Newman A, Norman C
MRC Laboratory of Molecular Biology, Cambridge, England.
Cell. 1991 Apr 5;65(1):115-23. doi: 10.1016/0092-8674(91)90413-s.
Recognition of 5' splice sites in pre-mRNA splicing is achieved in part by base pairing with U1 snRNA. We have used interactive suppression in the yeast Saccharomyces cerevisiae to look for other factors involved in 5' splice-site recognition. This approach identified an extragenic suppressor that activates a cryptic 5' splice site. The suppressor is a gene for U5 snRNA (snR7) with a single base mutation in a strictly conserved 9 base sequence. This suggests that U5 snRNA can play a part in determining the position of 5' splice-site cleavage. Consistent with this, we have been able to isolate other mutations in the 9 base element in U5 snRNA that specifically activate a second cryptic 5' splice site nearby.
前体mRNA剪接过程中对5'剪接位点的识别部分是通过与U1 snRNA碱基配对来实现的。我们利用酿酒酵母中的交互抑制来寻找参与5'剪接位点识别的其他因子。这种方法鉴定出一个激活隐蔽5'剪接位点的基因外抑制子。该抑制子是一个U5 snRNA(snR7)基因,在一段严格保守的9碱基序列中有一个单碱基突变。这表明U5 snRNA可能在确定5'剪接位点切割位置中发挥作用。与此一致的是,我们已经能够在U5 snRNA的9碱基元件中分离出其他突变,这些突变特异性地激活附近的第二个隐蔽5'剪接位点。