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OGG1 is essential in oxidative stress induced DNA demethylation
被引:72
|作者:
Zhou, Xiaolong
[1
]
Zhuang, Ziheng
[2
,3
]
Wang, Wentao
[1
]
He, Lingfeng
[1
]
Wu, Huan
[1
]
Cao, Yan
[1
]
Pan, Feiyan
[1
]
Zhao, Jing
[1
]
Hu, Zhigang
[1
]
Sekhar, Chandra
[1
]
Guo, Zhigang
[1
]
机构:
[1] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Mol & Med Biotechnol, 1 WenYuan Rd, Nanjing 210023, Jiangsu, Peoples R China
[2] Changzhou 7 Peoples Hosp, Changzhou 213011, Peoples R China
[3] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou 213011, Peoples R China
基金:
高等学校博士学科点专项科研基金;
中国国家自然科学基金;
关键词:
DNA demethylation;
Oxidative stress;
OGG1;
TET1;
8-OxoG;
BASE EXCISION-REPAIR;
CPG-ISLAND METHYLATION;
GENE-EXPRESSION;
THYMINE GLYCOL;
GLYCOSYLASE;
8-OXOGUANINE;
DAMAGE;
TET1;
8-HYDROXYGUANINE;
TRANSCRIPTION;
D O I:
10.1016/j.cellsig.2016.05.021
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
DNA demethylation is an essential cellular activity to regulate gene expression; however, the mechanism that triggers DNA demethylation remains unknown. Furthermore, DNA demethylation was recently demonstrated to be induced by oxidative stress without a clear molecular mechanism. In this manuscript, we demonstrated that 8-oxoguanine DNA glycosylase-1 (OGG1) is the essential protein involved in oxidative stress-induced DNA demethylation. Oxidative stress induced the formation of 8-oxoguanine (8-oxoG). We found that OGG1, the 8-oxoG binding protein, promotes DNA demethylation by interacting and recruiting TET1 to the 8-oxoG lesion. Downregulation of OGG1 makes cells resistant to oxidative stress-induced DNA demethylation, while over-expression of OGG1 renders cells susceptible to DNA demethylation by oxidative stress. These data not only illustrate the importance of base excision repair (BER) in DNA demethylation but also reveal how the DNA demethylation signal is transferred to downstream DNA demethylation enzymes. (C) 2016 Elsevier Inc. All rights reserved.
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页码:1163 / 1171
页数:9
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