Identification of structural elements critical for inter-domain interactions in a group II self-splicing intron

被引:38
作者
Jestin, JL [1 ]
Deme, E [1 ]
Jacquier, A [1 ]
机构
[1] INST PASTEUR, DEPT BIOTECHNOL, CNRS URA 13CO, ARN, LAB METAB, F-75724 PARIS 15, FRANCE
关键词
catalytic RNA; group II introns; modification interference; ribozyme; RNA structure;
D O I
10.1093/emboj/16.10.2945
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
Thus far, conventional biophysical techniques, such as NMR spectroscopy or X-ray crystallography, allow the determination, at atomic resolution, of only structural domains of large RNA molecules such as group I introns, Determination of their overall spatial organization thus still relies on modeling. This requires that a relatively high number of tertiary interactions are defined in order to get sufficient topological constraints, Here, we report the use of a modification interference assay to identify structural elements involved in interdomain interactions. We used this technique, in a group II intron, to identify the elements involved in the interactions between domain V and the rest of the molecule, Domain V contains many of the active site components of these ribozymes, In addition to a previously identified II nucleotide motif involved in the binding of the domain V terminal GAAA tetraloop, a small number of elements were shown to be essential for domain V binding. In particular, we show that domain III is specifically required for the interaction with sequences encompassing the conserved 2 nucleotide bulge of domain V.
引用
收藏
页码:2945 / 2954
页数:10
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