Heinrichs V, Bach M, Winkelmann G, Lührmann R
Institut fuer Molekularbiologie und Tumorforschung, Marburg, Federal Republic of Germany.
Science. 1990 Jan 5;247(4938):69-72. doi: 10.1126/science.2136774.
One of the functions of U1 small nuclear ribonucleoprotein (snRNP) in the splicing reaction of pre-mRNA molecules is the recognition of the 5' splice site. U1 snRNP proteins as well as base-pair interactions between U1 snRNA and the 5' splice site are important for the formation of the snRNP-pre-mRNA complex. To determine which proteins are needed for complex formation, the ability of U1 snRNPs gradually depleted of the U1-specific proteins C, A, and 70k to bind to an RNA molecule containing a 5' splice site sequence was studied in a nitrocellulose filter binding assay. The most significant effect was always observed when protein C was removed, either alone or together with other U1-specific proteins; the binding was reduced by 50 to 60%. Complementation of protein C-deficient U1 snRNPs with purified C protein restored their 5' splice site binding activity. These data suggest that protein C may potentiate the base-pair interaction between U1 RNA and the 5' splice site.
U1小核核糖核蛋白(snRNP)在pre - mRNA分子剪接反应中的功能之一是识别5'剪接位点。U1 snRNP蛋白以及U1 snRNA与5'剪接位点之间的碱基对相互作用对于snRNP - pre - mRNA复合物的形成很重要。为了确定复合物形成需要哪些蛋白质,在硝酸纤维素滤膜结合试验中研究了逐渐缺失U1特异性蛋白C、A和70k的U1 snRNP与含有5'剪接位点序列的RNA分子结合的能力。当单独去除蛋白C或与其他U1特异性蛋白一起去除时,总是观察到最显著的影响;结合减少了50%至60%。用纯化的C蛋白对缺乏蛋白C的U1 snRNP进行补充可恢复其5'剪接位点结合活性。这些数据表明蛋白C可能增强U1 RNA与5'剪接位点之间的碱基对相互作用。