Molecular Genetics Laboratory, Division of Bioscience and Biotechnology, Department of Environmental and Life Sciences, Toyohashi University of Technology, 1-1 Hibarigaoka, Tempaku-cho, Toyohashi, Aichi, 441-8580, Japan.
Appl Microbiol Biotechnol. 2018 Mar;102(6):2493-2507. doi: 10.1007/s00253-018-8783-1. Epub 2018 Feb 8.
By damaging DNA molecules, genotoxicants cause genetic mutations and also increase human susceptibility to cancers and genetic diseases. Over the past four decades, several assays have been developed in the budding yeast Saccharomyces cerevisiae to screen potential genotoxic substances and provide alternatives to animal-based genotoxicity tests. These yeast-based genotoxicity tests are either DNA alteration-based or DNA stress-response reporter-based. The former, which came first, were developed from the genetic studies conducted on various types of DNA alterations in yeast cells. Despite their limited throughput capabilities, some of these tests have been used as short-term genotoxicity tests in addition to bacteria- or mammalian cell-based tests. In contrast, the latter tests are based on the emergent transcriptional induction of DNA repair-related genes via activation of the DNA damage checkpoint kinase cascade triggered by DNA damage. Some of these reporter assays have been linked to DNA damage-responsive promoters to assess chemical carcinogenicity and ecotoxicity in environmental samples. Yeast-mediated genotoxicity tests are being continuously improved by increasing the permeability of yeast cell walls, by the ectopic expression of mammalian cytochrome P450 systems, by the use of DNA repair-deficient host strains, and by integrating them into high-throughput formats or microfluidic devices. Notably, yeast-based reporter assays linked with the newer toxicogenomic approaches are becoming powerful short-term genotoxicity tests for large numbers of compounds. These tests can also be used to detect polluted environmental samples, and as effective screening tools during anticancer drug development.
通过破坏 DNA 分子,遗传毒性物质会导致基因突变,并增加人类患癌症和遗传疾病的易感性。在过去的四十年中,已经在新兴酵母酿酒酵母中开发了几种测定法,以筛选潜在的遗传毒性物质,并提供替代动物遗传毒性测试的方法。这些基于酵母的遗传毒性测试要么基于 DNA 改变,要么基于 DNA 应激反应报告基因。前者首先从酵母细胞中各种类型的 DNA 改变的遗传研究中发展而来。尽管它们的通量能力有限,但其中一些测试除了细菌或哺乳动物细胞测试外,还被用作短期遗传毒性测试。相比之下,后者测试是基于通过 DNA 损伤检查点激酶级联的激活,对与 DNA 修复相关的基因进行转录诱导,从而引发 DNA 应激反应。其中一些报告基因测定法已与 DNA 损伤响应启动子相关联,以评估环境样品中的化学致癌性和生态毒性。通过增加酵母细胞壁的通透性、异位表达哺乳动物细胞色素 P450 系统、使用 DNA 修复缺陷型宿主菌株,以及将其整合到高通量格式或微流控设备中,酵母介导的遗传毒性测试正在不断得到改进。值得注意的是,与较新的毒理基因组学方法相关的基于酵母的报告基因测定法正在成为大量化合物的强大短期遗传毒性测试方法。这些测试还可用于检测污染的环境样品,并在抗癌药物开发过程中用作有效的筛选工具。