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
[31]   MUTT PROTEIN SPECIFICALLY HYDROLYZES A POTENT MUTAGENIC SUBSTRATE FOR DNA-SYNTHESIS [J].
MAKI, H ;
SEKIGUCHI, M .
NATURE, 1992, 355 (6357) :273-275
[32]   Activation of human MutS homologs by 8-oxo-guanine DNA damage [J].
Mazurek, A ;
Berardini, M ;
Fishel, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8260-8266
[33]   CRYSTAL-STRUCTURE OF A DNA DUPLEX CONTAINING 8-HYDROXYDEOXYGUANINE-ADENINE BASE-PAIRS [J].
MCAULEYHECHT, KE ;
LEONARD, GA ;
GIBSON, NJ ;
THOMSON, JB ;
WATSON, WP ;
HUNTER, WN ;
BROWN, T .
BIOCHEMISTRY, 1994, 33 (34) :10266-10270
[34]   A REPAIR SYSTEM FOR 8-OXO-7,8-DIHYDRODEOXYGUANINE [J].
MICHAELS, ML ;
TCHOU, J ;
GROLLMAN, AP ;
MILLER, JH .
BIOCHEMISTRY, 1992, 31 (45) :10964-10968
[35]   THE GO SYSTEM PROTECTS ORGANISMS FROM THE MUTAGENIC EFFECT OF THE SPONTANEOUS LESION 8-HYDROXYGUANINE (7,8-DIHYDRO-8-OXOGUANINE) [J].
MICHAELS, ML ;
MILLER, JH .
JOURNAL OF BACTERIOLOGY, 1992, 174 (20) :6321-6325
[36]   MUTM, A PROTEIN THAT PREVENTS G.C-]T.A TRANSVERSIONS, IS FORMAMIDOPYRIMIDINE-DNA GLYCOSYLASE [J].
MICHAELS, ML ;
PHAM, L ;
CRUZ, C ;
MILLER, JH .
NUCLEIC ACIDS RESEARCH, 1991, 19 (13) :3629-3632
[37]  
MICHAELS ML, 1992, P NATL ACAD SCI USA, V89, P70212
[38]   8-OxodGTP incorporation by DNA polymerase β is modified by active-site residue Asn279 [J].
Miller, H ;
Prasad, R ;
Wilson, SH ;
Johnson, F ;
Grollman, AP .
BIOCHEMISTRY, 2000, 39 (05) :1029-1033
[39]   THE MUTY GENE - A MUTATOR LOCUS IN ESCHERICHIA-COLI THAT GENERATES G.C-]T.A TRANSVERSIONS [J].
NGHIEM, Y ;
CABRERA, M ;
CUPPLES, CG ;
MILLER, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2709-2713
[40]   MSH2 and MSH6 are required for removal of adenine misincorporated opposite 8-oxo-guanine in S-cerevisiae [J].
Ni, TT ;
Marsischky, GT ;
Kolodner, RD .
MOLECULAR CELL, 1999, 4 (03) :439-444