Hooda-Dhingra U, Patel D D, Pickup D J, Condit R C
Department of Biochemistry, State University of New York, Buffalo 14214.
Virology. 1990 Jan;174(1):60-9. doi: 10.1016/0042-6822(90)90054-u.
We have used plasmid clones spanning the region encoding the 132-kDa subunit of the cowpox virus RNA polymerase (CPV rpo 132) to marker rescue each of five vaccinia virus (VV) temperature sensitive (ts) mutants, ts 27, ts 29, ts 32, ts 47, and ts 62, which together constitute a single complementation group. The experiments fine-map the vaccinia mutations to a 1.3-kb region containing the 3' end of the CPV rpo 132 gene. Phenotypic characterization shows that all five mutants are affected to varying extents in their ability to synthesize late viral proteins at the nonpermissive temperature, similar to other ts mutants with lesions in the 22- and the 147-kDa subunits of the VV RNA polymerase. Two mutants, ts 27 and ts 32, exhibit a delay in the synthesis of late viral proteins at both the permissive and the nonpermissive temperatures. We conclude that the five VV mutants affect the 132-kDa subunit of the VV RNA polymerase. Additional genetic experiments demonstrate intragenic complementation between ts 62 and three other members of this complementation group, ts 27, ts 29, and ts 32.
我们使用了跨越编码牛痘病毒RNA聚合酶132-kDa亚基(CPV rpo 132)区域的质粒克隆,对五个痘苗病毒(VV)温度敏感(ts)突变体ts 27、ts 29、ts 32、ts 47和ts 62进行标记拯救,这五个突变体共同构成一个单一的互补群。实验将痘苗病毒突变精确定位到一个1.3-kb的区域,该区域包含CPV rpo 132基因的3'端。表型特征表明,所有五个突变体在非允许温度下合成晚期病毒蛋白的能力都受到不同程度的影响,这与其他在VV RNA聚合酶22-kDa和147-kDa亚基中存在损伤的ts突变体类似。两个突变体ts 27和ts 32在允许温度和非允许温度下合成晚期病毒蛋白时均表现出延迟。我们得出结论,这五个VV突变体影响VV RNA聚合酶的132-kDa亚基。额外的遗传学实验证明了ts 62与该互补群的其他三个成员ts 27、ts 29和ts 32之间的基因内互补。