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Isolation of a transcriptive complex from Newcastle disease virions.

机译:从新城疫病毒粒子分离转录复合物。

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摘要

An active transcriptive complex was isolated from purified virions of Newcastle disease virus. After disruption with Triton X-100 and high salt, soluble and particulate fractions were separated by density gradient centrifugation. The transcriptive complex, recovered at a density of 1.275 g/cm3, appeared as a nucleocapsid structure by electron microscopy. When analyzed by polyacryl-amide gel electrophoresis, the nucleocapsids consisted of the nucleocapsid protein, a minor protein of 53,000 molecular weight, and the large L protein. Nucleocapsids possessed less than 1% of the hemagglutinating and neuraminidase activities originally associated with virions. The active complex synthesized predominantly 11 to 20S RNA in vitro and approximately one-fourth of the RNA molecules contained polyadenylic acid segments. In the presence of S-adenosyl-L-methionine, the RNA molecules were capped and methylated at the 5' termini. The transcriptive complex was also capable of methylating exogenous Escherichia coli RNA in the absence of viral RNA synthesis.
机译:从新城疫病毒的纯化病毒体中分离出活性转录复合物。用Triton X-100和高盐破坏后,通过密度梯度离心分离可溶和颗粒级分。以1.275 g / cm3的密度回收的转录复合物通过电子显微镜显示为核衣壳结构。当通过聚丙烯酰胺凝胶电泳分析时,核衣壳由核衣壳蛋白,分子量为53,000的次要蛋白和大L蛋白组成。核壳虫原本与病毒粒子相关的血凝和神经氨酸酶活性不到1%。该活性复合物主要在体外合成11至20S RNA,大约四分之一的RNA分子含有聚腺苷酸片段。在S-腺苷-L-蛋氨酸的存在下,将RNA分子加帽并在5'末端甲基化。在没有病毒RNA合成的情况下,转录复合物也能够甲基化外源大肠杆菌RNA。

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