Oppenheim A, Sandalon Z, Peleg A, Shaul O, Nicolis S, Ottolenghi S
Department of Hematology, Hadassah University Hospital, Jerusalem, Israel.
J Virol. 1992 Sep;66(9):5320-8. doi: 10.1128/JVI.66.9.5320-5328.1992.
Encapsidation of simian virus 40 is a complex biological process involving DNA-protein and protein-protein interactions in the formation of a unique three-dimensional structure around the viral minichromosome. A pseudoviral system developed in our laboratory, in which the viral early and late gene products are supplied in trans (by helpers), was used to analyze the encapsidation process independent of viral gene expression. With this experimental system we have discovered a requirement for a specific DNA signal for encapsidation, ses (for simian virus 40 encapsidation signal).ses is present within a 200-bp DNA fragment, which includes, in addition to the viral origin of replication (ori), six GGGCGG repeats (GC boxes) and 26 bp of the enhancer element. Deletion of the GC boxes and the enhancer sequences almost abolished encapsidation, while DNA replication was only moderately decreased. The ability to encapsidate was not regained by reinserting a DNA fragment carrying ses in the sesdeleted plasmid 2 kbp away from the ori, suggesting that for encapsidation the two DNA elements have to be close to each other. These findings afford novel strategies for the investigation of viral encapsidation.
猴病毒40(Simian virus 40,SV40)的衣壳化是一个复杂的生物学过程,涉及在病毒微型染色体周围形成独特三维结构过程中的DNA-蛋白质和蛋白质-蛋白质相互作用。我们实验室开发了一种假病毒系统,其中病毒的早期和晚期基因产物通过反式(由辅助病毒)提供,用于分析独立于病毒基因表达的衣壳化过程。利用这个实验系统,我们发现了衣壳化对一种特定DNA信号的需求,即ses(猴病毒40衣壳化信号)。ses存在于一个200碱基对的DNA片段中,除了病毒复制起点(ori)外,该片段还包括六个GGGCGG重复序列(GC框)和26碱基对的增强子元件。删除GC框和增强子序列几乎消除了衣壳化,而DNA复制仅适度下降。将携带ses的DNA片段重新插入距ori 2千碱基对的ses缺失质粒中,衣壳化能力并未恢复,这表明对于衣壳化来说,这两个DNA元件必须彼此靠近。这些发现为病毒衣壳化的研究提供了新的策略。