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一种痘苗病毒晚期转录因子与一种结合病毒晚期启动子的因子共纯化,并被未感染的HeLa细胞提取物互补。

A vaccinia virus late transcription factor copurifies with a factor that binds to a viral late promoter and is complemented by extracts from uninfected HeLa cells.

作者信息

Wright C F, Hubbs A E, Gunasinghe S K, Oswald B W

机构信息

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston 29425, USA.

出版信息

J Virol. 1998 Feb;72(2):1446-51. doi: 10.1128/JVI.72.2.1446-1451.1998.

Abstract

We have previously described a vaccinia virus late transcription factor, VLTF-X, which we found to be present in cells at early and late times in infection. In this study, transcription complementation assays were used to demonstrate that VLTF-X activity is also present in virion extracts and in the cytoplasm of uninfected HeLa cells. Mobility shift assays performed on various VLTF-X preparations revealed that a late promoter DNA-binding activity cochromatographed and cosedimented with VLTF-X activity. Competition experiments demonstrated that this binding was specific for the late promoter region of the probe and that late transcription was dramatically reduced by an oligonucleotide that blocked factor-DNA complex formation but was only minimally affected by an oligonucleotide that did not inhibit complex formation. These results suggest that a cellular factor may participate in vaccinia virus late transcription. These findings also confirm the requirement for VLTF-X and distinguish it from any of the previously described vaccinia virus late transcription factors, which have all been mapped to the viral genome. Finally, these studies also suggest that the biochemical role for VLTF-X may be in late promoter recognition.

摘要

我们之前描述过一种痘苗病毒晚期转录因子VLTF-X,我们发现它在感染的早期和晚期均存在于细胞中。在本研究中,采用转录互补试验来证明VLTF-X活性也存在于病毒粒子提取物和未感染的HeLa细胞的细胞质中。对各种VLTF-X制剂进行的迁移率变动分析显示,一种晚期启动子DNA结合活性与VLTF-X活性共层析且共沉降。竞争实验表明,这种结合对探针的晚期启动子区域具有特异性,并且晚期转录会因一种阻断因子-DNA复合物形成的寡核苷酸而显著降低,但仅受到不抑制复合物形成的寡核苷酸的轻微影响。这些结果表明,一种细胞因子可能参与痘苗病毒晚期转录。这些发现还证实了对VLTF-X的需求,并将其与之前描述的所有已定位到病毒基因组的痘苗病毒晚期转录因子区分开来。最后,这些研究还表明,VLTF-X的生化作用可能在于晚期启动子识别。

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