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tRNAs 和蛋白质使用相同的进口通道在原生动物线粒体的外膜间移位。

tRNAs and proteins use the same import channel for translocation across the mitochondrial outer membrane of trypanosomes.

机构信息

Department of Chemistry and Biochemistry, University of Bern, Bern CH-3012, Switzerland.

Department of Biochemistry and Functional Proteomics, Institute of Biology II, Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2017 Sep 12;114(37):E7679-E7687. doi: 10.1073/pnas.1711430114. Epub 2017 Aug 28.

Abstract

Mitochondrial tRNA import is widespread, but the mechanism by which tRNAs are imported remains largely unknown. The mitochondrion of the parasitic protozoan lacks tRNA genes, and thus imports all tRNAs from the cytosol. Here we show that in in vivo import of tRNAs requires four subunits of the mitochondrial outer membrane protein translocase but not the two receptor subunits, one of which is essential for protein import. The latter shows that it is possible to uncouple mitochondrial tRNA import from protein import. Ablation of the intermembrane space domain of the translocase subunit, archaic translocase of the outer membrane (ATOM)14, on the other hand, while not affecting the architecture of the translocase, impedes both protein and tRNA import. A protein import intermediate arrested in the translocation channel prevents both protein and tRNA import. In the presence of tRNA, blocking events of single-channel currents through the pore formed by recombinant ATOM40 were detected in electrophysiological recordings. These results indicate that both types of macromolecules use the same import channel across the outer membrane. However, while tRNA import depends on the core subunits of the protein import translocase, it does not require the protein import receptors, indicating that the two processes are not mechanistically linked.

摘要

线粒体 tRNA 导入是广泛存在的,但 tRNA 导入的机制在很大程度上仍是未知的。寄生原生动物 的线粒体缺乏 tRNA 基因,因此从细胞质中导入所有 tRNA。在这里,我们表明 在体内导入 tRNA 需要线粒体外膜蛋白转运体的四个亚基,但不需要两个受体亚基,其中一个对于蛋白质导入是必需的。后者表明,可以将线粒体 tRNA 导入与蛋白质导入分离。另一方面,外膜古老转运体(ATOM)14 的跨膜空间结构域的缺失虽然不影响转运体的结构,但会阻碍蛋白质和 tRNA 的导入。在蛋白质导入中间物被截留在易位通道中时,会阻止蛋白质和 tRNA 的导入。在存在 tRNA 的情况下,通过重组 ATOM40 形成的孔的单通道电流阻断事件在电生理记录中被检测到。这些结果表明,这两种类型的大分子都使用穿过外膜的相同导入通道。然而,虽然 tRNA 导入依赖于蛋白质导入转运体的核心亚基,但它不需要蛋白质导入受体,这表明这两个过程在机制上没有联系。

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