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Role of Nuclear Pools of Aminoacyl-tRNA Synthetases in tRNA Nuclear Export

机译:氨酰基tRNA合成酶核库在tRNA中的作用 核出口

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摘要

Reports of nuclear tRNA aminoacylation and its role in tRNA nuclear export (Lund and Dahlberg, 1998; Sarkar et al., 1999; Grosshans et al., 2000a) have led to the prediction that there should be nuclear pools of aminoacyl-tRNA synthetases. We report that in budding yeast there are nuclear pools of tyrosyl-tRNA synthetase, Tys1p. By sequence alignments we predicted a Tys1p nuclear localization sequence and showed it to be sufficient for nuclear location of a passenger protein. Mutations of this nuclear localization sequence in endogenous Tys1p reduce nuclear Tys1p pools, indicating that the motif is also important for nucleus location. The mutations do not significantly affect catalytic activity, but they do cause defects in export of tRNAs to the cytosol. Despite export defects, the cells are viable, indicating that nuclear tRNA aminoacylation is not required for all tRNA nuclear export paths. Because the tRNA nuclear exportin, Los1p, is also unessential, we tested whether tRNA aminoacylation and Los1p operate in alternative tRNA nuclear export paths. No genetic interactions between aminoacyl-tRNA synthetases and Los1p were detected, indicating that tRNA nuclear aminoacylation and Los1p operate in the same export pathway or there are more than two pathways for tRNA nuclear export.
机译:关于核tRNA氨基酰化及其在tRNA核输出中的作用的报道(Lund和Dahlberg,1998; Sarkar等,1999; Grosshans等,2000a)导致人们预测应该有氨酰基-tRNA合成酶的核库。我们报告在发芽的酵母中有酪氨酰-tRNA合成酶Tys1p的核库。通过序列比对,我们预测了Tys1p核定位序列,并表明该序列足以用于过客蛋白的核定位。内源性Tys1p中该核定位序列的突变减少了核Tys1p池,表明该基序对于核位置也很重要。突变不会显着影响催化活性,但确实会导致tRNA向细胞质输出的缺陷。尽管存在出口缺陷,但这些细胞还是有活力的,这表明并非所有tRNA核输出途径都需要核tRNA氨酰化。由于tRNA核输出蛋白Los1p也是不必要的,因此我们测试了tRNA氨酰化和Los1p是否在其他tRNA核输出路径中起作用。没有检测到氨酰基-tRNA合成酶和Los1p之间的遗传相互作用,这表明tRNA核氨基酰化和Los1p在相同的输出途径中起作用,或者tRNA核输出有两个以上的途径。

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