首页> 美国卫生研究院文献>Journal of Virology >Semliki Forest Virus-Specific RNAs Synthesized In Vitro by Enzyme from Infected BHK Cells
【2h】

Semliki Forest Virus-Specific RNAs Synthesized In Vitro by Enzyme from Infected BHK Cells

机译:通过感染的BHK细胞的酶体外合成Semliki森林病毒特异性RNA

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

When Semliki Forest virus (SFV)-infected BHK cells were disrupted 4 h after infection, 75 to 90% of the total virus-specific RNA synthesizing enzyme was found in the large particle fraction, along with 75 to 90% of the in vivo-synthesized double-stranded RNAs. The RNA products of this enzyme-template complex in an in vitro system were double-stranded RNAs sedimenting predominantly at 18S, and single-stranded RNAs sedimenting at 42S, 26S, and 22S. The various virus-specific SFV RNAs synthesized in vitro were associated with different sized structures, and thus each was separable by differential centrifugation. Kinetic and pulse-chase experiments showed that the double-stranded RNAs were the precursors to the single-stranded RNAs. There were several double-stranded RNAs identified both in the in vitro product and also in extracts from infected cells. The major replicative form had a molecular weight of 4.4 × 106.
机译:当感染Semliki Forest病毒(SFV)的BHK细胞在感染后4小时被破坏时,在大颗粒级分中发现了病毒特异性RNA合成酶总数的75%至90%,以及体内75-90%合成的双链RNA。在体外系统中,这种酶-模板复合物的RNA产物主要是在18S沉淀的双链RNA和在42S,26S和22S沉淀的单链RNA。体外合成的各种病毒特异性SFV RNA具有不同大小的结构,因此可以通过差速离心进行分离。动力学和脉冲追踪实验表明,双链RNA是单链RNA的前体。在体外产物以及感染细胞的提取物中都鉴定出了几种双链RNA。主要复制形式的分子量为4.4×10 6

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号