Roth Adam, Winkler Wade C, Regulski Elizabeth E, Lee Bobby W K, Lim Jinsoo, Jona Inbal, Barrick Jeffrey E, Ritwik Ankita, Kim Jane N, Welz Rüdiger, Iwata-Reuyl Dirk, Breaker Ronald R
Howard Hughes Medical Institute, USA.
Nat Struct Mol Biol. 2007 Apr;14(4):308-17. doi: 10.1038/nsmb1224. Epub 2007 Mar 25.
A previous bioinformatics-based search for riboswitches yielded several candidate motifs in eubacteria. One of these motifs commonly resides in the 5' untranslated regions of genes involved in the biosynthesis of queuosine (Q), a hypermodified nucleoside occupying the anticodon wobble position of certain transfer RNAs. Here we show that this structured RNA is part of a riboswitch selective for 7-aminomethyl-7-deazaguanine (preQ(1)), an intermediate in queuosine biosynthesis. Compared with other natural metabolite-binding RNAs, the preQ(1) aptamer appears to have a simple structure, consisting of a single stem-loop and a short tail sequence that together are formed from as few as 34 nucleotides. Despite its small size, this aptamer is highly selective for its cognate ligand in vitro and has an affinity for preQ(1) in the low nanomolar range. Relatively compact RNA structures can therefore serve effectively as metabolite receptors to regulate gene expression.
先前基于生物信息学对核糖开关的搜索在真细菌中产生了几个候选基序。这些基序之一通常位于参与queuosine(Q)生物合成的基因的5'非翻译区,Q是一种超修饰核苷,占据某些转移RNA反密码子摆动位置。在这里,我们表明这种结构化RNA是对7-氨基甲基-7-脱氮鸟嘌呤(preQ(1))具有选择性的核糖开关的一部分,preQ(1)是queuosine生物合成中的一种中间体。与其他天然代谢物结合RNA相比,preQ(1)适配体似乎具有简单的结构,由单个茎环和短尾序列组成,它们总共由少至34个核苷酸形成。尽管其尺寸较小,但该适配体在体外对其同源配体具有高度选择性,并且对preQ(1)具有低纳摩尔范围内的亲和力。因此,相对紧凑的RNA结构可以有效地作为代谢物受体来调节基因表达。