Department of Biochemistry, Stanford University, Stanford, California 94305, USA.
J Am Chem Soc. 2012 Feb 1;134(4):1910-3. doi: 10.1021/ja2083575. Epub 2012 Jan 17.
We have investigated the role of a single-stranded RNA junction, J1/2, that connects the substrate-containing P1 duplex to the remainder of the Tetrahymena group I ribozyme. Single-turnover kinetics, fluorescence anisotropy, and single-molecule fluorescence resonance energy transfer studies of a series of J1/2 mutants were used to probe the sequence dependence of the catalytic activity, the P1 dynamics, and the thermodynamics of docking of the P1 duplex into the ribozyme's catalytic core. We found that A29, the center A of three adenosine residues in J1/2, contributes 2 orders of magnitude to the overall ribozyme activity, and double-mutant cycles suggested that J1/2 stabilizes the docked state of P1 over the undocked state via a tertiary interaction involving A29 and the first base pair in helix P2 of the ribozyme, A31·U56. Comparative sequence analysis of this group I intron subclass suggests that the A29 interaction sets one end of a molecular ruler whose other end specifies the 5'-splice site and that this molecular ruler is conserved among a subclass of group I introns related to the Tetrahymena intron. Our results reveal substantial functional effects from a seemingly simple single-stranded RNA junction and suggest that junction sequences may evolve rapidly to provide important interactions in functional RNAs.
我们研究了连接含有底物的 P1 双链体和 Tetrahymena 组 I 核酶其余部分的单链 RNA 连接点 J1/2 的作用。使用一系列 J1/2 突变体的单轮动力学、荧光各向异性和单分子荧光共振能量转移研究来探测催化活性、P1 动力学以及 P1 双链体对接入核酶催化核心的热力学的序列依赖性。我们发现,J1/2 中的三个腺苷残基中心 A29 对整体核酶活性有 2 个数量级的贡献,双突变循环表明,J1/2 通过涉及 A29 和核酶的 P2 螺旋的第一个碱基对 A31·U56 的三级相互作用稳定 P1 的对接状态而不是非对接状态。对该组 I 内含子亚类的比较序列分析表明,A29 相互作用设定了分子标尺的一端,其另一端指定 5'-剪接位点,并且该分子标尺在与 Tetrahymena 内含子相关的一组 I 内含子中是保守的。我们的结果揭示了看似简单的单链 RNA 连接点的显著功能影响,并表明连接点序列可能会快速进化,以在功能性 RNA 中提供重要的相互作用。