Suppr超能文献

5S核糖体RNA和转运RNA导入人线粒体。体外需求比较。

5 S rRNA and tRNA import into human mitochondria. Comparison of in vitro requirements.

作者信息

Entelis N S, Kolesnikova O A, Dogan S, Martin R P, Tarassov I A

机构信息

Formation de Recherche en Evolution 2375, CNRS Modèles d'Etude de Pathologies Humaines, 21 rue René Descartes, 67084 Strasbourg, France.

出版信息

J Biol Chem. 2001 Dec 7;276(49):45642-53. doi: 10.1074/jbc.M103906200. Epub 2001 Sep 10.

Abstract

In vivo, human mitochondria import 5 S rRNA and do not import tRNAs from the cytoplasm. We demonstrated previously that isolated human mitochondria are able to internalize a yeast tRNA(Lys) in the presence of yeast soluble factors. Here, we describe an assay for specific uptake of 5 S rRNA by isolated human mitochondria and compare its requirements with the artificial tRNA import. The efficiency of 5 S rRNA uptake by isolated mitochondria was comparable with that found in vivo. The import was shown to depend on ATP and the transmembrane electrochemical potential and was directed by soluble proteins. Blocking the pre-protein import channel inhibited internalization of both 5 S rRNA and tRNA, which suggests this apparatus be involved in RNA uptake by the mitochondria. We show that human mitochondria can also selectively internalize several in vitro synthesized versions of yeast tRNA(Lys) as well as a transcript of the human mitochondrial tRNA(Lys). Either yeast or human soluble proteins can direct this import, suggesting that human cells possess all factors needed for such an artificial translocation. On the other hand, the efficiency of import directed by yeast or human protein factors varies significantly, depending on the tRNA version. Similarly to the yeast system, tRNA(Lys) import into human mitochondria depended on aminoacylation and on the precursor of the mitochondrial lysyl-tRNA synthetase. 5 S rRNA import was also dependent upon soluble protein(s), which were distinct from the factors providing tRNA internalization.

摘要

在体内,人类线粒体可导入5S rRNA,但不会从细胞质中导入tRNA。我们之前证明,在酵母可溶性因子存在的情况下,分离出的人类线粒体能够内化酵母tRNA(Lys)。在此,我们描述了一种用于检测分离出的人类线粒体对5S rRNA特异性摄取的方法,并将其所需条件与人工tRNA导入所需条件进行比较。分离出的线粒体对5S rRNA的摄取效率与体内观察到的效率相当。结果表明,这种导入依赖于ATP和跨膜电化学势,并且由可溶性蛋白质引导。阻断前体蛋白导入通道会抑制5S rRNA和tRNA的内化,这表明该装置参与了线粒体对RNA的摄取。我们发现,人类线粒体还能够选择性地内化几种体外合成的酵母tRNA(Lys)版本以及人类线粒体tRNA(Lys)的转录本。酵母或人类可溶性蛋白质均可引导这种导入,这表明人类细胞具备进行这种人工转运所需的所有因子。另一方面,由酵母或人类蛋白质因子引导的导入效率根据tRNA版本的不同而有显著差异。与酵母系统类似,tRNA(Lys)导入人类线粒体依赖于氨酰化作用以及线粒体赖氨酰-tRNA合成酶的前体。5S rRNA的导入也依赖于可溶性蛋白质,这些蛋白质与促进tRNA内化的因子不同。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验