Ryan K W
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101-0318.
J Virol Methods. 1992 Jan;36(1):85-90. doi: 10.1016/0166-0934(92)90159-b.
Vaccinia virus-dependent CAT expression was observed in virus-infected cells cotransfected with a promoterless CAT gene. Restriction endonuclease resection of the CAT plasmid indicated that expression was due to recognition by vaccinia virus RNA polymerase of sequences within the CAT gene itself, probably located within the 5' untranslated region of the gene. This observation is relevant to the design of reverse-genetic systems which use CAT as a reporter gene to detect replication of negative-strand RNA virus pseudogenomes.
在用无启动子的氯霉素乙酰转移酶(CAT)基因共转染的病毒感染细胞中观察到了依赖痘苗病毒的CAT表达。对CAT质粒进行限制性内切酶切割表明,表达是由于痘苗病毒RNA聚合酶识别了CAT基因本身内部的序列,这些序列可能位于该基因的5'非翻译区内。这一观察结果与反向遗传系统的设计相关,该系统使用CAT作为报告基因来检测负链RNA病毒假基因组的复制。