Séraphin B, Kandels-Lewis S
European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Cell. 1993 May 21;73(4):803-12. doi: 10.1016/0092-8674(93)90258-r.
The conserved nucleotides 9 and 10 of U1 small nuclear RNA (snRNA) have been proposed to base pair with either 5' exon or 3' splice site sequences. In S. pombe, U1 snRNA pairing with the conserved 3' splice site is required for the first step of splicing and viability. In contrast, we show that S. cerevisiae U1 mutants at positions 9 and 10 are fully functional. Splicing of several genes is normal in these strains, ruling out an essential base pairing between U1 snRNA and 3' splice sites. U1 snRNA positions 9 and 10 are shown to be involved in 5' splice site selection through their interaction with exon sequences. Our results demonstrate that some snRNA-pre-mRNA interactions are not evolutionarily conserved and that 3' splice site recognition occurs by different mechanisms in various organisms.
有人提出,U1小核RNA(snRNA)中保守的第9和第10个核苷酸会与5'外显子或3'剪接位点序列形成碱基对。在粟酒裂殖酵母中,U1 snRNA与保守的3'剪接位点配对是剪接第一步及细胞存活所必需的。相比之下,我们发现酿酒酵母中第9和第10位的U1突变体具有完全功能。在这些菌株中,几个基因的剪接正常,排除了U1 snRNA与3'剪接位点之间存在必需碱基对的可能性。研究表明,U1 snRNA的第9和第10位通过与外显子序列相互作用参与5'剪接位点的选择。我们的结果表明,一些snRNA与前体mRNA的相互作用在进化上并不保守,并且在不同生物体中,3'剪接位点的识别通过不同机制发生。