Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Methods Mol Biol. 2023;2661:281-301. doi: 10.1007/978-1-0716-3171-3_16.
Mitochondrial translation is an intricate process involving both general and mRNA-specific factors. In addition, in the yeast Saccharomyces cerevisiae, translation of mitochondrial mRNAs is coupled to assembly of nascent polypeptides into the membrane. ARG8 is a reporter gene widely used to study the mechanisms of yeast mitochondrial translation. This reporter is a recodified gene that uses the mitochondrial genetic code and is inserted at the desired locus in the mitochondrial genome. After deletion of the endogenous nuclear gene, this reporter produces Arg8, an enzyme necessary for arginine biosynthesis. Since Arg8 is a soluble protein with no relation to oxidative phosphorylation, it is a reliable reporter to study mitochondrial mRNAs translation and dissect translation form assembly processes. In this chapter, we explain how to insert the ARG8 reporter in the desired spot in the mitochondrial DNA, how to analyze Arg8 synthesis inside mitochondria, and how to follow steady-state levels of the protein. We also explain how to use it to find spontaneous suppressors of translation defects.
线粒体翻译是一个复杂的过程,涉及通用和 mRNA 特异性因子。此外,在酵母酿酒酵母中,线粒体 mRNA 的翻译与新生多肽组装到膜中相偶联。ARG8 是一种广泛用于研究酵母线粒体翻译机制的报告基因。该报告基因是一种重新编码的基因,使用线粒体遗传密码,并插入线粒体基因组中所需的基因座。在删除内源性核基因后,该报告基因产生 Arg8,这是精氨酸生物合成所必需的酶。由于 Arg8 是一种与氧化磷酸化无关的可溶性蛋白,因此它是研究线粒体 mRNA 翻译和剖析翻译形式组装过程的可靠报告基因。在本章中,我们将解释如何将 ARG8 报告基因插入线粒体 DNA 中的所需位置,如何分析线粒体内部的 Arg8 合成,以及如何跟踪蛋白质的稳态水平。我们还解释如何使用它来寻找翻译缺陷的自发抑制因子。