Black E P, Moussatche N, Condit R C
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville 32610, USA.
Virology. 1998 Jun 5;245(2):313-22. doi: 10.1006/viro.1998.9166.
Prior genetic analysis suggests that there may exist an interaction between the products of the vaccinia virus genes A18R, a putative negative transcription elongation factor, and G2R, a putative positive transcription elongation factor. In addition, affinity purification of polyhistidine-tagged G2R protein overexpressed in vaccinia virus-infected cells, reported here, results in copurification of the vaccinia H5R protein, previously characterized as a late viral transcription factor. We have therefore used several methods to screen further for interactions among the G2R, A18R, and H5R proteins. Methods include copurification or co-immunoprecipitation of proteins overexpressed during vaccinia virus infection, activation of the gal 4 promoter by gal 4 fusions in the yeast two-hybrid system, and co-immunoprecipitation of proteins synthesized in vitro in a rabbit reticulocyte lysate. The results reveal interactions which include all possible pairwise combinations of the three proteins G2R, A18R, and H5R; however, not all possible permutations of the interactions are observed and the interactions are not observed in all environments tested. The results suggest that the vaccinia virus proteins G2R, A18R, and H5R interact as part of a higher order transcription complex.
先前的基因分析表明,痘苗病毒基因A18R(一种假定的负转录延伸因子)和G2R(一种假定的正转录延伸因子)的产物之间可能存在相互作用。此外,本文报道的在痘苗病毒感染细胞中过表达的多聚组氨酸标记的G2R蛋白的亲和纯化,导致了痘苗H5R蛋白的共纯化,H5R蛋白先前被鉴定为一种晚期病毒转录因子。因此,我们使用了几种方法来进一步筛选G2R、A18R和H5R蛋白之间的相互作用。方法包括痘苗病毒感染期间过表达蛋白的共纯化或共免疫沉淀、酵母双杂交系统中gal 4融合对gal 4启动子的激活,以及兔网织红细胞裂解物中体外合成蛋白的共免疫沉淀。结果揭示了相互作用,其中包括G2R、A18R和H5R这三种蛋白的所有可能的两两组合;然而,并非观察到所有可能的相互作用排列,并且在所有测试环境中均未观察到这些相互作用。结果表明,痘苗病毒蛋白G2R、A18R和H5R作为更高阶转录复合物的一部分相互作用。