Liao X C, Tang J, Rosbash M
Howard Hughes Medical Institute, Department of Biology, Brandeis University, Waltham, Massachusetts 02254.
Genes Dev. 1993 Mar;7(3):419-28. doi: 10.1101/gad.7.3.419.
In an enhancer screen for yeast mutants that may interact with U1 small nuclear RNA (snRNA), we identified a gene that encodes the apparent yeast homolog of the well-studied human U1A protein. Both in vitro and in vivo, the absence of the protein has a dramatic effect on the activity of U1 snRNP containing the mutant U1 snRNA used in the screen. Surprisingly, the U1A gene is inessential in a wild-type U1 RNA background, as growth rate and the splicing of endogenous pre-mRNA transcripts are normal in these strains that lack the U1A protein. Even in vitro, the absence of the protein has little effect on splicing. On the basis of these observations, we suggest that a principal role of the U1A protein is to help fold or maintain U1 RNA in an active configuration.
在一项针对可能与U1小核RNA(snRNA)相互作用的酵母突变体的增强子筛选中,我们鉴定出一个基因,该基因编码已被充分研究的人类U1A蛋白明显的酵母同源物。无论在体外还是体内,该蛋白的缺失对含有筛选中使用的突变U1 snRNA的U1 snRNP的活性都有显著影响。令人惊讶的是,在野生型U1 RNA背景下,U1A基因并非必需,因为在这些缺乏U1A蛋白的菌株中,生长速率和内源性前体mRNA转录本的剪接都是正常的。即使在体外,该蛋白的缺失对剪接也几乎没有影响。基于这些观察结果,我们认为U1A蛋白的主要作用是帮助将U1 RNA折叠或维持在活性构象中。