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核质穿梭的 ARGONAUTE1 提示植物 microRNA 途径的修正模型。

Nucleo-cytosolic Shuttling of ARGONAUTE1 Prompts a Revised Model of the Plant MicroRNA Pathway.

机构信息

Department of Biology, Swiss Federal Institute of Technology (ETH), Universitätstrasse 2, Zürich 8092, Switzerland.

Institute of Bioengineering, School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne 1015, Switzerland; Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland.

出版信息

Mol Cell. 2018 Feb 15;69(4):709-719.e5. doi: 10.1016/j.molcel.2018.01.007. Epub 2018 Feb 1.

Abstract

Unlike in metazoans, plant microRNAs (miRNAs) undergo stepwise nuclear maturation before engaging cytosolic, sequence-complementary transcripts in association with the silencing effector protein ARGONAUTE1 (AGO1). Since their discovery, how and under which form plant miRNAs translocate to the cytosol has remained unclear, as has their sub-cellular AGO1 loading site(s). Here, we show that the N termini of all plant AGO1s contain a nuclear-localization (NLS) and nuclear-export signal (NES) that, in Arabidopsis thaliana (At), enables AtAGO1 nucleo-cytosolic shuttling in a Leptomycin-B-inhibited manner, diagnostic of CRM1(EXPO1)/NES-dependent nuclear export. Nuclear-only AtAGO1 contains the same 2'O-methylated miRNA cohorts as its nucleo-cytosolic counterpart, but it preferentially interacts with the miRNA loading chaperone HSP90. Furthermore, mature miRNA translocation and miRNA-mediated silencing both require AtAGO1 nucleo-cytosolic shuttling. These findings lead us to propose a substantially revised view of the plant miRNA pathway in which miRNAs are matured, methylated, loaded into AGO1 in the nucleus, and exported to the cytosol as AGO1:miRNA complexes in a CRM1(EXPO1)/NES-dependent manner.

摘要

与后生动物不同,植物 microRNAs (miRNAs) 在与沉默效应蛋白 ARGONAUTE1 (AGO1) 结合之前,经历分步核成熟,然后与胞质中的序列互补转录本结合。自发现以来,植物 miRNAs 如何以及以何种形式转移到细胞质中,以及它们的亚细胞 AGO1 加载部位仍然不清楚。在这里,我们表明所有植物 AGO1 的 N 端都包含一个核定位 (NLS) 和核输出信号 (NES),在拟南芥 (At) 中,这使得 AtAGO1 以 Leptomycin-B 抑制的方式核质穿梭,这是 CRM1(EXPO1)/NES 依赖性核输出的诊断标志。仅在核内的 AtAGO1 含有与其核质对应物相同的 2'O-甲基化 miRNA 群体,但它优先与 miRNA 加载伴侣 HSP90 相互作用。此外,成熟 miRNA 的转运和 miRNA 介导的沉默都需要 AtAGO1 的核质穿梭。这些发现使我们提出了一个对植物 miRNA 途径的实质性修正观点,即在细胞核中成熟、甲基化、加载到 AGO1 中,并以 CRM1(EXPO1)/NES 依赖性方式作为 AGO1:miRNA 复合物输出到细胞质中。

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