Steiner-Mosonyi Marta, Leslie Deena M, Dehghani Hesam, Aitchison John D, Mangroo Dev
Guelph-Waterloo Center for Graduate Work in Chemistry and Biochemistry, Department of Chemistry and Biochemistry, University of Guelph, Ontario N1G 2W1, Canada.
J Biol Chem. 2003 Aug 22;278(34):32236-45. doi: 10.1074/jbc.M302779200. Epub 2003 Jun 6.
A yeast tRNA three-hybrid interaction approach and an in vivo nuclear tRNA export assay based on amber suppression was used to identify proteins that participate in the nuclear tRNA export process in Saccharomyces cerevisiae. One of the proteins identified by this strategy is Utp8p, an essential 80-kDa nucleolar protein that has been implicated in 18 S ribosomal RNA biogenesis. Our characterization indicated that the major function of Utp8p is in nuclear tRNA export. Like the S. cerevisiae Los1p and the mammalian exportin-t, which are proteins known to facilitate nuclear tRNA export, overexpression of Utp8p restored export of tRNAamTyr mutants defective in nuclear export. Furthermore, depletion of Utp8p blocked nuclear export of mature tRNAs derived from both intronless and intron-containing pre-tRNAs but did not affect tRNA and rRNA maturation, nuclear export of mRNA and ribosomes, or nuclear tRNA aminoacylation. Overexpression of Utp8p also alleviated nuclear retention of non-aminoacylated tRNATyr in a tyrosyl-tRNA synthetase mutant strain. Utp8p binds tRNA directly and saturably, indicating that it has a tRNA-binding site. Utp8p does not appear to function as a tRNA export receptor, because it does not shuttle between the nucleus and the cytoplasm. Taken together, the results suggest that Utp8p is an essential intranuclear component of the nuclear tRNA export machinery, which may channel tRNA to the various tRNA export pathways operating in S. cerevisiae.
采用酵母tRNA三杂交相互作用方法以及基于琥珀抑制的体内细胞核tRNA输出分析,来鉴定参与酿酒酵母细胞核tRNA输出过程的蛋白质。通过该策略鉴定出的一种蛋白质是Utp8p,它是一种必需的80 kDa核仁蛋白,与18 S核糖体RNA生物合成有关。我们的表征表明,Utp8p的主要功能在于细胞核tRNA输出。与已知促进细胞核tRNA输出的酿酒酵母Los1p和哺乳动物输出蛋白t一样,Utp8p的过表达恢复了在细胞核输出方面存在缺陷的tRNAamTyr突变体的输出。此外,Utp8p的缺失阻断了源自无内含子和含内含子前体tRNA的成熟tRNA的细胞核输出,但不影响tRNA和rRNA的成熟、mRNA和核糖体的细胞核输出或细胞核tRNA的氨酰化。Utp8p的过表达还缓解了酪氨酰-tRNA合成酶突变体菌株中非氨酰化tRNATyr的细胞核滞留。Utp8p直接且可饱和地结合tRNA,表明它具有一个tRNA结合位点。Utp8p似乎并不作为tRNA输出受体发挥作用,因为它不会在细胞核和细胞质之间穿梭。综上所述,结果表明Utp8p是细胞核tRNA输出机制的一个必需的核内组分,它可能将tRNA导向酿酒酵母中运行的各种tRNA输出途径。