Structural Insights Into Substrate Recognition by the Neurospora Varkud Satellite Ribozyme: Importance of U-Turns at the Kissing-Loop Junction

被引:16
作者
Bouchard, Patricia [1 ]
Legault, Pascale [1 ]
机构
[1] Univ Montreal, Dept Biochim & Med Mol, Montreal, PQ H3C 3J7, Canada
关键词
MAGNETIC-RESONANCE STRUCTURE; STEM-LOOP; SECONDARY-STRUCTURE; TRANSFER-RNA; METAL-BINDING; NMR STRUCTURE; PHOSPHATE GROUPS; MAGNESIUM-IONS; HYDROGEN-BONDS; CLEAVAGE;
D O I
10.1021/bi401491g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Substrate recognition by the Neurospora Varkud satellite ribozyme depends on the formation of a magnesium-dependent kissing-loop interaction between the stem-loop I (SLI) substrate and stem-loop V (SLV) of the catalytic domain. From mutagenesis studies, it has been established that this I/V kissing-loop interaction involves three Watson-Crick base pairs and is associated with a structural rearrangement of the SLI substrate that facilitates catalysis. Here, we report the NMR. structural characterization of this I/V kissing-loop using isolated stem-loops. NMR studies were performed on different SLI/SLV complexes containing a common SLV and shiftable, preshifted, or double-stranded SLI variants. These studies confirm the presence of three Watson-Crick base pairs at the kissing-loop junction and provide evidence for the structural rearrangement of shiftable SLI variants upon SLV binding. NMR structure determination of an SLI/SLV complex demonstrates that both the SLI and SLV loops adopt U-turn structures, which facilitates intermolecular Watson-Crick base pairing. Several other interactions at the I/V interface, including base triples and base stacking, help create a continuously stacked structure. These NMR studies provide a structural basis to understand the stability of the I/V kissing-loop interaction and lead us to propose a kinetic model for substrate activation in the VS ribozyme.
引用
收藏
页码:258 / 269
页数:12
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