Rubio Mary Anne T, Rinehart Jesse J, Krett Bethany, Duvezin-Caubet Stéphane, Reichert Andreas S, Söll Dieter, Alfonzo Juan D
Department of Microbiology, Ohio State RNA Group, Ohio State University, Columbus, OH 43210-1292, USA.
Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9186-91. doi: 10.1073/pnas.0804283105. Epub 2008 Jun 27.
Mitochondrial genomes generally encode a minimal set of tRNAs necessary for protein synthesis. However, a number of eukaryotes import tRNAs from the cytoplasm into their mitochondria. For instance, Saccharomyces cerevisiae imports cytoplasmic tRNA(Gln) into the mitochondrion without any added protein factors. Here, we examine the existence of a similar active tRNA import system in mammalian mitochondria. We have used subcellular RNA fractions from rat liver and human cells to perform RT-PCR with oligonucleotide primers specific for nucleus-encoded tRNA(CUG)(Gln) and tRNA(UUG)(Gln) species, and we show that these tRNAs are present in rat and human mitochondria in vivo. Import of in vitro transcribed tRNAs, but not of heterologous RNAs, into isolated mitochondria also demonstrates that this process is tRNA-specific and does not require the addition of cytosolic factors. Although this in vitro system requires ATP, it is resistant to inhibitors of the mitochondrial electrochemical gradient, a key component of protein import. tRNA(Gln) import into mammalian mitochondria proceeds by a mechanism distinct from protein import. We also show that both tRNA(Gln) species and a bacterial pre-tRNA(Asp) can be imported in vitro into mitochondria isolated from myoclonic epilepsy with ragged-red fiber cells if provided with sufficient ATP (2 mM). This work suggests that tRNA import is more widespread than previously thought and may be a universal trait of mitochondria. Mutations in mitochondrial tRNA genes have been associated with human disease; the tRNA import system described here could possibly be exploited for the manipulation of defective mitochondria.
线粒体基因组通常编码蛋白质合成所需的一组最少的tRNA。然而,许多真核生物会将细胞质中的tRNA导入其线粒体。例如,酿酒酵母在没有任何额外蛋白质因子的情况下将细胞质tRNA(Gln)导入线粒体。在这里,我们研究了哺乳动物线粒体中是否存在类似的活性tRNA导入系统。我们使用来自大鼠肝脏和人类细胞的亚细胞RNA组分,用针对细胞核编码的tRNA(CUG)(Gln)和tRNA(UUG)(Gln)种类的寡核苷酸引物进行RT-PCR,并且我们表明这些tRNA在大鼠和人类线粒体中体内存在。将体外转录的tRNA而非异源RNA导入分离的线粒体也证明了这个过程是tRNA特异性的,并且不需要添加胞质因子。虽然这个体外系统需要ATP,但它对线粒体电化学梯度的抑制剂有抗性,而线粒体电化学梯度是蛋白质导入的关键组成部分。tRNA(Gln)导入哺乳动物线粒体的过程通过一种不同于蛋白质导入的机制进行。我们还表明,如果提供足够的ATP(2 mM),tRNA(Gln)种类和细菌前体tRNA(Asp)都可以在体外导入从肌阵挛性癫痫伴破碎红纤维细胞分离的线粒体。这项工作表明tRNA导入比以前认为的更广泛,并且可能是线粒体的一个普遍特征。线粒体tRNA基因的突变与人类疾病有关;这里描述的tRNA导入系统可能可用于操纵有缺陷的线粒体。