Chanfreau G, Legrain P, Dujon B, Jacquier A
Département de Biologie Moléculaire, Institut Pasteur, Paris, France.
Nucleic Acids Res. 1994 Jun 11;22(11):1981-7. doi: 10.1093/nar/22.11.1981.
The splicing of group II and nuclear pre-mRNAs introns occurs via a similar splicing pathway and some of the RNA-RNA interactions involved in these splicing reactions show structural similarities. Recently, genetic analyses performed in a group II intron and the yeast nuclear actin gene suggested that non Watson-Crick interactions between intron boundaries are important for the second splicing step efficiency in both classes of introns. We here show that, in the yeast nuclear rp51A intron, a G to A mutation at the first position activates cryptic 3' splice sites with the sequences UAC/ or UAA/. Moreover, the natural 3' splice site could be reactivated by a G to C substitution of the last intron nucleotide. These results demonstrate that the interaction between the first and last intron nucleotides is a conserved feature of nuclear pre-mRNA splicing in yeast and is involved in the mechanism of 3' splice site selection.
II类内含子和细胞核前体mRNA内含子的剪接通过相似的剪接途径发生,并且这些剪接反应中涉及的一些RNA-RNA相互作用表现出结构上的相似性。最近,在一个II类内含子和酵母细胞核肌动蛋白基因中进行的遗传分析表明,内含子边界之间的非沃森-克里克相互作用对于这两类内含子的第二步剪接效率都很重要。我们在此表明,在酵母细胞核rp51A内含子中,第一位的G到A突变会激活具有UAC/或UAA/序列的隐蔽3'剪接位点。此外,天然的3'剪接位点可以通过最后一个内含子核苷酸的G到C替换而重新激活。这些结果表明,第一个和最后一个内含子核苷酸之间的相互作用是酵母细胞核前体mRNA剪接的一个保守特征,并且参与3'剪接位点选择的机制。