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一种小的酵母RNA可选择性抑制脊髓灰质炎病毒RNA编程的翻译内部起始:与结合病毒5'非翻译区的细胞蛋白的特异性相互作用。

A small yeast RNA selectively inhibits internal initiation of translation programmed by poliovirus RNA: specific interaction with cellular proteins that bind to the viral 5'-untranslated region.

作者信息

Das S, Coward P, Dasgupta A

机构信息

Department of Microbiology and Immunology, UCLA School of Medicine 90024-1747.

出版信息

J Virol. 1994 Nov;68(11):7200-11. doi: 10.1128/JVI.68.11.7200-7211.1994.

Abstract

We have purified, sequenced, and prepared a synthetic clone of a small (60-nucleotide) RNA molecule from the yeast Saccharomyces cerevisiae that had previously been isolated on the basis of its ability to selectively block the translation of poliovirus mRNA. RNA derived from the clone by transcription with T7 RNA polymerase appears to block translation initiation by internal ribosome entry (cap independent) but does not significantly affect cap-dependent translation. Deletion analysis of the poliovirus 5'-untranslated region (5'-UTR) has shown that yeast inhibitor RNA (I-RNA) requires internal ribosome entry site sequences to inhibit the translation of poliovirus RNA in vitro. Using a bicistronic RNA construct, we show that I-RNA preferentially inhibits translation by internal ribosome entry. Gel retardation and UV cross-linking studies demonstrate that I-RNA specifically binds proteins which interact with RNA secondary structures within the poliovirus 5'-UTR presumably involved in internal initiation. Specifically, purified I-RNA competes with virus RNA structures within the 5'-UTR which bind a cellular protein with an approximate molecular mass of 52 kDa. Finally, when transfected into HeLa cells, I-RNA efficiently inhibits the replication of poliovirus RNA presumably by inhibiting translation of the input virus RNA.

摘要

我们已经从酿酒酵母中纯化、测序并制备了一个小(60个核苷酸)RNA分子的合成克隆,该分子先前是基于其选择性阻断脊髓灰质炎病毒mRNA翻译的能力而分离出来的。通过用T7 RNA聚合酶转录从该克隆获得的RNA似乎通过内部核糖体进入(不依赖帽结构)来阻断翻译起始,但对依赖帽结构的翻译没有显著影响。对脊髓灰质炎病毒5'-非翻译区(5'-UTR)的缺失分析表明,酵母抑制RNA(I-RNA)在体外抑制脊髓灰质炎病毒RNA翻译需要内部核糖体进入位点序列。使用双顺反子RNA构建体,我们表明I-RNA优先通过内部核糖体进入来抑制翻译。凝胶阻滞和紫外线交联研究表明,I-RNA特异性结合与脊髓灰质炎病毒5'-UTR内可能参与内部起始的RNA二级结构相互作用的蛋白质。具体而言,纯化的I-RNA与5'-UTR内与一种分子量约为52 kDa的细胞蛋白结合的病毒RNA结构竞争。最后,当转染到HeLa细胞中时,I-RNA可能通过抑制输入病毒RNA的翻译有效地抑制脊髓灰质炎病毒RNA的复制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/237159/88f4a11eeeac/jvirol00020-0391-a.jpg

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