Functional mutation of DNA polymerase β found in human gastric cancer -: inability of the base excision repair in vitro

被引:63
作者
Iwanaga, A
Ouchida, M
Miyazaki, K
Hori, K
Mukai, T
机构
[1] Saga Med Sch, Dept Biochem, Saga, Japan
[2] Saga Med Sch, Dept Surg, Saga, Japan
[3] Okayama Univ, Inst Cellular & Mol Biol, Dept Mol Genet, Okayama, Japan
来源
MUTATION RESEARCH-DNA REPAIR | 1999年 / 435卷 / 02期
关键词
DNA polymerase beta; mutation; base excision repair; gastric cancer;
D O I
10.1016/S0921-8777(99)00036-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
DNA polymerase beta (pol beta) is one of mammalian DNA polymerases and is known to be involved in a G:T/G:U mismatch repair. In order to investigate an involvement of this enzyme in a base excision repair, we searched a mutation of human pol beta in human gastric cancer and studied a function of the mutation. We observed cancer-specific missense mutations in 6 of 20 samples. All of these mutations were, however, heterozygous. We further analyzed the base excision repair activity of these mutants to know whether these mutants cause an error of mismatch repair. One of these mutants, which resulted in an amino acid substitution of Glu for Lys at codon 295, showed an inhibitory effect by in vitro base excision repair assay, suggesting that this mutation might play some role in carcinogenesis of the gastric mucosa. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:121 / 128
页数:8
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