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Genome-wide deletion mutant analysis reveals genes required for respiratory growth, mitochondrial genome maintenance and mitochondrial protein synthesis in Saccharomyces cerevisiae

机译:全基因组缺失突变体分析揭示了酿酒酵母中呼吸生长,线粒体基因组维持和线粒体蛋白质合成所需的基因

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ABSTRACT: BACKGROUND: The mitochondrial respiratory chain produces metabolic energy by oxidative phosphorylation. Biogenesis of the respiratory chain requires the coordinated expression of two genomes: the nuclear genome encoding the vast majority of mitochondrial proteins, and the mitochondrial genome encoding a handful of mitochondrial proteins. The understanding of the molecular processes contributing to respiratory chain assembly and maintenance requires the systematic identification and functional analysis of the genes involved. RESULTS: We pursued a systematic, genome-wide approach to define the sets of genes required for respiratory activity and maintenance and expression of the mitochondrial genome in yeast. By comparative gene deletion analysis we found an unexpected phenotypic plasticity among respiratory-deficient mutants, and we identified ten previously uncharacterized genes essential for respiratory growth (RRG1 through RRG10). Systematic functional analysis of 319 respiratory-deficient mutants revealed 16 genes essential for maintenance of the mitochondrial genome, 88 genes required for mitochondrial protein translation, and 10 genes required for expression of specific mitochondrial gene products. A group of mutants acquiring irreversible damage compromising respiratory capacity includes strains defective in assembly of the cytochrome c oxidase that were found to be particularly sensitive to aging. CONCLUSIONS: These data advance the understanding of the molecular processes contributing to maintenance of the mitochondrial genome, mitochondrial protein translation, and assembly of the respiratory chain. They revealed a number of previously uncharacterized components, and provide a comprehensive picture of the molecular processes required for respiratory activity in a simple eukaryotic cell.
机译:摘要:背景:线粒体呼吸链通过氧化磷酸化产生代谢能量。呼吸链的生物发生需要两个基因组的协同表达:编码绝大多数线粒体蛋白质的核基因组,以及编码少数线粒体蛋白质的线粒体基因组。对有助于呼吸链组装和维持的分子过程的理解要求对涉及的基因进行系统的鉴定和功能分析。结果:我们追求一种系统的,全基因组的方法来定义呼吸活动以及维持和表达酵母中线粒体基因组所需的基因集。通过比较性基因缺失分析,我们发现呼吸缺陷型突变体具有意想不到的表型可塑性,并且我们鉴定了十个以前未表征的基因,这些基因对于呼吸生长至关重要(RRG1至RRG10)。对319个呼吸缺陷型突变体的系统功能分析显示,维护线粒体基因组必不可少的16个基因,线粒体蛋白质翻译所需的88个基因和表达特定线粒体基因产物所需的10个基因。一组损害呼吸能力的不可逆损伤的突变体包括发现对衰老特别敏感的细胞色素C氧化酶组装缺陷的菌株。结论:这些数据促进了对分子过程的理解,这些分子过程有助于维持线粒体基因组,线粒体蛋白翻译和呼吸链的组装。他们揭示了许多以前未表征的成分,并提供了一个简单的真核细胞中呼吸活动所需的分子过程的全面描述。

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