Lafontaine D A, Norman D G, Lilley D M
CRC Nucleic Acid Structure Research Group, Department of Biochemistry, The University of Dundee, Dundee DD1 4HN, UK.
EMBO J. 2001 Mar 15;20(6):1415-24. doi: 10.1093/emboj/20.6.1415.
The VS nucleolytic ribozyme has a core comprising five helices organized by two three-way junctions. The ribozyme can act in trans on a hairpin-loop substrate, with which it interacts via tertiary contacts. We have determined that one of the junctions (2-3-6) undergoes two-stage ion-dependent folding into a stable conformation, and have determined the global structure of the folded junction using long-range distance restraints derived from fluorescence resonance energy transfer. A number of sequence variants in the junction are severely impaired in ribozyme cleavage, and there is good correlation between changes in activity and alteration in the folding of junction 2-3-6. These studies point to a special importance of G and A nucleotides immediately adjacent to helix II, and comparison with a similar junction of known structure indicates that this could adopt a guanine-wedge structure. We propose that the 2-3-6 junction organizes important aspects of the structure of the ribozyme to facilitate productive association with the substrate, and suggest that this results in an interaction between the substrate and the A730 loop to create the active complex.
VS 核酶解核酶具有一个核心,该核心由两个三向连接点组织的五个螺旋组成。该核酶可以对发夹环底物进行反式作用,并通过三级接触与之相互作用。我们已经确定其中一个连接点(2-3-6)经历两阶段离子依赖性折叠形成稳定构象,并使用源自荧光共振能量转移的长程距离限制确定了折叠连接点的整体结构。连接点中的许多序列变体在核酶切割中严重受损,并且活性变化与连接点2-3-6折叠变化之间存在良好的相关性。这些研究表明紧邻螺旋II的G和A核苷酸具有特殊重要性,与已知结构的类似连接点进行比较表明这可能采用鸟嘌呤楔形结构。我们提出2-3-6连接点组织了核酶结构的重要方面,以促进与底物的有效结合,并表明这导致底物与A730环之间的相互作用以形成活性复合物。