Jarrell K A, Dietrich R C, Perlman P S
Department of Molecular Genetics, Ohio State University, Columbus 43210-1292.
Mol Cell Biol. 1988 Jun;8(6):2361-6. doi: 10.1128/mcb.8.6.2361-2366.1988.
A self-splicing group II intron of yeast mitochondrial DNA (aI5g) was divided within intron domain 4 to yield two RNAs that trans-spliced in vitro with associated trans-branching of excised intron fragments. Reformation of the domain 4 secondary structure was not necessary for the trans reaction, since domain 4 sequences were shown to be dispensable. Instead, the trans reaction depended on a previously unpredicted interaction between intron domain 5, the most highly conserved region of group II introns, and another region of the RNA. Domain 5 was shown to be essential for cleavage at the 5' splice site. It stimulated that cleavage when supplied as a trans-acting RNA containing only 42 nucleotides of intron sequence. The relevance of our findings to in vivo trans-splicing mechanisms is discussed.
酵母线粒体DNA的一个自我剪接II类内含子(aI5g)在内含子结构域4内被分割,产生了两个RNA,它们在体外进行反式剪接,并伴随着切除的内含子片段的反式分支。结构域4二级结构的重新形成对于反式反应不是必需的,因为已证明结构域4序列是可有可无的。相反,反式反应依赖于II类内含子中最保守的区域——内含子结构域5与RNA的另一个区域之间以前未预测到的相互作用。已表明结构域5对于5'剪接位点的切割至关重要。当作为仅包含42个核苷酸内含子序列的反式作用RNA提供时,它会刺激这种切割。我们讨论了我们的发现与体内反式剪接机制的相关性。