Farny Natalie G, Hurt Jessica A, Silver Pamela A
Department of Systems Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2008 Jan 1;22(1):66-78. doi: 10.1101/gad.1616008. Epub 2007 Dec 17.
Eukaryotic gene expression requires export of messenger RNAs (mRNAs) from their site of transcription in the nucleus to the cytoplasm where they are translated. While mRNA export has been studied in yeast, the complexity of gene structure and cellular function in metazoan cells has likely led to increased diversification of these organisms' export pathways. Here we report the results of a genome-wide RNAi screen in which we identify 72 factors required for polyadenylated [poly-(A(+))] mRNA export from the nucleus in Drosophila cells. Using structural and functional conservation analysis of yeast and Drosophila mRNA export factors, we expose the evolutionary divergence of eukaryotic mRNA export pathways. Additionally, we demonstrate the differential export requirements of two endogenous heat-inducible transcripts--intronless heat-shock protein 70 (HSP70) and intron-containing HSP83--and identify novel export factors that participate in HSP83 mRNA splicing. We characterize several novel factors and demonstrate their participation in interactions with known components of the Drosophila export machinery. One of these factors, Drosophila melanogaster PCI domain-containing protein 2 (dmPCID2), associates with polysomes and may bridge the transition between exported messenger ribonucleoprotein particles (mRNPs) and polysomes. Our results define the global network of factors involved in Drosophila mRNA export, reveal specificity in the export requirements of different transcripts, and expose new avenues for future work in mRNA export.
真核基因表达需要信使核糖核酸(mRNA)从细胞核内的转录位点输出到细胞质中进行翻译。虽然在酵母中对mRNA输出进行了研究,但后生动物细胞中基因结构和细胞功能的复杂性可能导致这些生物的输出途径更加多样化。在此,我们报告了一项全基因组RNA干扰筛选的结果,其中我们鉴定出果蝇细胞中从细胞核输出多聚腺苷酸化[poly-(A(+))]mRNA所需的72个因子。通过对酵母和果蝇mRNA输出因子进行结构和功能保守性分析,我们揭示了真核mRNA输出途径的进化差异。此外,我们证明了两种内源性热诱导转录本——无内含子热休克蛋白70(HSP70)和含内含子的HSP83——的不同输出需求,并鉴定出参与HSP83 mRNA剪接的新型输出因子。我们对几个新因子进行了表征,并证明它们参与了与果蝇输出机制已知成分的相互作用。其中一个因子,果蝇含PCI结构域蛋白2(dmPCID2),与多核糖体相关,可能在输出的信使核糖核蛋白颗粒(mRNP)和多核糖体之间的转变中起桥梁作用。我们的结果确定了参与果蝇mRNA输出的因子的全局网络,揭示了不同转录本输出需求的特异性,并为mRNA输出的未来研究开辟了新途径。