Levis R, Weiss B G, Tsiang M, Huang H, Schlesinger S
Cell. 1986 Jan 17;44(1):137-45. doi: 10.1016/0092-8674(86)90492-7.
Defective-interfering (DI) genomes of a virus contain sequence information essential for their replication and packaging. They need not contain any coding information and therefore are a valuable tool for identifying cis-acting, regulatory sequences in a viral genome. To identify these sequences in a DI genome of Sindbis virus, we cloned a cDNA copy of a complete DI genome directly downstream of the promoter for the SP6 bacteriophage DNA dependent RNA polymerase. The cDNA was transcribed into RNA, which was transfected into chicken embryo fibroblasts in the presence of helper Sindbis virus. After one to two passages the DI RNA became the major viral RNA species in infected cells. Data from a series of deletions covering the entire DI genome show that only sequences in the 162 nucleotide region at the 5' terminus and in the 19 nucleotide region at the 3' terminus are specifically required for replication and packaging of these genomes.
病毒的缺陷干扰(DI)基因组包含其复制和包装所必需的序列信息。它们无需包含任何编码信息,因此是鉴定病毒基因组中顺式作用调控序列的宝贵工具。为了在辛德毕斯病毒的DI基因组中鉴定这些序列,我们将完整DI基因组的cDNA拷贝直接克隆到SP6噬菌体DNA依赖性RNA聚合酶启动子的下游。该cDNA被转录成RNA,在辅助性辛德毕斯病毒存在的情况下将其转染到鸡胚成纤维细胞中。经过一到两代传代后,DI RNA成为感染细胞中主要的病毒RNA种类。一系列覆盖整个DI基因组的缺失数据表明,这些基因组的复制和包装特别需要5'末端162个核苷酸区域和3'末端19个核苷酸区域中的序列。