Gealy Robert, Keohavong Phouthone
Merck Research Laboratories, West Point, PA, USA.
Department of Environmental and Occupational Health, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Methods Mol Biol. 2020;2102:303-314. doi: 10.1007/978-1-0716-0223-2_17.
Polycyclic aromatic hydrocarbons (PAHs) are widely distributed in the environment and have potent mutagenic and carcinogenic activities. Studies of mutations induced by these compounds in human cells can help acquire an understanding of their mutagenic pathways. In this chapter, independent cultures of a human cell line expressing cytochrome P450 CYP1A1 (cell line MCL-5) were treated with benzo(a)pyrene (BaP) or dibenzo(a,l)pyrene (DBP), and mutants at the hypoxanthine phosphoribosyltransferase (HPRT) locus were selected en masse by 6-thioguanine resistance (6TG). The kinds and positions of the mutations occurring in the third exon of the HPRT gene were analyzed in the mixed HPRT mutant cell populations using a combination of polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE). Mutant bands were excised from the gel, amplified using PCR, and sequenced to determine the kinds and positions, or spectrum of mutations.
多环芳烃(PAHs)广泛分布于环境中,具有强大的致突变和致癌活性。对这些化合物在人类细胞中诱导的突变进行研究有助于了解其致突变途径。在本章中,用苯并(a)芘(BaP)或二苯并(a,l)芘(DBP)处理表达细胞色素P450 CYP1A1的人类细胞系(MCL-5细胞系)的独立培养物,并通过6-硫鸟嘌呤抗性(6TG)大量筛选次黄嘌呤磷酸核糖基转移酶(HPRT)位点的突变体。使用聚合酶链反应(PCR)和变性梯度凝胶电泳(DGGE)相结合的方法,在混合的HPRT突变体细胞群体中分析HPRT基因第三外显子中发生的突变的种类和位置。从凝胶中切下突变条带,用PCR扩增并测序,以确定突变的种类和位置,即突变谱。