Valencia Patricia, Dias Anusha P, Reed Robin
Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2008 Mar 4;105(9):3386-91. doi: 10.1073/pnas.0800250105. Epub 2008 Feb 20.
The numerous steps in protein gene expression are extensively coupled to one another through complex networks of physical and functional interactions. Indeed, >25 coupled reactions, often reciprocal, have been documented among such steps as transcription, capping, splicing, and polyadenylation. Coupling is usually not essential for gene expression, but instead enhances the rate and/or efficiency of reactions and, physiologically, may serve to increase the fidelity of gene expression. Despite numerous examples of coupling in gene expression, whether splicing enhances mRNA export still remains controversial. Although splicing was originally reported to promote export in both mammalian cells and Xenopus oocytes, it was subsequently concluded that this was not the case. These newer conclusions were surprising in light of the observations that the mRNA export machinery colocalizes with splicing factors in the nucleus and that splicing promotes recruitment of the export machinery to mRNA. We therefore reexamined the relationship between splicing and mRNA export in mammalian cells by using FISH, in combination with either transfection or nuclear microinjection of plasmid DNA. Together, these analyses indicate that both the kinetics and efficiency of mRNA export are enhanced 6- to 10-fold (depending on the construct) for spliced mRNAs relative to their cDNA counterparts. We conclude that splicing promotes mRNA export in mammalian cells and that the functional coupling between splicing and mRNA export is a conserved and general feature of gene expression in higher eukaryotes.
蛋白质基因表达的众多步骤通过复杂的物理和功能相互作用网络广泛地相互关联。实际上,在转录、加帽、剪接和聚腺苷酸化等步骤之间已记录到超过25种耦合反应,且这些反应通常是相互的。耦合通常对于基因表达并非必不可少,而是提高了反应的速率和/或效率,并且在生理上可能有助于提高基因表达的保真度。尽管基因表达中存在众多耦合的例子,但剪接是否增强mRNA输出仍存在争议。尽管最初报道剪接在哺乳动物细胞和非洲爪蟾卵母细胞中均促进输出,但随后得出的结论是并非如此。鉴于mRNA输出机制与细胞核中的剪接因子共定位以及剪接促进输出机制募集到mRNA的观察结果,这些新结论令人惊讶。因此,我们通过使用荧光原位杂交(FISH),结合质粒DNA的转染或核显微注射,重新研究了哺乳动物细胞中剪接与mRNA输出之间的关系。综合这些分析表明,相对于其cDNA对应物,剪接的mRNA的mRNA输出动力学和效率提高了6至10倍(取决于构建体)。我们得出结论,剪接促进哺乳动物细胞中的mRNA输出,并且剪接与mRNA输出之间的功能耦合是高等真核生物基因表达的保守且普遍的特征。