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流感病毒粒子RNA体外复制模板的合成。

Synthesis of the templates for influenza virion RNA replication in vitro.

作者信息

Beaton A R, Krug R M

出版信息

Proc Natl Acad Sci U S A. 1984 Aug;81(15):4682-6. doi: 10.1073/pnas.81.15.4682.

Abstract

To elucidate the mechanism(s) of influenza viral RNA replication, we have developed an in vitro system in which the templates for viral RNA replication as well as the viral messenger RNAs (mRNAs) are synthesized. Because the synthesis of both the viral mRNAs and the template RNAs occurs in the nucleus of infected cells, we determined whether infected cell nuclei are active in the synthesis of these two types of transcripts in vitro. Nuclei isolated as early as 1-2 hr after infection catalyze the in vitro synthesis of both the viral mRNAs and template RNAs. The time course of appearance of these activities indicates that they most likely represent the transcriptional complexes functioning in vivo. Template RNA synthesis catalyzed by the nuclei in vitro is independent of concomitant protein synthesis; rather, it utilizes preformed proteins present in the nuclear preparations. This protein pool can be depleted by treating the infected cells with a protein synthesis inhibitor prior to the isolation of the nuclei, thereby rendering the nuclei inactive in template RNA synthesis in vitro. This activity can be restored by the addition of infected cell cytoplasmic extracts or of the high-speed supernatant fraction from these extracts. These results indicate that the cytoplasmic fraction from infected cells enables the viral transcription complex to continue transcription past the site at which termination occurs during viral mRNA synthesis and also suggest that this fraction enables the transcription complex to initiate transcription without the capped primer used in viral mRNA synthesis.

摘要

为阐明流感病毒RNA复制的机制,我们开发了一种体外系统,其中病毒RNA复制的模板以及病毒信使RNA(mRNA)得以合成。由于病毒mRNA和模板RNA的合成均发生在受感染细胞的细胞核中,我们确定了受感染的细胞核在体外合成这两种转录本时是否具有活性。早在感染后1 - 2小时分离得到的细胞核能够催化病毒mRNA和模板RNA的体外合成。这些活性出现的时间进程表明,它们很可能代表了在体内发挥作用的转录复合物。细胞核在体外催化的模板RNA合成不依赖于同时进行的蛋白质合成;相反,它利用核制剂中预先存在的蛋白质。通过在分离细胞核之前用蛋白质合成抑制剂处理受感染细胞,可以耗尽这个蛋白质库,从而使细胞核在体外模板RNA合成中失去活性。通过添加受感染细胞的细胞质提取物或这些提取物的高速上清液部分,可以恢复这种活性。这些结果表明,受感染细胞的细胞质部分能够使病毒转录复合物在病毒mRNA合成过程中越过终止位点继续转录,并且还表明该部分能够使转录复合物在没有病毒mRNA合成中使用的带帽引物的情况下启动转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11aa/391554/4ff96affbe67/pnas00616-0074-a.jpg

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