Morrow C D, Warren B, Lentz M R
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6050-4. doi: 10.1073/pnas.84.17.6050.
The poliovirus genome is replicated by a virus-encoded RNA-dependent RNA polymerase (RNA polymerase). The RNA polymerase is first synthesized as a larger precursor polypeptide, which is subsequently processed by a viral proteinase, 3Cpro, to give the mature polymerase molecule, 3Dpol. To further characterize the poliovirus RNA polymerase, we have constructed plasmids that expressed this protein in Escherichia coli. The plasmids consisted of fusions between the E. coli DNA encoding the first 13 amino acids of the trp operon leader protein and viral genes encoding the 3Cpro and 3Dpol polypeptides. E. coli harboring such plasmids gave significant, inducible levels of enzymatically active RNA polymerase as determined by the poly(A).oligo(U) poly(U) polymerase assay. The purified RNA polymerase activity from E. coli corresponded to a protein with the approximate molecular weight of the mature 3Dpol protein. The availability of a recombinant, enzymatically active poliovirus RNA polymerase provides a system in which we can precisely delineate the role this enzyme plays in the regulation of poliovirus replication.
脊髓灰质炎病毒基因组由病毒编码的RNA依赖性RNA聚合酶(RNA聚合酶)进行复制。RNA聚合酶最初作为一种较大的前体多肽合成,随后由病毒蛋白酶3Cpro进行加工,从而产生成熟的聚合酶分子3Dpol。为了进一步表征脊髓灰质炎病毒RNA聚合酶,我们构建了在大肠杆菌中表达这种蛋白质的质粒。这些质粒由编码色氨酸操纵子前导蛋白前13个氨基酸的大肠杆菌DNA与编码3Cpro和3Dpol多肽的病毒基因之间的融合体组成。通过聚(A)·寡聚(U)聚(U)聚合酶测定法确定,携带此类质粒的大肠杆菌产生了显著的、可诱导水平的具有酶活性的RNA聚合酶。从大肠杆菌中纯化的RNA聚合酶活性对应于一种分子量与成熟3Dpol蛋白近似的蛋白质。重组的、具有酶活性的脊髓灰质炎病毒RNA聚合酶的可得性提供了一个系统,在这个系统中我们可以精确描述这种酶在脊髓灰质炎病毒复制调控中所起的作用。