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基于 RNase J 的 RNA 降解体在胃病原体幽门螺杆菌中是分隔的。

The RNase J-Based RNA Degradosome Is Compartmentalized in the Gastric Pathogen Helicobacter pylori.

机构信息

Institut Pasteur, Département de Microbiologie, Unité Pathogenèse de Helicobacter, UMR CNRS 2001, Paris, France.

Université de Paris, Sorbonne Paris Cité, Cellule Pasteur, Paris, France.

出版信息

mBio. 2020 Sep 15;11(5):e01173-20. doi: 10.1128/mBio.01173-20.

Abstract

Posttranscriptional regulation is a major level of gene expression control in any cell. In bacteria, multiprotein machines called RNA degradosomes are central for RNA processing and degradation, and some were reported to be compartmentalized inside these organelleless cells. The minimal RNA degradosome of the important gastric pathogen is composed of the essential ribonuclease RNase J and RhpA, its sole DEAD box RNA helicase, and plays a major role in the regulation of mRNA decay and adaptation to gastric colonization. Here, the subcellular localization of the RNA degradosome was investigated using cellular fractionation and both confocal and superresolution microscopy. We established that RNase J and RhpA are peripheral inner membrane proteins and that this association was mediated neither by ribosomes nor by RNA nor by the RNase Y membrane protein. In live cells, we observed that fluorescent RNase J and RhpA protein fusions assemble into nonpolar foci. We identified factors that regulate the formation of these foci without affecting the degradosome membrane association. Flotillin, a bacterial membrane scaffolding protein, and free RNA promote focus formation in Finally, RNase J-GFP (RNase J-green fluorescent protein) molecules and foci in cells were quantified by three-dimensional (3D) single-molecule fluorescence localization microscopy. The number and size of the RNase J foci were found to be scaled with growth phase and cell volume as previously reported for eukaryotic ribonucleoprotein granules. In conclusion, we propose that membrane compartmentalization and the regulated clustering of RNase J-based degradosome hubs represent important levels of control of their activity and specificity. is a bacterial pathogen that chronically colonizes the stomach of half of the human population worldwide. Infection by can lead to the development of gastric pathologies such as ulcers and adenocarcinoma, which causes up to 800,000 deaths in the world each year. Persistent colonization by relies on regulation of the expression of adaptation-related genes. One major level of such control is posttranscriptional regulation, which, in , largely relies on a multiprotein molecular machine, an RNA degradosome, that we previously discovered. In this study, we established that the two protein partners of this machine are associated with the membrane of Using cutting-edge microscopy, we showed that these complexes assemble into hubs whose formation is regulated by free RNA and scaled with bacterial size and growth phase. Organelleless cellular compartmentalization of molecular machines into hubs emerges as an important regulatory level in bacteria.

摘要

转录后调控是细胞中基因表达调控的主要水平。在细菌中,多蛋白机器称为 RNA 降解体,是 RNA 加工和降解的核心,据报道,其中一些在这些无细胞器的细胞内被分隔开。重要的胃病原体 的最小 RNA 降解体由必需的核糖核酸酶 RNase J 和 RhpA 组成,其唯一的 DEAD 盒 RNA 解旋酶,并在调节 mRNA 衰减和适应胃定植方面发挥主要作用。在这里,使用细胞分级分离和共焦和超分辨率显微镜研究了 RNA 降解体的亚细胞定位。我们确定 RNase J 和 RhpA 是外周内膜蛋白,这种关联既不是由核糖体介导的,也不是由 RNA 或 RNase Y 膜蛋白介导的。在活细胞中,我们观察到荧光 RNase J 和 RhpA 蛋白融合形成非极性焦点。我们确定了调节这些焦点形成而不影响降解体膜结合的因素。Flotillin 是一种细菌膜支架蛋白,游离 RNA 促进 中的焦点形成。最后,通过三维(3D)单分子荧光定位显微镜对细胞中 RNase J-GFP(RNase J-绿色荧光蛋白)分子和焦点进行定量。正如先前报道的真核核糖核蛋白颗粒一样,RNase J 焦点的数量和大小与生长阶段和细胞体积成正比。总之,我们提出膜分隔和基于 RNase J 的降解体枢纽的调节聚类代表了对其活性和特异性的重要控制水平。是一种慢性定植于全球一半人口胃部的细菌病原体。 感染 可导致胃溃疡和腺癌等胃部疾病的发展,每年在全球造成多达 80 万人死亡。 的持续定植依赖于与适应相关基因表达的调节。这种控制的主要水平之一是转录后调控,在 中,主要依赖于一种多蛋白分子机器,即我们之前发现的 RNA 降解体。在这项研究中,我们确定了该机器的两个蛋白质伴侣与 的膜相关联。使用最先进的显微镜技术,我们表明这些复合物组装成枢纽,其形成受游离 RNA 调节,并与细菌大小和生长阶段成正比。无细胞器的细菌细胞内分子机器的枢纽组装成为细菌中一个重要的调节水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d775/7492731/a836bb66d3b8/mBio.01173-20-f0001.jpg

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