Launhardt H, Hinnen A, Munder T
Department of Cell and Molecular Biology, Hans-Knöll-Institut für Naturstoff-Forschung e. V., Jena, Germany.
Yeast. 1998 Jul;14(10):935-42. doi: 10.1002/(SICI)1097-0061(199807)14:10<935::AID-YEA289>3.0.CO;2-9.
The post-genome sequencing era of Saccharomyces cerevisiae is defined by the analysis of newly discovered open reading frames of unknown function. In this report, we describe a genetic method for the rapid identification and characterisation of genes involved in a given phenotype. This approach is based on the ability of overexpressed genomic DNA fragments to cure an induced phenotype in yeast. To validate this concept, yeast cells carrying a yeast DNA library present on multicopy plasmid vectors were screened for resistance to the antifungal drug ketoconazole. Among 1.2 million colonies 13 clones tested positive, including those expressing the lanosterol C-14 demethylase, known to be a cellular target for azole drugs, and the cytochrome-c oxidase of mitochondria, regulating the respiratory chain electron transport. Several other resistant clones were identified, which code for yeast proteins of so far unknown function. These genes may represent potential candidates for antifungal drug effects. Together with the availability of the entire yeast genome sequence, the described genetic screening method is a powerful tool for the effective functional analysis of yeast genes.
酿酒酵母的后基因组测序时代是由对新发现的功能未知的开放阅读框的分析所定义的。在本报告中,我们描述了一种用于快速鉴定和表征参与特定表型的基因的遗传方法。这种方法基于过表达的基因组DNA片段治愈酵母中诱导表型的能力。为了验证这一概念,对携带多拷贝质粒载体上的酵母DNA文库的酵母细胞进行了抗真菌药物酮康唑抗性筛选。在120万个菌落中,有13个克隆检测呈阳性,包括那些表达羊毛甾醇C-14脱甲基酶(已知是唑类药物的细胞靶点)和调节呼吸链电子传递的线粒体细胞色素c氧化酶的克隆。还鉴定出了其他几个抗性克隆,它们编码迄今功能未知的酵母蛋白。这些基因可能是抗真菌药物作用的潜在候选基因。结合整个酵母基因组序列的可用性,所描述的遗传筛选方法是对酵母基因进行有效功能分析的有力工具。