Department of Molecular and Cellular Genetics, UMR 7156 Génétique Moléculaire, Génomique, Microbiologie (GMGM), CNRS-Université de Strasbourg, Strasbourg, France.
PLoS One. 2013 Jun 14;8(6):e66228. doi: 10.1371/journal.pone.0066228. Print 2013.
In human cell, a subset of small non-coding RNAs is imported into mitochondria from the cytosol. Analysis of the tRNA import pathway allowing targeting of the yeast tRNA(Lys)(CUU) into human mitochondria demonstrates a similarity between the RNA import mechanisms in yeast and human cells. We show that the cytosolic precursor of human mitochondrial lysyl-tRNA synthetase (preKARS2) interacts with the yeast tRNA(Lys)(CUU) and small artificial RNAs which contain the structural elements determining the tRNA mitochondrial import, and facilitates their internalization by isolated human mitochondria. The tRNA import efficiency increased upon addition of the glycolytic enzyme enolase, previously found to be an actor of the yeast RNA import machinery. Finally, the role of preKARS2 in the RNA mitochondrial import has been directly demonstrated in vivo, in cultured human cells transfected with the yeast tRNA and artificial importable RNA molecules, in combination with preKARS2 overexpression or downregulation by RNA interference. These findings suggest that the requirement of protein factors for the RNA mitochondrial targeting might be a conserved feature of the RNA import pathway in different organisms.
在人类细胞中,一小部分小的非编码 RNA 从细胞质被导入到线粒体中。对允许酵母 tRNA(Lys)(CUU)靶向进入人线粒体的 tRNA 导入途径的分析表明,酵母和人类细胞中的 RNA 导入机制之间存在相似性。我们表明,人线粒体赖氨酸-tRNA 合成酶(preKARS2)的细胞质前体与酵母 tRNA(Lys)(CUU)和包含决定 tRNA 线粒体导入的结构元件的小人工 RNA 相互作用,并促进它们被分离的人线粒体内化。添加糖酵解酶烯醇酶后,tRNA 导入效率增加,先前发现该酶是酵母 RNA 导入机制的一个因子。最后,通过在转染了酵母 tRNA 和可导入人工 RNA 分子的培养的人细胞中进行 RNA 干扰,直接证明了 preKARS2 在 RNA 线粒体导入中的作用。这些发现表明,对于 RNA 线粒体靶向的蛋白质因子的需求可能是不同生物体中 RNA 导入途径的保守特征。