Vos J C, Sasker M, Stunnenberg H G
European Molecular Biology Laboratory, Gene Expression Program, Heidelberg, FRG.
EMBO J. 1991 Sep;10(9):2553-8. doi: 10.1002/j.1460-2075.1991.tb07795.x.
It has previously been demonstrated that vaccinia virus capping enzyme is involved both in the formation of a 5' cap structure and in termination of early transcription. Here we show that capping enzyme has an additional activity which is required for transcription of intermediate genes. VITF-A and VITF-B have been defined as two activities which together with RNA polymerase are necessary and sufficient to transcribe intermediate genes in vitro. VITF-A and the viral capping enzyme are shown to copurify to near homogeneity. Direct evidence that capping enzyme is VITF-A was obtained by complementation of a reconstituted transcription system with viral capping enzyme expressed in Escherichia coli. Although capping enzyme is a cofactor in early transcription termination, intermediate transcription is not terminated in response to the early termination signal. Capping enzyme is shown to form a complex with RNA polymerase in the absence of VITF-B. This appears to be a prerequisite for the formation of a stable initiation complex.
先前已经证明,痘苗病毒加帽酶参与5'帽结构的形成以及早期转录的终止。在此我们表明,加帽酶具有中间基因转录所需的额外活性。VITF-A和VITF-B已被定义为两种活性,它们与RNA聚合酶一起在体外转录中间基因时是必需且充分的。VITF-A和病毒加帽酶被证明可共纯化至近乎均一。通过用在大肠杆菌中表达的病毒加帽酶补充重组转录系统,获得了加帽酶就是VITF-A的直接证据。尽管加帽酶是早期转录终止的辅助因子,但中间转录不会响应早期终止信号而终止。在没有VITF-B的情况下,加帽酶被证明可与RNA聚合酶形成复合物。这似乎是形成稳定起始复合物的先决条件。