Wells S E, Neville M, Haynes M, Wang J, Igel H, Ares M
Biology Department, Sinsheimer Laboratories, University of California, Santa Cruz 95064, USA.
Genes Dev. 1996 Jan 15;10(2):220-32. doi: 10.1101/gad.10.2.220.
The function of U2 snRNA in splicing is mediated by the proteins of the U2 small nuclear ribonucleoprotein. To identify proteins that influence the function of U2 snRNA we carried out a screen for mutations in Saccharomyces cerevisiae that suppress the cold-sensitive growth defect of a mutation in U2 stem loop IIa, a structure important for the stable association of the U2 snRNP with pre-mRNA. The screen identified three dominant suppressor genes, one of which, CUS1-54, encodes an essential splicing protein required for U2 snRNP addition to the spliceosome. The suppressor protein rescues the spliceosome assembly defect of the mutant U2 in vitro, indicating that suppression is direct. Allele specificity tests show that the suppressor does not simply bypass the requirement for U2 stem loop IIa. Extra copies of wild-type CUS1, but not CUS1-54, suppress the temperature-sensitive prp11 and prp5 mutations, linking CUS1 protein to a subset of other factors required at the same step of spliceosome assembly. CUS1 is homologous to SAP 145, a component of the mammalian U2 snRNP that interacts with pre-mRNA. The yeast genome also encodes a homolog of human SAP 49, a protein that interacts strongly with both SAP 145 and pre-mRNA, underscoring the conservation of U2 snRNP proteins that function in spliceosome assembly.
U2小核RNA(snRNA)在剪接过程中的功能是由U2小核糖核蛋白中的蛋白质介导的。为了鉴定影响U2 snRNA功能的蛋白质,我们在酿酒酵母中进行了筛选,寻找能抑制U2茎环IIa突变体冷敏感生长缺陷的突变,U2茎环IIa是U2 snRNP与前体mRNA稳定结合的重要结构。筛选鉴定出三个显性抑制基因,其中一个基因CUS1 - 54编码一种将U2 snRNP添加到剪接体中所需的必需剪接蛋白。该抑制蛋白在体外挽救了突变体U2的剪接体组装缺陷,表明抑制作用是直接的。等位基因特异性测试表明,该抑制因子并非简单地绕过对U2茎环IIa的需求。野生型CUS1的额外拷贝(而非CUS1 - 54)能抑制温度敏感型prp11和prp5突变,这将CUS1蛋白与剪接体组装同一步骤所需的其他部分因子联系起来。CUS1与哺乳动物U2 snRNP中与前体mRNA相互作用的成分SAP 145同源。酵母基因组还编码人类SAP 49的同源物,SAP 49是一种与SAP 145和前体mRNA都强烈相互作用的蛋白质,这突出了在剪接体组装中起作用的U2 snRNP蛋白的保守性。