Gracia Brant, Xue Yi, Bisaria Namita, Herschlag Daniel, Al-Hashimi Hashim M, Russell Rick
Department of Molecular Biosciences and the Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA.
Department of Biochemistry and Chemistry, Duke University Medical Center, Durham, NC 27710, USA.
J Mol Biol. 2016 Oct 9;428(20):3972-3985. doi: 10.1016/j.jmb.2016.07.013. Epub 2016 Jul 22.
Structured RNAs fold through multiple pathways, but we have little understanding of the molecular features that dictate folding pathways and determine rates along a given pathway. Here, we asked whether folding of a complex RNA can be understood from its structural modules. In a two-piece version of the Tetrahymena group I ribozyme, the separated P5abc subdomain folds to local native secondary and tertiary structure in a linked transition and assembles with the ribozyme core via three tertiary contacts: a kissing loop (P14), a metal core-receptor interaction, and a tetraloop-receptor interaction, the first two of which are expected to depend on native P5abc structure from the local transition. Native gel, NMR, and chemical footprinting experiments showed that mutations that destabilize the native P5abc structure slowed assembly up to 100-fold, indicating that P5abc folds first and then assembles with the core by conformational selection. However, rate decreases beyond 100-fold were not observed because an alternative pathway becomes dominant, with nonnative P5abc binding the core and then undergoing an induced-fit rearrangement. P14 is formed in the rate-limiting step along the conformational selection pathway but after the rate-limiting step along the induced-fit pathway. Strikingly, the assembly rate along the conformational selection pathway resembles that of an isolated kissing loop similar to P14, and the rate along the induced-fit pathway resembles that of an isolated tetraloop-receptor interaction. Our results indicate substantial modularity in RNA folding and assembly and suggest that these processes can be understood in terms of underlying structural modules.
结构化RNA通过多种途径折叠,但我们对决定折叠途径并确定沿给定途径折叠速率的分子特征了解甚少。在这里,我们探讨了是否可以从其结构模块来理解复杂RNA的折叠。在两件式的四膜虫I组核酶中,分离的P5abc亚结构域在一个连续的转变中折叠成局部天然二级和三级结构,并通过三个三级相互作用与核酶核心组装:一个吻式环(P14)、一个金属核心-受体相互作用和一个四环-受体相互作用,其中前两个预计依赖于局部转变产生的天然P5abc结构。天然凝胶、核磁共振和化学足迹实验表明,破坏天然P5abc结构稳定性的突变会使组装速度减慢多达100倍,这表明P5abc先折叠,然后通过构象选择与核心组装。然而,未观察到速率下降超过100倍,因为另一条途径占主导地位,即非天然的P5abc与核心结合,然后经历诱导契合重排。P14在构象选择途径的限速步骤中形成,但在诱导契合途径的限速步骤之后形成。引人注目的是,构象选择途径的组装速率类似于与P14相似的孤立吻式环的组装速率,而诱导契合途径的速率类似于孤立四环-受体相互作用的速率。我们的结果表明RNA折叠和组装具有显著的模块化,并表明这些过程可以根据潜在的结构模块来理解。