Séraphin B, Rosbash M
Institut Curie-Biologie, Campus Universitaire, Orsay, France.
EMBO J. 1991 May;10(5):1209-16. doi: 10.1002/j.1460-2075.1991.tb08062.x.
Commitment complexes contain U1 snRNP as well as pre-mRNA and are the earliest functional complexes that have been described during in vitro spliceosome assembly. We have used a gel retardation assay to analyze the role of the yeast pre-mRNA cis-acting sequences in commitment complex formation. The results suggest that only a proper 5' splice site sequence is required for efficient U1 snRNA-pre-mRNA complex formation. A role for the highly conserved UACUAAC branchpoint sequence is indicated, however, by competition experiments and by the direct analysis of branchpoint mutant substrates, which cannot form one of the two commitment complex species observed with wild-type substrates. The results suggest that the formation of a U1 snRNP-pre-mRNA complex is not dependent upon the presence of a branchpoint sequence but that the branchpoint sequence is recognized prior to U2 snRNP addition during in vitro spliceosome assembly.
起始复合物包含U1 snRNP以及前体mRNA,是体外剪接体组装过程中最早被描述的功能复合物。我们利用凝胶阻滞试验来分析酵母前体mRNA顺式作用序列在起始复合物形成中的作用。结果表明,高效形成U1 snRNA - 前体mRNA复合物仅需要合适的5'剪接位点序列。然而,竞争实验以及对分支点突变底物的直接分析表明,高度保守的UACUAAC分支点序列具有作用,分支点突变底物无法形成野生型底物所观察到的两种起始复合物中的一种。结果表明,U1 snRNP - 前体mRNA复合物的形成不依赖于分支点序列的存在,但在体外剪接体组装过程中,在添加U2 snRNP之前分支点序列就被识别。