Amegadzie B Y, Ahn B Y, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1991 Jul 25;266(21):13712-8.
The gene rpo35, encoding a subunit of the vaccinia virus DNA-dependent RNA polymerase, was identified, and its RNA and protein products were characterized. An Mr 35,000 polypeptide, which bound antibody to the purified RNA polymerase, was synthesized in reticulocyte lysates programmed with viral mRNA that hybridized to a 2,300-base pair segment of the viral genome. Determination of the sequence of the DNA segment revealed four potential protein coding regions, none of which had evident similarity to any described RNA polymerase subunit of prokaryotes or eukaryotes. One open reading frame that could encode a 35,400-Da protein was identified as rpo35 on the basis of mRNA hybridization, cell-free translation, and immunoprecipitation. The identification was confirmed by sequencing tryptic peptides of the authentic Mr 35,000 RNA polymerase subunit. Antiserum to the purified recombinant protein, expressed in bacteria, reacted specifically with a Mr 35,000 polypeptide that was detected starting 2 h after virus infection and that co-sedimented with RNA polymerase purified from virions. RNA analyses indicated that the 5'-end of an early transcript started 25 nucleotides upstream of rpo35, which is consistent with the location of an early promoter consensus sequence.
鉴定出编码痘苗病毒DNA依赖性RNA聚合酶一个亚基的rpo35基因,并对其RNA和蛋白质产物进行了表征。在用与病毒基因组2300碱基对片段杂交的病毒mRNA编程的网织红细胞裂解物中,合成了一种与纯化的RNA聚合酶抗体结合的35000 Mr多肽。对该DNA片段序列的测定揭示了四个潜在的蛋白质编码区,其中没有一个与任何已描述的原核生物或真核生物RNA聚合酶亚基有明显的相似性。基于mRNA杂交、无细胞翻译和免疫沉淀,一个可编码35400 Da蛋白质的开放阅读框被鉴定为rpo35。通过对真实的35000 Mr RNA聚合酶亚基的胰蛋白酶肽段测序,证实了该鉴定。针对在细菌中表达的纯化重组蛋白的抗血清,与一种35000 Mr多肽特异性反应,该多肽在病毒感染后2小时开始被检测到,并与从病毒粒子中纯化的RNA聚合酶共沉淀。RNA分析表明,一个早期转录本的5′端起始于rpo35上游25个核苷酸处,这与一个早期启动子共有序列的位置一致。