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Genetics. 1987 Apr;115(4):637-47. doi: 10.1093/genetics/115.4.637.
2
Translational regulation of mitochondrial gene expression by nuclear genes of Saccharomyces cerevisiae.酿酒酵母核基因对线粒体基因表达的翻译调控
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3
PET111 acts in the 5'-leader of the Saccharomyces cerevisiae mitochondrial COX2 mRNA to promote its translation.PET111作用于酿酒酵母线粒体COX2 mRNA的5'前导序列,以促进其翻译。
Genetics. 1993 Mar;133(3):509-16. doi: 10.1093/genetics/133.3.509.
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Alteration of the Saccharomyces cerevisiae COX2 mRNA 5'-untranslated leader by mitochondrial gene replacement and functional interaction with the translational activator protein PET111.通过线粒体基因置换改变酿酒酵母COX2 mRNA 5'-非翻译前导序列及其与翻译激活蛋白PET111的功能相互作用。
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Saccharomyces cerevisiae positive regulatory gene PET111 encodes a mitochondrial protein that is translated from an mRNA with a long 5' leader.酿酒酵母阳性调控基因PET111编码一种线粒体蛋白,该蛋白由具有长5'前导序列的mRNA翻译而来。
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Yeast mitochondrial protein Pet111p binds directly to two distinct targets in mRNA, suggesting a mechanism of translational activation.酵母线粒体蛋白 Pet111p 直接结合到 mRNA 中的两个不同靶标,提示了一种翻译激活的机制。
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The Schizosaccharomyces pombe PPR protein Ppr10 associates with a novel protein Mpa1 and acts as a mitochondrial translational activator.粟酒裂殖酵母PPR蛋白Ppr10与一种新蛋白Mpa1结合,并作为线粒体翻译激活因子发挥作用。
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Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis.通过正交交变电场凝胶电泳从酵母中分离染色体DNA分子。
Nucleic Acids Res. 1984 Jul 25;12(14):5647-64. doi: 10.1093/nar/12.14.5647.
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Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis.通过脉冲场梯度凝胶电泳分离酵母染色体大小的DNA。
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Mitochondrial translation products during release from glucose repression in Saccharomyces cerevisiae.酿酒酵母从葡萄糖阻遏释放过程中的线粒体翻译产物。
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A nuclear mutation that post-transcriptionally blocks accumulation of a yeast mitochondrial gene product can be suppressed by a mitochondrial gene rearrangement.一种转录后阻断酵母线粒体基因产物积累的核突变可被线粒体基因重排所抑制。
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One-step gene disruption in yeast.酵母中的一步基因破坏
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Assembly of the mitochondrial membrane system. Structure and nucleotide sequence of the gene coding for subunit 1 of yeast cytochrme oxidase.线粒体膜系统的组装。酵母细胞色素氧化酶亚基1编码基因的结构与核苷酸序列。
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Two nuclear mutations that block mitochondrial protein import in yeast.两个阻断酵母线粒体蛋白导入的核突变。
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Plastid translation in organello and in vitro during light-induced development in Euglena.眼虫在光诱导发育过程中质体在细胞器内及体外的翻译。
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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.

DOI:10.1093/genetics/115.4.637
PMID:3034718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1203096/
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。