The RNA-chaperone Hfq catalyses the annealing of bacterial small RNAs (sRNAs) with target mRNAs to regulate gene expression in response to environmental stimuli. Hfq acts on a diverse set of sRNA-mRNA pairs using a variety of different molecular mechanisms. Here, we present an unusual crystal structure showing two Hfq-RNA complexes interacting via their bound RNA molecules. The structure contains two Hfq(6):A(18) RNA assemblies positioned face-to-face, with the RNA molecules turned towards each other and connected via interdigitating base stacking interactions at the center. Biochemical data further confirm the observed interaction, and indicate that RNA-mediated contacts occur between Hfq-RNA complexes with various (ARN)(X) motif containing RNA sequences in vitro, including the stress response regulator OxyS and its target, fhlA. A systematic computational survey also shows that phylogenetically conserved (ARN)(X) motifs are present in a subset of sRNAs, some of which share similar modular architectures. We hypothesise that Hfq can co-opt RNA-RNA base stacking, an unanticipated structural trick, to promote the interaction of (ARN)(X) motif containing sRNAs with target mRNAs on a "speed-dating" fashion, thereby supporting their regulatory function.
Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq.
在 RNA 伴侣蛋白 Hfq 的晶体结构中,分子间碱基堆积介导 RNA-RNA 相互作用
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作者:Schulz Eike C, Seiler Markus, Zuliani Cecilia, Voigt Franka, Rybin Vladimir, Pogenberg Vivian, Mücke Norbert, Wilmanns Matthias, Gibson Toby J, Barabas Orsolya
| 期刊: | Scientific Reports | 影响因子: | 3.900 |
| 时间: | 2017 | 起止号: | 2017 Aug 29; 7(1):9903 |
| doi: | 10.1038/s41598-017-10085-8 | 研究方向: | 免疫/内分泌 |
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