Genetic polymorphisms and alternative splicing of the hOGG1 gene, that is involved in the repair of 8-hydroxyguanine in damaged DNA

被引:387
作者
Kohno, T
Shinmura, K
Tosaka, M
Tani, M
Kim, SR
Sugimura, H
Nohmi, T
Kasai, H
Yokota, J
机构
[1] Natl Canc Ctr, Res Inst, Div Biol, Chuo Ku, Tokyo 104, Japan
[2] Natl Inst Hlth Sci, Div Genet & Mutagenesis, Setagaya Ku, Tokyo 158, Japan
[3] Hamamatsu Univ Sch Med, Dept Pathol 1, Hamamatsu, Shizuoka 43131, Japan
[4] Univ Occupat & Environm Hlth, Dept Environm Oncol, Yahatanishi Ku, Kitakyushu, Fukuoka 807, Japan
关键词
8-hydroxyguanine; DNA repair; genetic polymorphism; alternative splicing; hOGG1; gene;
D O I
10.1038/sj.onc.1201872
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hOGG1 gene encodes a DNA glycosylase that excises 8-hydroxyguanine (oh(8)Gua) from damaged DNA, Structural analyses of the hOGG1 gene and its transcripts were performed in normal and lung cancer cells. Due to a genetic polymorphism at codon 326, hOGG1-Ser(326) and hOGG1-Cys(326) proteins were produced in human cells. Activity in the repair of oh8Gua was greater in hOGG1-Ser(326) protein than in hOGG1-Cys(326) protein in the complementation assay of an E, coli mutant defective in the repair of oh8Gua. Two isoforms of hOGG1 transcripts produced by alternative splicing encoded distinct hOGG1 proteins: one with and the other without a putative nuclear localization signal. Loss of heterozygosity at the hOGG1 locus was frequently (15/ 23, 62.2%) detected in lung cancer cells, and a cell Line NCI-H526 had a mutation leading to the formation of the transcripts encoding a truncated hOGG1 protein. However, the oh(8)Gua levels in nuclear DNA were similar among lung cancer cells and leukocytes irrespective of the type of hOGG1 proteins expressed. These results suggest that the oh(8)Gua levels are maintained at a steady level, even though multiple hOGG1 proteins are produced due to genetic polymorphisms, mutations and alternative splicing of the hOGG1 gene.
引用
收藏
页码:3219 / 3225
页数:7
相关论文
共 43 条
[1]  
Aburatani H, 1997, CANCER RES, V57, P2151
[2]   Cloning of a human homolog of the yeast OGG1 gene that is involved in the repair of oxidative DNA damage [J].
Arai, K ;
Morishita, K ;
Shinmura, K ;
Kohno, T ;
Kim, SR ;
Nohmi, T ;
Taniwaki, M ;
Ohwada, S ;
Yokota, J .
ONCOGENE, 1997, 14 (23) :2857-2861
[3]  
Asami S, 1996, CANCER RES, V56, P2546
[4]   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
[5]   A NOVEL ALLELIC VARIANT OF SERUM AMYLOID-A, SAA1-GAMMA - GENOMIC EVIDENCE, EVOLUTION, FREQUENCY, AND IMPLICATION AS A RISK FACTOR FOR REACTIVE SYSTEMIC AA-AMYLOIDOSIS [J].
BABA, S ;
MASAGO, SA ;
TAKAHASHI, T ;
KASAMA, T ;
SUGIMURA, H ;
TSUGANE, S ;
TSUTSUI, Y ;
SHIRASAWA, H .
HUMAN MOLECULAR GENETICS, 1995, 4 (06) :1083-1087
[6]  
BESSHO T, 1993, J BIOL CHEM, V268, P19416
[7]   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
[8]   Directing alternative splicing: Cast and scenarios [J].
Chabot, B .
TRENDS IN GENETICS, 1996, 12 (11) :472-478
[9]  
Garuti R, 1996, J LIPID RES, V37, P1459
[10]  
GAZDAR AF, 1994, ANTICANCER RES, V14, P261