Brodsky A S, Silver P A
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and The Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
RNA. 2000 Dec;6(12):1737-49. doi: 10.1017/s1355838200001059.
RNA export from the nucleus is thought to be linked to proper processing and packaging into ribonucleoprotein protein complexes. A system to observe mRNA nuclear export in living yeast cells was developed by fusing the U1A RNA-binding protein to the green fluorescent protein to follow specific mRNAs with U1A hairpins engineered into them. RNAs encoding Rpl25, Pgk1, and Ssa4 were examined for the effects of 3' UTRs, introns, RNA processing factors, nucleoporins, and transport factors on their export. All accumulated in the nucleus in mutants affecting components of the nuclear export machinery and certain nucleoporins. However, under conditions of stress, PGK1 and RPL25 transcripts accumulate in the nucleus whereas SSA4 RNA is exported. Moreover, when export is blocked, only RNAs containing the ASH1 3' UTR accumulated in the nucleolus. Mutations in the splicing machinery selectively blocked export of only intron-containing RNAs. Mutations in RNA14, RNA15, and PAP1, which encode factors important for 3' processing, also blocked export of all RNAs, including SSA4, thereby linking export to the process of polyadenlyation. Taken together, these data graphically display the connections between mRNA processing and nuclear export.
细胞核中的RNA输出被认为与正确的加工以及包装进核糖核蛋白复合物有关。通过将U1A RNA结合蛋白与绿色荧光蛋白融合,以追踪其中设计有U1A发夹结构的特定mRNA,从而开发出一种在活酵母细胞中观察mRNA细胞核输出的系统。研究了编码Rpl25、Pgk1和Ssa4的RNA,以考察3'非翻译区(UTR)、内含子、RNA加工因子、核孔蛋白和转运因子对其输出的影响。在影响细胞核输出机制组分和某些核孔蛋白的突变体中,所有这些RNA都在细胞核中积累。然而,在应激条件下,PGK1和RPL25转录本在细胞核中积累,而SSA4 RNA则被输出。此外,当输出受阻时,只有含有ASH1 3' UTR的RNA在核仁中积累。剪接机制中的突变选择性地仅阻断含内含子RNA的输出。编码对3'加工重要的因子的RNA14、RNA15和PAP1中的突变,也阻断了包括SSA4在内的所有RNA的输出,从而将输出与聚腺苷酸化过程联系起来。综上所述,这些数据形象地展示了mRNA加工与细胞核输出之间的联系。