THE INDUCTION OF ADAPTIVE RESPONSE TO ALKYLATING-AGENTS IN ESCHERICHIA-COLI REDUCES THE FREQUENCY OF SPECIFIC C-]T MUTATIONS IN CHLOROACETALDEHYDE-TREATED M13 GLYU PHAGE

被引:11
作者
BORYS, E [1 ]
MROCZKOWSKASLUPSKA, MM [1 ]
KUSMIEREK, JT [1 ]
机构
[1] POLISH ACAD SCI,INST BIOCHEM & BIOPHYS,PL-02532 WARSAW,POLAND
关键词
D O I
10.1093/mutage/9.5.407
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mutagenicity and repair of cytosine adducts formed in reactions of chloroacetaldehyde (CAA), a metabolite of the human carcinogen vinyl chloride, have been studied. The treatment of single-stranded DNA M13 JCM15472 (glyU313) phage with CAA and subsequent transfection of Escherichia coli K-12 JC15419 (trpA461) tester strain resulted in a dose-dependent increase of phage C --> T transitions and a decrease of phage survival. The induction of the adaptive response to alkylating agents in bacterial cells significantly decreased the frequency of examined C --> T transitions and increased phage survival. The results indicate that both CAA adducts to cytosine, the initially formed 3,N-4-(N-4-alpha-hydroxyethano)cytosine and the product of its dehydration, 3,N-4-ethenocytosine, provoke C --> T transitions and are repaired in adapted bacteria. The role of 3-methyladenine-DNA glycosylase II, which is a part of the adaptive response system in E.coli, in excision of CAA adducts to cytosine, is discussed.
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页码:407 / 410
页数:4
相关论文
共 19 条
[1]   INDUCTION OF SPECIFIC BASE-PAIR SUBSTITUTIONS IN ESCHERICHIA-COLI TRPA MUTANTS BY CHLOROETHYLENE OXIDE, A CARCINOGENIC VINYL-CHLORIDE METABOLITE [J].
BARBIN, A ;
BESSON, F ;
PERRARD, MH ;
BEREZIAT, JC ;
KALDOR, J ;
MICHEL, G ;
BARTSCH, H .
MUTATION RESEARCH, 1985, 152 (2-3) :147-156
[2]   GENETIC-ANALYSIS OF UV MUTAGENESIS OF THE ESCHERICHIA-COLI GLYU GENE [J].
CIESLA, Z ;
OBRIEN, P ;
CLARK, AJ .
MOLECULAR & GENERAL GENETICS, 1987, 207 (01) :1-8
[3]   ALL 4 KNOWN CYCLIC ADDUCTS FORMED IN DNA BY THE VINYL-CHLORIDE METABOLITE CHLOROACETALDEHYDE ARE RELEASED BY A HUMAN DNA GLYCOSYLASE [J].
DOSANJH, MK ;
CHENNA, A ;
KIM, E ;
FRAENKELCONRAT, H ;
SAMSON, L ;
SINGER, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (03) :1024-1028
[4]  
GREEN T, 1990, ANNU REV PHARMACOL, V30, P73
[5]  
GUENGERICH PF, 1992, J AM CHEM SOC, V3, P1074
[6]  
JACOBSEN JS, 1989, GENETICS, V121, P213
[7]   SYNTHESIS OF N2,3-ETHENODEOXYGUANOSINE, N2,3-ETHENODEOXYGUANOSINE 5'-PHOSPHATE, AND N2,3-ETHENODEOXYGUANOSINE 5'-TRIPHOSPHATE - STABILITY OF THE GLYCOSYL BOND IN THE MONOMER AND IN POLY(DG, EPSILON-DG-DC) [J].
KUSMIEREK, JT ;
FOLKMAN, W ;
SINGER, B .
CHEMICAL RESEARCH IN TOXICOLOGY, 1989, 2 (04) :230-233
[8]   1,N-2-ETHENODEOXYGUANOSINE - PROPERTIES AND FORMATION IN CHLOROACETALDEHYDE-TREATED POLYNUCLEOTIDES AND DNA [J].
KUSMIEREK, JT ;
SINGER, B .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (05) :634-638
[9]   CHLOROACETALDEHYDE-TREATED RIBOPOLYNUCLEOTIDE AND DEOXYRIBOPOLYNUCLEOTIDE .2. ERRORS IN TRANSCRIPTION BY DIFFERENT POLYMERASES RESULTING FROM ETHENOCYTOSINE AND ITS HYDRATED INTERMEDIATE [J].
KUSMIEREK, JT ;
SINGER, B .
BIOCHEMISTRY, 1982, 21 (22) :5723-5728
[10]   CHLOROACETALDEHYDE-TREATED RIBOPOLYNUCLEOTIDE AND DEOXYRIBOPOLYNUCLEOTIDE .1. REACTION-PRODUCTS [J].
KUSMIEREK, JT ;
SINGER, B .
BIOCHEMISTRY, 1982, 21 (22) :5717-5722