Moy T I, Silver P A
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and The Dana-Farber Cancer Institute, Boston, Massachusetts 02115 USA.
Genes Dev. 1999 Aug 15;13(16):2118-33. doi: 10.1101/gad.13.16.2118.
After their assembly in the nucleolus, ribosomal subunits are exported from the nucleus to the cytoplasm. After export, the 20S rRNA in the small ribosomal subunit is cleaved to yield 18S rRNA and the small 5' ITS1 fragment. The 5' ITS1 RNA is normally degraded by the cytoplasmic Xrn1 exonuclease, but in strains lacking XRN1, the 5' ITS1 fragment accumulates in the cytoplasm. Using the cytoplasmic localization of the 5' ITS1 fragment as an indicator for the export of the small ribosomal subunit, we have identified genes that are required for ribosome export. Ribosome export is dependent on the Ran-GTPase as mutations in Ran or its regulators caused 5' ITS1 to accumulate in the nucleoplasm. Mutations in the genes encoding the nucleoporin Nup82 and in the NES exporter Xpo1/Crm1 also caused the nucleoplasmic accumulation of 5' ITS1. Mutants in a subset of nucleoporins and in the nuclear transport factors Srp1, Kap95, Pse1, Cse1, and Mtr10 accumulate the 5' ITS1 in the nucleolus and affect ribosome assembly. In contrast, we did not detect nuclear accumulation of 5' ITS1 in 28 yeast strains that have mutations in other genes affecting nuclear trafficking.
核糖体亚基在核仁中组装完成后,从细胞核输出到细胞质。输出后,小核糖体亚基中的20S rRNA被切割产生18S rRNA和小的5' ITS1片段。5' ITS1 RNA通常会被细胞质中的Xrn1核酸外切酶降解,但在缺乏XRN1的菌株中,5' ITS1片段会在细胞质中积累。利用5' ITS1片段的细胞质定位作为小核糖体亚基输出的指标,我们鉴定出了核糖体输出所需的基因。核糖体输出依赖于Ran-GTP酶,因为Ran或其调节因子的突变会导致5' ITS1在核质中积累。编码核孔蛋白Nup82和NES输出蛋白Xpo1/Crm1的基因发生突变,也会导致5' ITS1在核质中积累。一部分核孔蛋白以及核转运因子Srp1、Kap95、Pse1、Cse1和Mtr10的突变体,会使5' ITS1在核仁中积累并影响核糖体组装。相比之下,在其他影响核运输的基因发生突变的28个酵母菌株中,我们未检测到5' ITS1的核内积累。