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布氏锥虫的一种核编码tRNA被导入线粒体。

A nuclear encoded tRNA of Trypanosoma brucei is imported into mitochondria.

作者信息

Schneider A, Martin J, Agabian N

机构信息

Intercampus Program in Molecular Parasitology, University of California, San Francisco.

出版信息

Mol Cell Biol. 1994 Apr;14(4):2317-22. doi: 10.1128/mcb.14.4.2317-2322.1994.

Abstract

The mitochondrial genome of trypanosomes, unlike that of most other eukaryotes, does not appear to encode any tRNAs. Therefore, mitochondrial tRNAs must be either imported into the organelle or created through a novel mitochondrial process, such as RNA editing. Trypanosomal tRNA(Tyr), whose gene contains an 11-nucleotide intron, is present in both the cytosol and the mitochondrion and is encoded by a single-copy nuclear gene. By site-directed mutagenesis, point mutations were introduced into this tRNA gene, and the mutated gene was reintroduced into the trypanosomal nuclear genome by DNA transfection. Expression of the mutant tRNA led to the accumulation of unspliced tRNA(Tyr) (A. Schneider, K. P. McNally, and N. Agabian, J. Biol. Chem. 268:21868-21874, 1993). Cell fractionation revealed that a significant portion of the unspliced mutant tRNA(Tyr) was recovered in the mitochondrial fraction and was resistant to micrococcal nuclease treatment in the intact organelle. Expression of the nuclear integrated, mutated tRNA gene and recovery of its gene product in the mitochondrial fraction directly demonstrated import. In vitro experiments showed that the unspliced mutant tRNA(Tyr), in contrast to the spliced wild-type form, was no longer a substrate for the cognate aminoacyl synthetase. The presence of uncharged tRNA in the mitochondria demonstrated that aminoacylation was not coupled to import.

摘要

与大多数其他真核生物不同,锥虫的线粒体基因组似乎不编码任何转运RNA(tRNA)。因此,线粒体tRNA必定要么被导入该细胞器,要么通过一种新的线粒体过程产生,比如RNA编辑。锥虫的tRNA(Tyr)基因含有一个11个核苷酸的内含子,它同时存在于细胞质和线粒体中,由一个单拷贝核基因编码。通过定点诱变,将点突变引入该tRNA基因,然后通过DNA转染将突变基因重新导入锥虫核基因组。突变tRNA的表达导致未剪接的tRNA(Tyr)积累(A. 施奈德、K.P. 麦克纳利和N. 阿加比安,《生物化学杂志》268:21868 - 21874,1993)。细胞分级分离显示,很大一部分未剪接的突变tRNA(Tyr)在线粒体分级部分中被回收,并且在完整的细胞器中对微球菌核酸酶处理具有抗性。核整合的突变tRNA基因的表达及其基因产物在线粒体分级部分中的回收直接证明了其被导入。体外实验表明,与剪接后的野生型形式相比,未剪接的突变tRNA(Tyr)不再是同源氨酰基合成酶的底物。线粒体中存在未带电的tRNA表明氨酰化与导入没有关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb17/358598/1ac2d24688f8/molcellb00004-0107-a.jpg

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