Caliguiri L A, Compans R W
J Virol. 1974 Aug;14(2):191-7. doi: 10.1128/JVI.14.2.191-197.1974.
The products synthesized in vitro by an RNA-dependent RNA polymerase isolated from influenza virus-infected BHK21-F cells were analyzed by velocity sedimentation, annealing techniques, and acrylamide-agarose gel electrophoresis. Approximately 50% of the RNA synthesized in vitro remains associated with the 50 to 70S ribonucleoprotein complex containing polymerase activity; the remainder of the RNA polymerase product sediments heterogeneously with a peak at 13S. At least 90% of the in vitro product hybridizes with virion RNA. If polypeptides are labeled early in the growth cycle, both the P and NP polypeptides are detected in the ribonucleoprotein complex by acrylamide gel electrophoresis. The results suggest that the polypeptide composition and the products of the cell-associated RNA polymerase are similar to those of the RNA transcriptase associated with influenza virus particles.
通过从感染流感病毒的BHK21 - F细胞中分离出的RNA依赖性RNA聚合酶在体外合成的产物,采用速度沉降、退火技术和丙烯酰胺 - 琼脂糖凝胶电泳进行分析。体外合成的RNA中约50%仍与含有聚合酶活性的50至70S核糖核蛋白复合物相关;RNA聚合酶产物的其余部分沉降不均一,峰值在13S。体外产物中至少90%与病毒粒子RNA杂交。如果在生长周期早期对多肽进行标记,通过丙烯酰胺凝胶电泳可在核糖核蛋白复合物中检测到P和NP多肽。结果表明,与细胞相关的RNA聚合酶的多肽组成和产物与与流感病毒粒子相关的RNA转录酶相似。