Muenter Mark M, Aiken Ariel, Akanji Jadesola O, Baig Samir, Bellou Sirine, Carlson Alyssa, Conway Charles, Cowell Courtney M, DeLateur Nicholas A, Hester Alexis, Joshi Christopher, Kramer Caitlin, Leifer Becky S, Nash Emma, Qi Macee H, Travers Meghan, Wong Kelly C, Hu Man, Gou Na, Giese Roger W, Gu April Z, Beuning Penny J
Department of Chemistry & Chemical Biology, Northeastern University, Boston, MA, 02115 USA.
Department of Civil and Environmental Engineering, Northeastern University, Boston, MA, 02115 USA.
Mutat Res Genet Toxicol Environ Mutagen. 2019 Apr;840:1-10. doi: 10.1016/j.mrgentox.2019.02.001. Epub 2019 Feb 7.
DNA damage is ubiquitous and can arise from endogenous or exogenous sources. DNA-damaging alkylating agents are present in environmental toxicants as well as in cancer chemotherapy drugs and are a constant threat, which can lead to mutations or cell death. All organisms have multiple DNA repair and DNA damage tolerance pathways to resist the potentially negative effects of exposure to alkylating agents. In bacteria, many of the genes in these pathways are regulated as part of the SOS reponse or the adaptive response. In this work, we probed the cellular responses to the alkylating agents chloroacetaldehyde (CAA), which is a metabolite of 1,2-dichloroethane used to produce polyvinyl chloride, and styrene oxide (SO), a major metabolite of styrene used in the production of polystyrene and other polymers. Vinyl chloride and styrene are produced on an industrial scale of billions of kilograms annually and thus have a high potential for environmental exposure. To identify stress response genes in E. coli that are responsible for tolerance to the reactive metabolites CAA and SO, we used libraries of transcriptional reporters and gene deletion strains. In response to both alkylating agents, genes associated with several different stress pathways were upregulated, including protein, membrane, and oxidative stress, as well as DNA damage. E. coli strains lacking genes involved in base excision repair and nucleotide excision repair were sensitive to SO, whereas strains lacking recA and the SOS gene ybfE were sensitive to both alkylating agents tested. This work indicates the varied systems involved in cellular responses to alkylating agents, and highlights the specific DNA repair genes involved in the responses.
DNA损伤普遍存在,可源自内源性或外源性。DNA损伤性烷基化剂存在于环境毒物以及癌症化疗药物中,是一种持续的威胁,可导致突变或细胞死亡。所有生物体都有多种DNA修复和DNA损伤耐受途径来抵抗接触烷基化剂的潜在负面影响。在细菌中,这些途径中的许多基因作为SOS反应或适应性反应的一部分受到调控。在这项研究中,我们探究了细胞对烷基化剂氯乙醛(CAA)和环氧苯乙烯(SO)的反应,CAA是用于生产聚氯乙烯的1,2 - 二氯乙烷的代谢产物,SO是用于生产聚苯乙烯和其他聚合物的苯乙烯的主要代谢产物。氯乙烯和苯乙烯的年产量达到数十亿公斤的工业规模,因此具有很高的环境暴露可能性。为了鉴定大肠杆菌中负责耐受活性代谢产物CAA和SO的应激反应基因,我们使用了转录报告基因文库和基因缺失菌株。针对这两种烷基化剂,与几种不同应激途径相关的基因被上调,包括蛋白质、膜和氧化应激以及DNA损伤。缺乏参与碱基切除修复和核苷酸切除修复基因的大肠杆菌菌株对SO敏感,而缺乏recA和SOS基因ybfE的菌株对所测试的两种烷基化剂均敏感。这项工作表明了细胞对烷基化剂反应中涉及的多种系统,并突出了反应中涉及的特定DNA修复基因。