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酿酒酵母中线粒体COX3基因表达所需的核PET122基因的分子克隆及核苷酸序列

Molecular cloning and nucleotide sequence of the nuclear PET122 gene required for expression of the mitochondrial COX3 gene in S. cerevisiae.

作者信息

Ohmen J D, Kloeckener-Gruissem B, McEwen J E

机构信息

Department of Microbiology, University of California, Los Angeles 90024.

出版信息

Nucleic Acids Res. 1988 Nov 25;16(22):10783-802. doi: 10.1093/nar/16.22.10783.

Abstract

The nuclear PET122 gene from S. cerevisiae is necessary for translation of a single mitochondrial mRNA that encodes subunit III of cytochrome c oxidase. We report here the cloning and nucleotide sequence of PET122, and properties of the predicted protein product, which consists of 242 residues. Analysis of PET122-lacZ translational fusions confirms that the PET122 coding region is translated in vivo and indicates that the PET122 protein product is targeted to mitochondria. A 117 residue domain located in the carboxy-terminal half of the PET122 protein, at least part of which is shown by characterization of mutants to be critical for PET122 function, exhibits 24% identity and 59% similarity to a portion of the catalytic domain of E. coli alanyl-tRNA synthetase. However, pet122 mutants are not defective in mitochondrial translation per se, as would be expected if PET122 encoded a tRNA synthetase. Instead, the PET122 protein may carry out one or more activities in common with tRNA synthetases, such as binding of ATP or RNA.

摘要

酿酒酵母的核基因PET122对于单个线粒体mRNA的翻译是必需的,该mRNA编码细胞色素c氧化酶的亚基III。我们在此报告PET122的克隆和核苷酸序列,以及预测的由242个残基组成的蛋白质产物的特性。对PET122-lacZ翻译融合体的分析证实PET122编码区在体内被翻译,并表明PET122蛋白产物定位于线粒体。位于PET122蛋白羧基末端一半的117个残基结构域,通过突变体表征显示其至少部分对于PET122功能至关重要,该结构域与大肠杆菌丙氨酰-tRNA合成酶催化结构域的一部分具有24%的同一性和59%的相似性。然而,pet122突变体本身在线粒体翻译方面并无缺陷,而如果PET122编码一种tRNA合成酶,情况则会相反。相反,PET122蛋白可能执行与tRNA合成酶共有的一种或多种活动,例如ATP或RNA的结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8857/338939/2ca5f4e13b9e/nar00164-0385-a.jpg

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