RNA Group, Department of Biochemistry, University of Sherbrooke, Sherbrooke, Quebec J1H 5N4, Canada.
Genes Dev. 2012 Apr 1;26(7):726-39. doi: 10.1101/gad.182493.111.
The RNA chaperone Hfq is mostly known to help small regulatory RNAs (sRNAs) interact with target mRNAs to block initiating ribosomes. In this model, whereas the sRNA is directly competing with initiating 30S ribosomal subunits, Hfq plays only an indirect role, allowing optimal sRNA-mRNA pairing. Here we report that Hfq is recruited by a sRNA, Spot42, to bind to a precise AU-rich region in the vicinity of the translation initiation region (TIR) of sdhC mRNA and competes directly with 30S ribosomal subunits. We show that the sRNA Spot42 binds sdhC too far upstream of the TIR to directly repress translation initiation in vitro and in vivo. Contrary to the canonical model of sRNA regulation, this suggests a new mechanism where Hfq is directly involved in the translational repression of the target mRNA and where the sRNA acts only as a recruitment factor.
RNA 伴侣蛋白 Hfq 主要帮助小分子调控 RNA(sRNA)与靶 mRNA 相互作用,从而阻止起始核糖体的形成。在该模型中,虽然 sRNA 直接与起始的 30S 核糖体亚基竞争,但 Hfq 仅发挥间接作用,从而实现 sRNA-mRNA 配对的最优化。在这里,我们报告说 Hfq 被 sRNA Spot42 募集,以结合 sdhC mRNA 翻译起始区(TIR)附近的一个精确的 AU 富含区域,并直接与 30S 核糖体亚基竞争。我们发现 sRNA Spot42 在 TIR 上游结合 sdhC 的位置太远,以至于无法直接在体外和体内抑制翻译起始。与 sRNA 调控的典型模型相反,这表明了一种新的机制,其中 Hfq 直接参与靶 mRNA 的翻译抑制,而 sRNA 仅作为招募因子发挥作用。