Zahler A M, Roth M B
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98104, USA.
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2642-6. doi: 10.1073/pnas.92.7.2642.
Alternative splicing of precursor messenger RNAs (pre-mRNAs) is an important mechanism for the regulation of gene expression. The members of the SR protein family of pre-mRNA splicing factors have distinct functions in promoting alternative splice site usage. Here we show that SR proteins are required for the first step of spliceosome assembly, interaction of the U1 small nuclear ribonucleoprotein complex (U1 snRNP) with the 5' splice site of the pre-mRNA. Further, we find that individual SR proteins have distinct abilities to promote interaction of U1 snRNP with alternative 5' splice junctions. These results suggest that SR proteins direct 5' splice site selection by regulation of U1 snRNP assembly onto the pre-mRNA.
前体信使核糖核酸(前体mRNA)的可变剪接是调节基因表达的重要机制。前体mRNA剪接因子的SR蛋白家族成员在促进可变剪接位点使用方面具有不同功能。我们在此表明,SR蛋白是剪接体组装第一步所必需的,即U1小核核糖核蛋白复合体(U1 snRNP)与前体mRNA的5'剪接位点相互作用所必需的。此外,我们发现单个SR蛋白促进U1 snRNP与可变5'剪接连接相互作用的能力不同。这些结果表明,SR蛋白通过调节U1 snRNP在前体mRNA上的组装来指导5'剪接位点的选择。