Tarasov I A, Entelis N S, Krasheninnikov I A
Biokhimiia. 1993 Oct;58(10):1493-502.
To study the mechanisms of targeting tRNA(CUULys) from the cytoplasm into the mitochondrial compartment of the yeast cells, two test systems have been developed. The in vivo system based on the electroporation of intact yeast cells was used to introduce labelled tRNAs into the cytoplasm; however, only tRNA(CUULys) was found in the mitochondrial compartment. The in vitro import of this tRNA into isolated mitochondria required the presence of ATP and soluble cellular proteins in the reaction mixture. Two protein fractions were found to be necessary to direct the import in vitro. The first one had a high heparin-binding affinity, while the other one was not retained on heparin-Sepharose. Aminoacylation of the tRNA(Lys) before the transport and/or addition of the correspondent lysyl-tRNA synthetase to the in vitro system increased the efficiency of the import, but the protein fraction with heparin-binding properties is still required. The unmodified transcripts of the tRNA(CUULys) gene were shown to be able to be transported into isolated yeast mitochondria.
为了研究将酵母细胞胞质中的tRNA(CUU Lys)靶向转运至线粒体区室的机制,已开发了两种测试系统。基于完整酵母细胞电穿孔的体内系统用于将标记的tRNA导入胞质;然而,仅在 mitochondrial compartment中发现了tRNA(CUU Lys)。将这种tRNA体外导入分离的线粒体需要反应混合物中存在ATP和可溶性细胞蛋白。发现有两个蛋白质组分对于体外指导转运是必需的。第一个具有高肝素结合亲和力,而另一个不保留在肝素-琼脂糖上。在转运前对tRNA(Lys)进行氨酰化和/或将相应的赖氨酰-tRNA合成酶添加到体外系统中可提高转运效率,但仍需要具有肝素结合特性的蛋白质组分。已证明tRNA(CUU Lys)基因的未修饰转录本能够被转运到分离的酵母线粒体中。