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PET111,酿酒酵母中的一个核基因,是线粒体中编码细胞色素c氧化酶亚基II的mRNA翻译所必需的。

PET111, a Saccharomyces cerevisiae nuclear gene required for translation of the mitochondrial mRNA encoding cytochrome c oxidase subunit II.

作者信息

Poutre C G, Fox T D

出版信息

Genetics. 1987 Apr;115(4):637-47. doi: 10.1093/genetics/115.4.637.

Abstract

Mutations in the nuclear gene PET111 are recessive and specifically block accumulation of cytochrome c oxidase subunit II (coxII), the product of a mitochondrial gene. However, the coxII mRNA is present in pet111 mutants at a level approximately one-third that of wild type. The simplest explanation for this phenotype is that PET111 is required for translation of the coxII mRNA. The reduced steady-state level of this mRNA is probably a secondary effect, caused by increased degradation of the untranslated transcript. Mitochondrial suppressors of pet111, carried on rho-mtDNAs, bypass the requirement for PET111 in coxII translation. Three suppressors are fusions between the coxII structural gene and other mitochondrial genes, that encode chimeric proteins consisting of the N-terminal portions of other mitochondrially coded proteins fused to the coxII precursor protein. When present together with rho+ mtDNA in a heteroplasmic state, these suppressors allow coxII synthesis in pet111 mutants. Thus in wild type, the PET111 product, or something under its control, probably acts at a site coded in the proximal portion of the gene for coxII to promote translation of the mRNA. PET111 was isolated by molecular cloning and genetically mapped to a position approximately midway between rna1 and SUP8 on chromosome XIII.

摘要

核基因PET111中的突变是隐性的,它会特异性地阻断细胞色素c氧化酶亚基II(coxII,一种线粒体基因的产物)的积累。然而,pet111突变体中coxII mRNA的水平约为野生型的三分之一。对这种表型最简单的解释是,PET111是coxII mRNA翻译所必需的。这种mRNA稳态水平的降低可能是一种次级效应,由未翻译转录本的降解增加所致。携带在rho - mtDNA上的pet111线粒体抑制子绕过了coxII翻译中对PET111的需求。三种抑制子是coxII结构基因与其他线粒体基因的融合体,它们编码嵌合蛋白,这些嵌合蛋白由其他线粒体编码蛋白的N端部分与coxII前体蛋白融合而成。当与rho + mtDNA以异质状态共同存在时,这些抑制子可使pet111突变体中合成coxII。因此在野生型中,PET111产物或其控制的某种物质可能作用于coxII基因近端部分编码的位点,以促进mRNA的翻译。PET111通过分子克隆分离得到,并通过遗传定位到第十三号染色体上rna1和SUP8之间大约中间的位置。

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