Dimastrogiovanni Daniela, Fröhlich Kathrin S, Bandyra Katarzyna J, Bruce Heather A, Hohensee Susann, Vogel Jörg, Luisi Ben F
Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Department of Molecular Biology, Princeton University, Princeton, United States.
Elife. 2014 Dec 31;3:e05375. doi: 10.7554/eLife.05375.
Bacterial small RNAs (sRNAs) are key elements of regulatory networks that modulate gene expression. The sRNA RydC of Salmonella sp. and Escherichia coli is an example of this class of riboregulators. Like many other sRNAs, RydC bears a 'seed' region that recognises specific transcripts through base-pairing, and its activities are facilitated by the RNA chaperone Hfq. The crystal structure of RydC in complex with E. coli Hfq at a 3.48 Å resolution illuminates how the protein interacts with and presents the sRNA for target recognition. Consolidating the protein-RNA complex is a host of distributed interactions mediated by the natively unstructured termini of Hfq. Based on the structure and other data, we propose a model for a dynamic effector complex comprising Hfq, small RNA, and the cognate mRNA target.
细菌小RNA(sRNA)是调节基因表达的调控网络的关键元件。沙门氏菌属和大肠杆菌的sRNA RydC就是这类核糖调节因子的一个例子。与许多其他sRNA一样,RydC带有一个通过碱基配对识别特定转录本的“种子”区域,其活性由RNA伴侣蛋白Hfq促进。RydC与大肠杆菌Hfq复合物的晶体结构以3.48 Å的分辨率揭示了该蛋白如何与sRNA相互作用并将其呈递给靶标识别。巩固蛋白质-RNA复合物的是由Hfq天然无结构的末端介导的一系列分散相互作用。基于该结构和其他数据,我们提出了一个由Hfq、小RNA和同源mRNA靶标组成的动态效应复合物模型。