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能够合成42S和26S新生RNA链的Semliki森林病毒复制复合体。

Semliki Forest virus replication complex capable of synthesizing 42S and 26S nascent RNA chains.

作者信息

Gomatos P J, Kääriäinen L, Keränen S, Ranki M, Sawicki D L

出版信息

J Gen Virol. 1980 Jul;49(1):61-9. doi: 10.1099/0022-1317-49-1-61.

Abstract

A complex synthesizing Semliki Forest virus (SFV)-specific RNAs was purified from infected HeLa cells. During purification, the RNA-synthesizing complex was monitored by the presence of RNA chains synthesized during a 1 min pulse in vivo and the ability to synthesize 42S and 26S RNAs in vitro. Finally, the protein composition of the replication complex was analysed. Thirty to 40% of the pulse-labelled RNAs and 10 to 25% of the polymerase activity present in the postnuclear supernatant were recovered in smooth membranes. At this stage of purification single stranded 42S and 26S RNA were synthesized and released from the replication complex in vitro. After treatment of the smooth membrane fraction with Triton X-100 the replication complex was solubilized. When analysed by sucrose gradient centrifugation, the solubilized replication complex distributed heterogeneously. It had reduced RNA polymerase activity, but was still able to synthesize both 42S and 26S nascent RNA chains which were not released from RIs and RFs. The non-structural protein ns70 was the major virus-specified component associated with the replication complex.

摘要

从感染的HeLa细胞中纯化出一种复杂的合成塞姆利基森林病毒(SFV)特异性RNA。在纯化过程中,通过体内1分钟脉冲期间合成的RNA链的存在以及体外合成42S和26S RNA的能力来监测RNA合成复合物。最后,分析了复制复合物的蛋白质组成。核后上清液中30%至40%的脉冲标记RNA和10%至25%的聚合酶活性在光滑膜中回收。在纯化的这个阶段,单链42S和26S RNA在体外合成并从复制复合物中释放。用Triton X-100处理光滑膜部分后,复制复合物被溶解。通过蔗糖梯度离心分析时,溶解的复制复合物分布不均一。它的RNA聚合酶活性降低,但仍能够合成未从RIs和RFs释放的42S和26S新生RNA链。非结构蛋白ns70是与复制复合物相关的主要病毒特异性成分。

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