Schu Daniel J, Zhang Aixia, Gottesman Susan, Storz Gisela
Laboratory of Molecular Biology, National Cancer Institute, Bethesda, MD, USA.
Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
EMBO J. 2015 Oct 14;34(20):2557-73. doi: 10.15252/embj.201591569. Epub 2015 Sep 15.
Many bacteria use small RNAs (sRNAs) and the RNA chaperone Hfq to regulate mRNA stability and translation. Hfq, a ring-shaped homohexamer, has multiple faces that can bind both sRNAs and their mRNA targets. We find that Hfq has at least two distinct ways in which it interacts with sRNAs; these different binding properties have strong effects on the stability of the sRNA in vivo and the sequence requirements of regulated mRNAs. Class I sRNAs depend on proximal and rim Hfq sites for stability and turn over rapidly. Class II sRNAs are more stable and depend on the proximal and distal Hfq sites for stabilization. Using deletions and chimeras, we find that while Class I sRNAs regulate mRNA targets with previously defined ARN repeats, Class II sRNAs regulate mRNAs carrying UA-rich rim-binding sites. We discuss how these different binding modes may correlate with different roles in the cell, with Class I sRNAs acting as emergency responders and Class II sRNAs acting as silencers.
许多细菌利用小RNA(sRNA)和RNA伴侣蛋白Hfq来调节mRNA的稳定性和翻译。Hfq是一种环状同型六聚体,有多个面,可同时结合sRNA及其mRNA靶标。我们发现Hfq与sRNA相互作用至少有两种不同方式;这些不同的结合特性对sRNA在体内的稳定性以及受调控mRNA的序列要求有很大影响。I类sRNA的稳定性依赖于近端和边缘Hfq位点,且周转迅速。II类sRNA更稳定,其稳定依赖于近端和远端Hfq位点。通过缺失和嵌合体实验,我们发现I类sRNA通过先前定义的ARN重复序列调节mRNA靶标,而II类sRNA则调节携带富含UA边缘结合位点的mRNA。我们讨论了这些不同的结合模式如何与细胞中的不同作用相关联,其中I类sRNA充当应急响应者而II类sRNA充当沉默子。