Sakai Yuta, Abe Koichi, Nakashima Saki, Yoshida Wataru, Ferri Stefano, Sode Koji, Ikebukuro Kazunori
Department of Biotechnology and Life Science, Graduate School of Engineering, Tokyo University of Agriculture and Technology , 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan.
ACS Synth Biol. 2014 Mar 21;3(3):152-62. doi: 10.1021/sb4000959. Epub 2013 Dec 18.
Noncoding small RNAs are involved in transcriptional and post-transcriptional gene regulation of target mRNAs by modulating mRNA elongation, stability, or translational efficiency. Many natural trans-encoded small RNAs contain a scaffold that allows binding of the RNA chaperone protein Hfq for conditional gene regulation. Here, we improved the gene regulation abilities of small RNAs by directly fusing the natural Escherichia coli trans-encoded small RNA-derived scaffolds, including Hfq-binding and rho-independent transcription terminator sequences, to the 3' end of the small RNAs that mediate RNA-based gene regulation. As target small RNAs to improve their gene regulation abilities, we selected small RNAs of artificial post-transcriptional riboregulators and transcriptional attenuators. Four different small RNA scaffolds were fused to the riboregulator and attenuator-derived small RNAs. Mutations were introduced into the best small RNA scaffold to improve its gene-regulation ability further. As a result, mutations predicted to stabilize the secondary structures of the small RNA scaffolds dramatically increased its ability to regulate gene expression of both the post-transcriptional riboregulator and transcriptional attenuator systems. We believe our engineered small RNA scaffolds are applicable to other RNA regulators for improving regulatory activity, and engineered small RNA scaffolds may present a valuable strategy to regulate target gene expression strongly.
非编码小RNA通过调节mRNA的延伸、稳定性或翻译效率参与靶mRNA的转录和转录后基因调控。许多天然反式编码小RNA含有一个支架,该支架允许RNA伴侣蛋白Hfq结合以进行条件性基因调控。在这里,我们通过将天然大肠杆菌反式编码小RNA衍生的支架(包括Hfq结合和不依赖rho的转录终止子序列)直接融合到介导基于RNA的基因调控的小RNA的3'末端,提高了小RNA的基因调控能力。作为提高其基因调控能力的靶小RNA,我们选择了人工转录后核糖调节因子和转录衰减子的小RNA。四种不同的小RNA支架被融合到核糖调节因子和衰减子衍生的小RNA上。对最佳小RNA支架引入突变以进一步提高其基因调控能力。结果,预测能稳定小RNA支架二级结构的突变显著提高了其调节转录后核糖调节因子和转录衰减子系统基因表达的能力。我们相信我们设计的小RNA支架适用于其他RNA调节因子以提高调节活性,并且设计的小RNA支架可能是一种有效调节靶基因表达的有价值策略。