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原核生物的Argonaute蛋白——RNA干扰主题的变体

Prokaryotic Argonautes - variations on the RNA interference theme.

作者信息

van der Oost John, Swarts Daan C, Jore Matthijs M

机构信息

Laboratory of Microbiology, Wageningen University, Dreijenplein 10, 6703 HB Wageningen, Netherlands.

Laboratory of Microbiology, Wageningen University, Dreijenplein 10, 6703 HB Wageningen, Netherlands. ; Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Microb Cell. 2014 Apr 15;1(5):158-159. doi: 10.15698/mic2014.05.144.

Abstract

The discovery of RNA interference (RNAi) has been a major scientific breakthrough. This RNA-guided RNA interference system plays a crucial role in a wide range of regulatory and defense mechanisms in eukaryotes. The key enzyme of the RNAi system is Argonaute (Ago), an endo-ribonuclease that uses a small RNA guide molecule to specifically target a complementary RNA transcript. Two functional classes of eukaryotic Ago have been described: catalytically active Ago that cleaves RNA targets complementary to its guide, and inactive Ago that uses its guide to bind target RNA to down-regulate translation efficiency. A recent comparative genomics study has revealed that Argonaute-like proteins are also encoded by prokaryotic genomes. Interestingly, there is a lot of variation among these prokaryotic Argonaute (pAgo) proteins with respect to domain architecture: some resemble the eukaryotic Ago (long pAgo) containing a complete or disrupted catalytic site, while others are truncated versions (short pAgo) that generally contain an incomplete catalytic site. Prokaryotic Agos with an incomplete catalytic site often co-occur with (predicted) nucleases. Based on this diversity, and on the fact that homologs of other RNAi-related protein components (such as Dicer nucleases) have never been identified in prokaryotes, it has been predicted that variations on the eukaryotic RNAi theme may occur in prokaryotes.

摘要

RNA干扰(RNAi)的发现是一项重大的科学突破。这种由RNA引导的RNA干扰系统在真核生物的广泛调控和防御机制中发挥着关键作用。RNAi系统的关键酶是Argonaute(Ago),它是一种内切核糖核酸酶,利用小RNA引导分子特异性靶向互补的RNA转录本。真核生物的Ago已被描述为两种功能类别:具有催化活性的Ago,可切割与其引导序列互补的RNA靶标;以及无活性的Ago,它利用其引导序列结合靶标RNA以下调翻译效率。最近的一项比较基因组学研究表明,原核生物基因组也编码了类似Argonaute的蛋白质。有趣的是,这些原核生物Argonaute(pAgo)蛋白在结构域结构方面存在很大差异:一些类似于真核生物的Ago(长pAgo),含有完整或破坏的催化位点,而另一些是截短版本(短pAgo),通常含有不完整的催化位点。催化位点不完整的原核生物Ago通常与(预测的)核酸酶共同出现。基于这种多样性,以及在原核生物中从未鉴定出其他RNAi相关蛋白成分(如Dicer核酸酶)的同源物这一事实,有人预测原核生物中可能会出现真核生物RNAi主题的变体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b8/5354601/66f4a7af2145/mic-01-158-g01.jpg

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