Suppr超能文献

果蝇miR2诱导假多核糖体并抑制翻译起始。

Drosophila miR2 induces pseudo-polysomes and inhibits translation initiation.

作者信息

Thermann Rolf, Hentze Matthias W

机构信息

European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.

出版信息

Nature. 2007 Jun 14;447(7146):875-8. doi: 10.1038/nature05878. Epub 2007 May 16.

Abstract

MicroRNAs (miRs) inhibit protein synthesis by mechanisms that are as yet unresolved. We developed a cell-free system from Drosophila melanogaster embryos that faithfully recapitulates miR2-mediated translational control by means of the 3' untranslated region of the D. melanogaster reaper messenger RNA. Here we show that miR2 inhibits translation initiation without affecting mRNA stability. Surprisingly, miR2 induces the formation of dense (heavier than 80S) miRNPs ('pseudo-polysomes') even when polyribosome formation and 60S ribosomal subunit joining are blocked. An mRNA bearing an ApppG instead of an m7GpppG cap structure escapes the miR2-mediated translational block. These results directly show the inhibition of m7GpppG cap-mediated translation initiation as the mechanism of miR2 function, and uncover pseudo-polysomal messenger ribonucleoprotein assemblies that may help to explain earlier findings.

摘要

微小RNA(miRs)通过尚未明确的机制抑制蛋白质合成。我们利用黑腹果蝇胚胎开发了一种无细胞系统,该系统通过黑腹果蝇收割者信使核糖核酸的3'非翻译区忠实地重现了miR2介导的翻译控制。我们在此表明,miR2抑制翻译起始而不影响信使核糖核酸的稳定性。令人惊讶的是,即使多核糖体形成和60S核糖体亚基连接受阻,miR2也会诱导致密(比80S重)的微小核糖核蛋白颗粒(“假多核糖体”)形成。带有ApppG而非m7GpppG帽结构的信使核糖核酸可逃避miR2介导的翻译阻断。这些结果直接表明,m7GpppG帽介导的翻译起始抑制是miR2发挥功能的机制,并揭示了可能有助于解释早期研究结果的假多核糖体信使核糖核蛋白组装体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验