Parvin J D, Palese P, Honda A, Ishihama A, Krystal M
Department of Microbiology, Mount Sinai School of Medicine, New York, New York 10029.
J Virol. 1989 Dec;63(12):5142-52. doi: 10.1128/JVI.63.12.5142-5152.1989.
Influenza virus polymerase, which was prepared depleted of viral RNA, was used to copy small RNA templates prepared from plasmid-encoded sequences. Template constructions containing only the 3' end of genomic RNA were shown to be efficiently copied, indicating that the promoter lay solely within the 15-nucleotide 3' terminus. Sequences not specific for the influenza virus termini were not copied, and, surprisingly, RNAs containing termini identical to those from plus-sense cRNA were copied at low levels. The specificity for recognition of the virus sense promoter was further defined by site-specific mutagenesis. It was also found that increased levels of viral protein were required in order to catalyze both the cap endonuclease-primed and primer-free RNA synthesis from these model templates, as well as from genomic-length RNAs. This finding indicates that the reconstituted system has catalytic properties very similar to those of native viral ribonucleoprotein complexes.
制备的不含病毒RNA的流感病毒聚合酶用于复制从质粒编码序列制备的小RNA模板。仅包含基因组RNA 3'末端的模板构建体显示能有效复制,这表明启动子仅位于15个核苷酸的3'末端内。非流感病毒末端特异性的序列未被复制,令人惊讶的是,含有与正链cRNA末端相同末端的RNA复制水平很低。通过位点特异性诱变进一步确定了对病毒正义启动子识别的特异性。还发现,为了催化从这些模型模板以及基因组长度RNA进行帽状核酸内切酶引发的和无引物的RNA合成,需要增加病毒蛋白的水平。这一发现表明,重组系统具有与天然病毒核糖核蛋白复合物非常相似的催化特性。