Williamson C L, Desai N M, Burke J M
Department of Microbiology, University of Vermont, Burlington 05405.
Nucleic Acids Res. 1989 Jan 25;17(2):675-89. doi: 10.1093/nar/17.2.675.
Compensatory mutations have been constructed which demonstrate that P8 and P6, two of nine proposed base-pairing interactions characteristic of group I introns, exist within the folded structure of the Tetrahymena thermophila rRNA intervening sequence, and that these secondary structure elements are important for splicing in E. coli and self-splicing in vitro. Two-base mutations in the 5' and 3' segments of P8 are predicted to disrupt P8 and a strong splicing-defective phenotype is observed in each case. A compensatory four-base mutation in P8 is predicted to restore pairing, and results in the restoration of splicing activity to nearly wild type levels. Thus, we conclude that P8 exists and is essential for splicing. In contrast to the strong phenotypes generally exhibited by mutations which disrupt RNA secondary structure, a two-base mutation in L8, the loop between P8[5'] and P8[3'], results in only a slight decrease in splicing activity. We also tested P6, a pairing which is proposed to consist of only two base-pairs in this intron. A two-base mutation in P6[3'] reduces splicing activity to a greater extent than does a two-base mutation in P6[5']. Comparison of the activities of these mutants and a compensatory P6 four-base mutant support the existence of P6, and suggest that the P6 pairing may be particularly important in the exon ligation step of splicing.
已构建了补偿性突变,结果表明,嗜热四膜虫rRNA间隔序列折叠结构中存在P8和P6,这是I组内含子九个拟碱基配对相互作用中的两个,并且这些二级结构元件对于在大肠杆菌中剪接和体外自我剪接很重要。预计P8的5'和3'区段中的双碱基突变会破坏P8,并且在每种情况下均观察到强烈的剪接缺陷表型。预计P8中的补偿性四碱基突变可恢复配对,并导致剪接活性恢复到接近野生型水平。因此,我们得出结论,P8存在且对于剪接至关重要。与破坏RNA二级结构的突变通常表现出的强烈表型相反,L8(P8[5']和P8[3']之间的环)中的双碱基突变仅导致剪接活性略有下降。我们还测试了P6,该配对在此内含子中仅由两个碱基对组成。P6[3']中的双碱基突变比P6[5']中的双碱基突变更大程度地降低了剪接活性。这些突变体与补偿性P6四碱基突变体活性的比较支持P6的存在,并表明P6配对在剪接的外显子连接步骤中可能特别重要。