Blanchette Marco, Labourier Emmanuel, Green Richard E, Brenner Steven E, Rio Donald C
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Mol Cell. 2004 Jun 18;14(6):775-86. doi: 10.1016/j.molcel.2004.06.012.
The protein factor U2AF is an essential component required for pre-mRNA splicing. Mutations identified in the S. pombe large U2AF subunit were used to engineer transgenic Drosophila carrying temperature-sensitive U2AF large subunit alleles. Mutant recombinant U2AF heterodimers showed reduced polypyrimidine tract RNA binding at elevated temperatures. Genome-wide RNA profiling comparing wild-type and mutant strains identified more than 400 genes differentially expressed in the dU2AF50 mutant flies grown at the restrictive temperature. Surprisingly, almost 40% of the downregulated genes lack introns. Microarray analyses revealed that nuclear export of a large number of intronless mRNAs is impaired in Drosophila-cultured cells RNAi knocked down for dU2AF50. Immunopurification of nuclear RNP complexes showed that dU2AF50 associates with intronless mRNAs. These results reveal an unexpected role for the splicing factor dU2AF50 in the nuclear export of intronless mRNAs.
蛋白质因子U2AF是前体mRNA剪接所需的重要组成部分。在粟酒裂殖酵母大U2AF亚基中鉴定出的突变被用于构建携带温度敏感型U2AF大亚基等位基因的转基因果蝇。突变的重组U2AF异二聚体在温度升高时显示出与聚嘧啶序列RNA的结合减少。对野生型和突变株进行全基因组RNA分析,发现在限制温度下生长的dU2AF50突变果蝇中有400多个基因表达差异。令人惊讶的是,几乎40%的下调基因没有内含子。微阵列分析显示,在针对dU2AF50进行RNA干扰的果蝇培养细胞中,大量无内含子mRNA的核输出受损。核RNP复合物的免疫纯化表明,dU2AF50与无内含子mRNA相关联。这些结果揭示了剪接因子dU2AF50在无内含子mRNA核输出中的意外作用。