Westhof E
Institut de Biologie Moléculaire et Cellulaire du CNRS, 15 rue R. Descartes, F-67084 Strasbourg, France.
Biochem Soc Trans. 2002 Nov;30(Pt 6):1149-52. doi: 10.1042/bst0301149.
Before the discovery of catalytic RNA, tRNA molecules were the most studied RNA molecules for understanding RNA folding. Afterwards, group I introns, because of their stability and the fact that structural folding could be monitored by following their catalytic activity, became the molecule of choice for studying RNA architecture and folding. A major advantage of group I introns for studying the catalytic activity of RNA molecules is that catalytic activity is triggered by the addition of external guanosine cofactors. The self-splicing activity can therefore be precisely controlled. Using group I introns, several RNA motifs central to RNA-RNA self-assembly and folding were discovered. The analysis of the recent X-ray structures of the rRNA subunits indicates that several motifs present in the ribosome occur also in various group I introns.
在催化性RNA被发现之前,转运RNA(tRNA)分子是为了解RNA折叠而研究得最多的RNA分子。此后,I组内含子因其稳定性以及可通过跟踪其催化活性来监测结构折叠这一事实,成为研究RNA结构和折叠的首选分子。I组内含子在研究RNA分子催化活性方面的一个主要优势是,催化活性由外部鸟苷辅因子的添加触发。因此,自我剪接活性可以得到精确控制。利用I组内含子,发现了几个对RNA - RNA自我组装和折叠至关重要的RNA基序。对核糖体RNA亚基最近的X射线结构分析表明,核糖体中存在的几个基序也出现在各种I组内含子中。