Stenger Maria, Le Duc Tung, Klecker Till, Westermann Benedikt
Zellbiologie, Universität Bayreuth, 95440 Bayreuth, Germany.
Microb Cell. 2020 Jun 30;7(9):234-249. doi: 10.15698/mic2020.09.729.
The production of metabolic energy in form of ATP by oxidative phosphorylation depends on the coordinated action of hundreds of nuclear-encoded mitochondrial proteins and a handful of proteins encoded by the mitochondrial genome (mtDNA). We used the yeast as a model system to systematically identify the genes contributing to this process. Integration of genome-wide high-throughput growth assays with previously published large data sets allowed us to define with high confidence a set of 254 nuclear genes that are indispensable for respiratory growth. Next, we induced loss of mtDNA in the yeast deletion collection by growth on ethidium bromide-containing medium and identified twelve genes that are essential for viability in the absence of mtDNA (i.e. -negative). Replenishment of mtDNA by cytoduction showed that respiratory-deficient phenotypes are highly variable in many yeast mutants. Using a mitochondrial genome carrying a selectable marker, , we screened for mutants that are specifically defective in maintenance of mtDNA and mitochondrial protein synthesis. We found that up to 176 nuclear genes are required for expression of mitochondria-encoded proteins during fermentative growth. Taken together, our data provide a comprehensive picture of the molecular processes that are required for respiratory metabolism in a simple eukaryotic cell.
通过氧化磷酸化产生ATP形式的代谢能量取决于数百种核编码的线粒体蛋白和少数由线粒体基因组(mtDNA)编码的蛋白的协同作用。我们以酵母为模型系统,系统地鉴定了参与这一过程的基因。将全基因组高通量生长测定与先前发表的大型数据集相结合,使我们能够高度自信地定义一组254个对呼吸生长不可或缺的核基因。接下来,我们通过在含溴化乙锭的培养基上生长,在酵母缺失文库中诱导mtDNA缺失,并鉴定了12个在没有mtDNA时(即ρ0)对生存能力至关重要的基因。通过细胞融合补充mtDNA表明,许多酵母突变体中的呼吸缺陷表型高度可变。使用携带选择标记的线粒体基因组,我们筛选了在mtDNA维持和线粒体蛋白质合成方面存在特异性缺陷的突变体。我们发现,在发酵生长过程中,线粒体编码蛋白的表达需要多达176个核基因。综上所述,我们的数据提供了一个简单真核细胞中呼吸代谢所需分子过程的全面图景。