Interactions among the Escherichia coli mutT, mutM, and mutY damage prevention pathways

被引:98
作者
Fowler, RG [1 ]
White, SJ
Koyama, C
Moore, SC
Dunn, RL
Schaaper, RM
机构
[1] San Jose State Univ, Dept Biol Sci, San Jose, CA 95192 USA
[2] NIEHS, Mol Genet Lab, Res Triangle Pk, NC 27709 USA
关键词
oxidation damage; 8-oxodGTP; 8-oxoguanine; mutators; spontaneous mutations;
D O I
10.1016/S1568-7864(02)00193-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have investigated in detail the interactions between the Escherichia coli mutT, mutM, and mutY error-prevention systems. Jointly, these systems protect the cell against the effects of the oxidative stress product, 8-oxoguanine (8-oxoG), a base analog with ambiguous base-pairing properties, pairing with either A or C during DNA synthesis. mutT mutator strains display a specific increase in A.T --> C.G transversions, while mutM and mutY mutator strains show specific G.C --> T.A increases. To study in more detail the in vivo processing of the various mutational intermediates leading to A.T --> C.G and G.C --> T.A transversions, we analyzed defined A.T --> C.G and G.C --> T.A events in strains containing all possible combinations of these mutator alleles. We report three major findings. First, we do not find evidence that the mutT allele significantly increases G.C --> T.A transversions in either mut(+), mutM, mutY or mutMmutY backgrounds. We interpret this result to indicate that incorporation of 8-oxodGTP opposite template C may not be frequent relative to incorporation opposite template A. Second, we show that mutT-induced A.T --> C.G transversions are significantly reduced in strains carrying mutY and mutMmutY deficiencies suggesting that 8-oxoG, when present in DNA, preferentially mispairs with dATP. Third, the mutY and mutMmutY deficiencies also decrease A.T --> C.G transversions in the muT(+) background, suggesting that, even in the presence of functional MutT protein, A.T --> C.G transversions may still result from 8-oxodGTP misincorporation. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:159 / 173
页数:15
相关论文
共 61 条
[1]  
ALLEN MK, 1963, GENETICS, V48, P1065
[2]   ESCHERICHIA-COLI MUTY GENE ENCODES AN ADENINE GLYCOSYLASE ACTIVE ON G-A MISPAIRS [J].
AU, KG ;
CLARK, S ;
MILLER, JH ;
MODRICH, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8877-8881
[3]   The base substitution fidelity of HIV-1 reverse transcriptase on DNA and RNA templates probed with 8-oxo-deoxyguanosine triphosphate [J].
Bebenek, K ;
Boyer, JC ;
Kunkel, TA .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 429 (02) :149-158
[4]   A novel role for Escherichia coli endonuclease VIII in prevention of spontaneous G→T transversions [J].
Blaisdell, JO ;
Hatahet, Z ;
Wallace, SS .
JOURNAL OF BACTERIOLOGY, 1999, 181 (20) :6396-6402
[5]   SUBSTRATE-SPECIFICITY OF THE ESCHERICHIA-COLI FPG PROTEIN (FORMAMIDOPYRIMIDINE DNA GLYCOSYLASE) - EXCISION OF PURINE LESIONS IN DNA PRODUCED BY IONIZING-RADIATION OR PHOTOSENSITIZATION [J].
BOITEUX, S ;
GAJEWSKI, E ;
LAVAL, J ;
DIZDAROGLU, M .
BIOCHEMISTRY, 1992, 31 (01) :106-110
[6]   MUTM, A 2ND MUTATOR LOCUS IN ESCHERICHIA-COLI THAT GENERATES G.C-]T.A TRANSVERSIONS [J].
CABRERA, M ;
NGHIEM, Y ;
MILLER, JH .
JOURNAL OF BACTERIOLOGY, 1988, 170 (11) :5405-5407
[7]  
CHENG KC, 1992, J BIOL CHEM, V267, P166
[8]   PURIFICATION AND CHARACTERIZATION OF ESCHERICHIA-COLI FORMAMIDOPYRIMIDINE-DNA GLYCOSYLASE THAT EXCISES DAMAGED 7-METHYLGUANINE FROM DEOXYRIBONUCLEIC-ACID [J].
CHETSANGA, CJ ;
LOZON, M ;
MAKAROFF, C ;
SAVAGE, L .
BIOCHEMISTRY, 1981, 20 (18) :5201-5207
[9]   AN ENDONUCLEASE ACTIVITY OF ESCHERICHIA-COLI THAT SPECIFICALLY REMOVES 8-HYDROXYGUANINE RESIDUES FROM DNA [J].
CHUNG, MH ;
KASAI, H ;
JONES, DS ;
INOUE, H ;
ISHIKAWA, H ;
OHTSUKA, E ;
NISHIMURA, S .
MUTATION RESEARCH, 1991, 254 (01) :1-12
[10]   The mammalian mismatch repair pathway removes DNA 8-oxodGMP incorporated from the oxidized dNTP pool [J].
Colussi, C ;
Parlanti, E ;
Degan, P ;
Aquilina, G ;
Barnes, D ;
Macpherson, P ;
Karran, P ;
Crescenzi, M ;
Dogliotti, E ;
Bignami, M .
CURRENT BIOLOGY, 2002, 12 (11) :912-918