The Shizosaccharomyces pombe homolog (SpMYH) of the Escherichia coli MutY is required for removal of guanine from 8-oxoguanine/guanine mispairs to prevent G:C to C:G transversions

被引:9
作者
Doi, T
Yonekura, SI
Tano, K
Yasuhira, S
Yonei, S
Zhang, QM
机构
[1] Kyoto Univ, Grad Sch Sci, Radiat Biol Lab, Sakyo Ku, Kyoto 6068502, Japan
[2] Kyoto Univ, Inst Res Reactor, Div Radiat Life Sci, Osaka 5900494, Japan
关键词
D O I
10.1269/jrr.46.205
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The frequency of G:C-C:G transversions significantly increases upon exposure of cells to ionizing radiation or reactive oxygen species. Transversions can be prevented by base excision repair, which removes the causative modified bases from DNA. Our previous studies revealed that MutY is responsible for removing guanine from 7,8-dihydro-8-oxoguanine/guanine mispairs (8-oxoG/G) and prevents the generation of G:C-C:G transversions in E. coli. SpMYH, a homolog of E. coli MutY, had been identified and characterized in the fission yeast S. pombe. Purified SpMYH has adenine DNA glycosylase activity on A/8-oxoG and A/G mismatch-containing oligonucleotides. In this study, we examined whether SpMYH has a similar activity allowing it to remove G from 8-oxoG/G in DNA. The purified SpMYH tightly bound to duplex oligonucleotides containing 8-oxoG/G and removed the unmodified G from 8-oxoG/G as efficiently as A from 8-oxoG/A. The activity was absent in the cell extract prepared from an SpMYH-knock-out strain of S. pombe. The expression of SpMYH markedly reduced the frequency of spontaneous G:C -> C:G transversions in the E. coli mutY mutant. These results demonstrate that SpMYH is involved in the repair of 8-oxoG/G, by which it prevents mutations induced by oxidative stress in S. pombe.
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页码:205 / 214
页数:10
相关论文
共 55 条
[1]
DNA repair and sequence context affect 1O2-induced mutagenesis in bacteria [J].
Agnez-Lima, LF ;
Napolitano, RL ;
Fuchs, RPP ;
Di Mascio, P ;
Muotri, AR ;
Menck, CFM .
NUCLEIC ACIDS RESEARCH, 2001, 29 (13) :2899-2903
[2]
HYDROGEN-PEROXIDE INDUCES G/C TO T/A AND G/C TO C/G TRANSVERSIONS IN THE SUPF GENE OF ESCHERICHIA-COLI [J].
AKASAKA, S ;
YAMAMOTO, K .
MOLECULAR & GENERAL GENETICS, 1994, 243 (05) :500-505
[3]
OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[4]
Mutagenicity, toxicity and repair of DNA base damage induced by oxidation [J].
Bjelland, S ;
Seeberg, E .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 531 (1-2) :37-80
[5]
Base excision repair of 8-hydroxyguanine protects DNA from endogenous oxidative stress [J].
Boiteux, S ;
Radicella, JP .
BIOCHIMIE, 1999, 81 (1-2) :59-67
[6]
REACTIONS OF OXYL RADICALS WITH DNA [J].
BREEN, AP ;
MURPHY, JA .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (06) :1033-1077
[7]
Hydroxyl radicals and DNA base damage [J].
Cadet, J ;
Delatour, T ;
Douki, T ;
Gasparutto, D ;
Pouget, JP ;
Ravanat, JL ;
Sauvaigo, S .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 424 (1-2) :9-21
[8]
2,2-DIAMINO-4-[(3,5-DI-O-ACETYL-2-DEOXY-BETA-D-ERYTHROPENTOFURANOSYL) AMINO]-5-(2H)-OXAZOLONE - A NOVEL AND PREDOMINANT RADICAL OXIDATION-PRODUCT OF 3',5'-DI-O-ACETYL-2'-DEOXYGUANOSINE [J].
CADET, J ;
BERGER, M ;
BUCHKO, GW ;
JOSHI, PC ;
RAOUL, S ;
RAVANAT, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (16) :7403-7404
[9]
Functional interaction of MutY homolog with proliferating cell nuclear antigen in fission yeast, Schizosaccharomyces pombe [J].
Chang, DY ;
Lu, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (14) :11853-11858
[10]
Fission yeast (Schizosaccharomyces pombe) cells defective in the MutY-homologous glycosylase activity have a mutator phenotype and are sensitive to hydrogen peroxide [J].
Chang, DY ;
Gu, Y ;
Lu, AL .
MOLECULAR GENETICS AND GENOMICS, 2001, 266 (02) :336-342