AluYb8 insertion in the MUTYH gene is related to increased 8-OHdG in genomic DNA and could be a risk factor for type 2 diabetes in a Chinese population

被引:15
作者
Chen, Huimei [2 ,5 ]
Sun, Caixia [2 ,5 ]
Guo, Wenwen [2 ,5 ]
Meng, Ran [2 ,5 ]
Du, Hong [3 ]
Qi, Qiufeng [2 ,5 ]
Gu, Xin [2 ,5 ]
Li, Lirong [1 ]
Zhang, Kui [4 ]
Zhu, Dalong [1 ]
Wang, Yaping [2 ,5 ]
机构
[1] Nanjing Univ, Dept Endocrinol, Sch Med, Affiliated Drum Tower Hosp, Nanjing 210008, Peoples R China
[2] Nanjing Univ, Dept Med Genet, Sch Med, Nanjing 210093, Peoples R China
[3] Nanjing Univ, Sch Med, Jinling Hosp, Res Inst Endocrinol, Nanjing, Peoples R China
[4] Nanjing Univ, Lab Clin Biochem, Sch Med, Affiliated Drum Tower Hosp, Nanjing, Peoples R China
[5] Nanjing Univ, Jiangsu Key Lab Mol Med, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
MUTYH gene; 8-OHdG; Association study; Type 2 diabetes mellitus; Gene polymorphism; OXIDATIVE STRESS; REPAIR ENZYME; DAMAGE; EXCISION; 8-HYDROXYGUANINE; INACTIVATION; MUTATIONS; MECHANISM; MYH;
D O I
10.1016/j.mce.2010.11.021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Mutyh DNA glycosylase is involved in the repair of oxidized DNA bases. Because oxidative stress may contribute to increased diabetes risk, the common variant of the MUTYH gene (AluYb8MUTYH) was investigated for its possible role in type 2 diabetes mellitus (T2DM). A total of 565 T2DM patients and 565 healthy subjects from China were enrolled in a case-control study. The distribution of AluYb8MUTYH differed in diabetic patients from controls, with a moderately increased percentage of the mutant allele (P) (44.7% versus 40.3%, P= 0.033,OR = 1.199). However, this distribution was similar between the diabetic early-onset and late-onset subgroups. Another 66 T2DM patients were further evaluated for 8-hydroxy-2'deoxyguanosine (8-OHdG) levels in leukocytic DNA. The average value of 8-OHdG/10(6) dG was 10.4 in patients with the wild-type genotype, 15.9 in heterozygotes, and 22.3 in homozygotes with the variation (P < 0.001, compared with the wild-type). Therefore, the AluYb8MUTYH polymorphism could be a novel genetic risk factor for T2DM, and accumulated 8-OHdG could contribute to this disease. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:301 / 305
页数:5
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