Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, England, UK.
Mol Cell. 2012 Sep 28;47(6):943-53. doi: 10.1016/j.molcel.2012.07.015. Epub 2012 Aug 16.
Numerous small non-coding RNAs (sRNAs) in bacteria modulate rates of translation initiation and degradation of target mRNAs, which they recognize through base-pairing facilitated by the RNA chaperone Hfq. Recent evidence indicates that the ternary complex of Hfq, sRNA and mRNA guides endoribonuclease RNase E to initiate turnover of both the RNAs. We show that a sRNA not only guides RNase E to a defined site in a target RNA, but also allosterically activates the enzyme by presenting a monophosphate group at the 5'-end of the cognate-pairing "seed." Moreover, in the absence of the target the 5'-monophosphate makes the sRNA seed region vulnerable to an attack by RNase E against which Hfq confers no protection. These results suggest that the chemical signature and pairing status of the sRNA seed region may help to both 'proofread' recognition and activate mRNA cleavage, as part of a dynamic process involving cooperation of RNA, Hfq and RNase E.
细菌中大量的小非编码 RNA(sRNA)通过 RNA 伴侣 Hfq 促进碱基配对来调节翻译起始和靶 mRNA 降解的速率,它们通过碱基配对来识别靶 mRNA。最近的证据表明,Hfq、sRNA 和 mRNA 的三元复合物指导内切核酸酶 RNase E 启动两种 RNA 的周转。我们表明,sRNA 不仅可以将 RNase E 引导到靶 RNA 中的特定位置,还可以通过在互补配对“种子”的 5'-端呈现单磷酸基团来变构激活酶。此外,在没有靶标的情况下,5'-单磷酸使 sRNA 种子区域易受 RNase E 的攻击,而 Hfq 对此没有提供保护。这些结果表明,sRNA 种子区域的化学特征和配对状态可能有助于“校对”识别并激活 mRNA 切割,这是一个涉及 RNA、Hfq 和 RNase E 合作的动态过程的一部分。