Self-splicing of the Tetrahymena group I ribozyme without conserved base-triples

被引:11
|
作者
Ikawa, Y [1 ]
Yoshioka, W [1 ]
Ohki, Y [1 ]
Shiraishi, H [1 ]
Inoue, T [1 ]
机构
[1] Kyoto Univ, Grad Sch Biostudies, Kyoto 6068502, Japan
关键词
D O I
10.1046/j.1365-2443.2001.00437.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Group I introns share a conserved core region consisting of two domains, P8-P3-P7 and P4-P6, joined by four base-triples. We showed previously that the T4 td intron can perform phosphoester transfer reactions at two splice sites in the absence of both P4-P6 and the conserved base-triples, whereas it is barely able to perform the intact splicing reaction due to the difficulty of conducting the sequential reactions. Results: Based on previous findings, we constructed a bimolecular ribozyme lacking a large portion of P4-P6 and the base-triples from the Tetrahymena intron, on the assumption that the long-range interactions of the peripheral regions in the two RNAs can compensate for the deteriorated core. The bimolecular ribozyme performed the intact splicing reaction. Conclusion: The present analysis indicates that the base-triples are nonessential, but that LA and the distal part of P4 in P4-P6 are important for conducting the splicing reaction. The reconstituted self-splicing ribozyme provides an amenable system for analysing the role(s) of elements in the core region in the self-splicing reaction mechanism.
引用
收藏
页码:411 / 420
页数:10
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