependent DNA replication assay. A deletion clone of Op5 that replicates efficiently in OpMNPV-infected L. dispar cells, was found to replicate at less than 2% the replication level of AcMNPV hr2 in AcMNPV-infected Spodoptera frugiperda cells.
对云杉芽卷叶蛾多核衣壳核型多角体病毒(OpMNPV)基因组中一个7.5kb的区域(96.8 - 2.5 m.u.)进行了表征,该区域称为Op5,包含一个DNA复制起点。该区域的复制效率比之前鉴定的位于病毒HindIII - N片段上的假定复制起点高出数倍,且与后者无关。与HindIII - N不同,Op5上的起点包含一些重复序列,这些重复序列与苜蓿银纹夜蛾核型多角体病毒(AcMNPV)同源区域的序列一致性有限。单独来看,这些重复序列在OpMNPV感染的舞毒蛾细胞中不足以发挥起点活性,而是需要位于重复序列左侧的额外1.3kb序列。在我们依赖感染的DNA复制试验中,还发现OpMNPV基因组中与该重复区域交叉杂交的四个区域也能复制。在OpMNPV感染的舞毒蛾细胞中高效复制的Op5缺失克隆,在苜蓿银纹夜蛾核型多角体病毒感染的草地贪夜蛾细胞中的复制水平不到苜蓿银纹夜蛾核型多角体病毒hr2的2%。