Zhang D, Rosbash M
Department of Biology, Howard Hughes Medical Institute, Brandeis University, Waltham, Massachusetts 02454, USA.
Genes Dev. 1999 Mar 1;13(5):581-92. doi: 10.1101/gad.13.5.581.
In the yeast commitment complex and the mammalian E complex, there is an important base-pairing interaction between the 5' end of U1 snRNA and the conserved 5' splice site region of pre-mRNA. But no protein contacts between splicing proteins and the pre-mRNA substrate have been defined in or near this region of early splicing complexes. To address this issue, we used 4-thiouridine-substituted 5' splice site-containing RNAs as substrates and identified eight cross-linked proteins, all of which were identified previously as commitment complex components. The proteins were localized to three domains: the exon, the six nucleotides of the 5' ss region, and the downstream intron. The results indicate that the 5' splice site region and environs are dense with protein contacts in the commitment complex and suggest that some of them make important contributions to formation or stability of the U1 snRNP-pre-mRNA complex.
在酵母前体mRNA剪接起始复合物和哺乳动物E复合物中,U1小核RNA的5'端与前体mRNA保守的5'剪接位点区域之间存在重要的碱基配对相互作用。但在早期剪接复合物的该区域内或其附近,尚未明确剪接蛋白与前体mRNA底物之间存在蛋白质接触。为解决这一问题,我们使用含4-硫尿苷取代的5'剪接位点的RNA作为底物,鉴定出8种交联蛋白,所有这些蛋白先前均被鉴定为剪接起始复合物的组分。这些蛋白定位于三个结构域:外显子、5'剪接位点区域的六个核苷酸以及下游内含子。结果表明,在剪接起始复合物中,5'剪接位点区域及其周围存在密集的蛋白质接触,这表明其中一些接触对U1小核核糖核蛋白-前体mRNA复合物的形成或稳定性有重要贡献。