Ahn B Y, Gershon P D, Jones E V, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
Mol Cell Biol. 1990 Oct;10(10):5433-41. doi: 10.1128/mcb.10.10.5433-5441.1990.
Eucaryotic transcription factors that stimulate RNA polymerase II by increasing the efficiency of elongation of specifically or randomly initiated RNA chains have been isolated and characterized. We have identified a 30-kilodalton (kDa) vaccinia virus-encoded protein with apparent homology to SII, a 34-kDa mammalian transcriptional elongation factor. In addition to amino acid sequence similarities, both proteins contain C-terminal putative zinc finger domains. Identification of the gene, rpo30, encoding the vaccinia virus protein was achieved by using antibody to the purified viral RNA polymerase for immunoprecipitation of the in vitro translation products of in vivo-synthesized early mRNA selected by hybridization to cloned DNA fragments of the viral genome. Western immunoblot analysis using antiserum made to the vaccinia rpo30 protein expressed in bacteria indicated that the 30-kDa protein remains associated with highly purified viral RNA polymerase. Thus, the vaccinia virus protein, unlike its eucaryotic homolog, is an integral RNA polymerase subunit rather than a readily separable transcription factor. Further studies showed that the expression of rpo30 is regulated by dual early and later promoters.
通过提高特异性或随机起始的RNA链的延伸效率来刺激RNA聚合酶II的真核转录因子已被分离和鉴定。我们鉴定出一种30千道尔顿(kDa)的痘苗病毒编码蛋白,它与34 kDa的哺乳动物转录延伸因子SII具有明显的同源性。除了氨基酸序列相似性外,这两种蛋白都含有C末端假定的锌指结构域。通过使用针对纯化的病毒RNA聚合酶的抗体对通过与病毒基因组的克隆DNA片段杂交选择的体内合成早期mRNA的体外翻译产物进行免疫沉淀,实现了编码痘苗病毒蛋白的基因rpo30的鉴定。使用针对在细菌中表达的痘苗rpo30蛋白制备的抗血清进行的Western免疫印迹分析表明,30 kDa蛋白仍然与高度纯化的病毒RNA聚合酶相关联。因此,痘苗病毒蛋白与其真核同源物不同,它是RNA聚合酶的一个组成亚基,而不是一个易于分离的转录因子。进一步的研究表明,rpo30的表达受早期和晚期双重启动子调控。