Ahn B Y, Gershon P D, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1994 Mar 11;269(10):7552-7.
The association of a 94,000-Da viral polypeptide, called Rap94, with 30-40% of the multisubunit DNA-dependent RNA polymerase molecules purified from infectious vaccinia virus particles was established by immunoaffinity chromatography. The submolar amount of Rap94, relative to RNA polymerase, was confirmed by quantitative immunoblotting of total virion extracts. Only the RNA polymerase molecules containing Rap94 could functionally interact with VETF, the vaccinia virus early transcription factor, to transcribe a double-stranded DNA template regulated by a viral early stage promoter. Rap94 was required for the synthesis of short oligoribonucleotides and for the formation of stable ternary transcription complexes. With a nonspecific single-stranded DNA template, however, the Rap94-deficient polymerase had greater catalytic activity than the Rap94-containing polymerase. These data support a model in which Rap94 confers specificity to the RNA polymerase for promoters of early stage genes.
通过免疫亲和层析法确定,一种名为Rap94的94,000道尔顿病毒多肽与从感染性痘苗病毒颗粒中纯化的30%-40%的多亚基依赖DNA的RNA聚合酶分子相关联。相对于RNA聚合酶,Rap94的亚摩尔量通过对总病毒粒子提取物的定量免疫印迹得到证实。只有含有Rap94的RNA聚合酶分子才能与痘苗病毒早期转录因子VETF发生功能相互作用,以转录由病毒早期启动子调控的双链DNA模板。Rap94是合成短寡核糖核苷酸和形成稳定三元转录复合物所必需的。然而,对于非特异性单链DNA模板,缺乏Rap94的聚合酶比含有Rap94的聚合酶具有更高的催化活性。这些数据支持了一个模型,即Rap94赋予RNA聚合酶对早期基因启动子的特异性。