Determination of hypersensitivity to genotoxic agents among Escherichia coli single gene knockout mutants

被引:16
作者
Becket, Elinne
Chen, Frank
Tamae, Cindy
Miller, Jeffrey H. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
Cisplatin; 5-Azacytidine; Zebularine; DNA METHYLATION INHIBITOR; BLEOMYCIN-INDUCED DAMAGE; DOUBLE-STRAND BREAKS; GERM-CELL TUMORS; MISMATCH REPAIR; CYTIDINE DEAMINASE; PLATINUM COMPOUNDS; DESIGN STRATEGIES; BINDING PROTEINS; OVARIAN-CANCER;
D O I
10.1016/j.dnarep.2010.06.008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have tested the KEIO collection of 3985 different viable single gene knockouts in Escherichia coli to identify genes whose loss increases sensitivity to one or more of six different chemotherapeutic agents and mutagens: Bleomycin (BLM), Cisplatin (CPT), ICR-191 (ICR), 5-azacytidine (5AZ), Zebularine (ZEB), and 5-bromo-2'-deoxyuridine (5BdU). We discovered a set of 156 strains that display a significant increase in sensitivity to at least one of the agents tested. Each genotoxic agent generates a distinct "sensitivity profile" that is characteristic of the agent. Comparison with an independent study of sensitivity profiles for an extensive set of antibiotics pinpoints those effects that are relatively specific for each agent. In some cases engineered double mutants have greatly increased effects. These results provide insight into the mechanism of action of each agent, and define targets for the design of co-drugs that can potentiate these agents. An example is the finding that mutants lacking one of several genes in the folate biosynthetic pathway are hypersensitive to ZEB, leading to a demonstration of synergy between trimethoprim and ZEB. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:949 / 957
页数:9
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