Application of yeast cells transformed with GFP expression constructs containing the RAD54 or RNR2 promoter as a test for the genotoxic potential of chemical substances

被引:58
作者
Afanassiev, V
Sefton, M
Anantachaiyong, T
Barker, G
Walmsley, R
Wölfl, S
机构
[1] Hans Knoll Inst Nat Stoff Forsch, Abt Zell & Mol Biol, D-07745 Jena, Germany
[2] Univ Manchester, Dept Biomol Sci, Manchester M60 1QD, Lancs, England
关键词
GFP reporter; genotoxicity; MMS; DNA damage; chemical substances; yeast;
D O I
10.1016/S1383-5718(99)00209-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Yeast strains transformed with high copy number plasmids carrying the gene encoding a green fluorescent protein optimised for yeast (yEGFP3) under the control of the RAD54 or RNR2 promoter were used to investigate the activity of potentially DNA-damaging substances. The assays were performed on 96-well microtitre plates in the presence of different concentrations of the test substances. The synthesis of GFP protein was measured through the fluorescence signal and cell growth was monitored by absorption. Here, we demonstrate that this system can be used as a biosensor to assess the genotoxic potential of drugs and other chemical substances. The use of microtitre plates will enable full automation of the system and allows the inclusion of internal reference standards in each assay. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:297 / 308
页数:12
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