Department of Chemistry and Biochemistry, University of Colorado at Boulder, Boulder, Colorado 80309-0596, USA.
Nature. 2012 Dec 6;492(7427):133-7. doi: 10.1038/nature11607. Epub 2012 Oct 14.
Structures of riboswitch receptor domains bound to their effector have shown how messenger RNAs recognize diverse small molecules, but mechanistic details linking the structures to the regulation of gene expression remain elusive. To address this, here we solve crystal structures of two different classes of cobalamin (vitamin B(12))-binding riboswitches that include the structural switch of the downstream regulatory domain. These classes share a common cobalamin-binding core, but use distinct peripheral extensions to recognize different B(12) derivatives. In each case, recognition is accomplished through shape complementarity between the RNA and cobalamin, with relatively few hydrogen bonding interactions that typically govern RNA-small molecule recognition. We show that a composite cobalamin-RNA scaffold stabilizes an unusual long-range intramolecular kissing-loop interaction that controls mRNA expression. This is the first, to our knowledge, riboswitch crystal structure detailing how the receptor and regulatory domains communicate in a ligand-dependent fashion to regulate mRNA expression.
结合效应物的核糖开关受体结构域的结构展示了信使 RNA 如何识别各种小分子,但将结构与基因表达调控联系起来的机制细节仍难以捉摸。为了解决这个问题,我们在这里解决了两种不同类型的钴胺素(维生素 B(12))结合核糖开关的晶体结构,其中包括下游调节域的结构开关。这两类结构域共享一个共同的钴胺素结合核心,但使用不同的外围扩展来识别不同的 B(12)衍生物。在每种情况下,识别都是通过 RNA 和钴胺素之间的形状互补来完成的,与通常控制 RNA-小分子识别的氢键相互作用相对较少。我们表明,复合的钴胺素-RNA 支架稳定了一种不寻常的长程分子内亲吻环相互作用,这种相互作用控制着 mRNA 的表达。据我们所知,这是第一个详细描述受体和调节域如何以配体依赖的方式进行通信以调节 mRNA 表达的核糖开关晶体结构。