Author:
Dai Da-Peng,Gan Wei,Hayakawa Hiroshi,Zhu Jia-Lou,Zhang Xiu-Qing,Hu Guo-Xin,Xu Tao,Jiang Zhe-Li,Zhang Li-Qun,Hu Xue-Da,Nie Ben,Zhou Yue,Li Jin,Zhou Xiao-Yang,Li Jian,Zhang Tie-Mei,He Qing,Liu Dong-Ge,Chen Hai-Bo,Yang Nan,Zuo Ping-Ping,Zhang Zhi-Xin,Yang Huan-Ming,Wang Yao,Wilson Samuel H.,Zeng Yi-Xin,Wang Jian-Ye,Sekiguchi Mutsuo,Cai Jian-Ping
Abstract
Reactive oxygen species formed within the mammalian cell can produce 8-oxo-7,8-dihydroguanine (8-oxoG) in mRNA, which can cause base mispairing during gene expression. Here we found that administration of 8-oxoGTP in MTH1-knockdown cells results in increased 8-oxoG content in mRNA. Under this condition, an amber mutation of the reporter luciferase is suppressed. Using second-generation sequencing techniques, we found that U-to-G changes at preassigned sites of the luciferase transcript increased when 8-oxoGTP was supplied. In addition, an increased level of 8-oxoG content in RNA induced the accumulation of aggregable amyloid β peptides in cells expressing amyloid precursor protein. Our findings indicate that 8-oxoG accumulation in mRNA can alter protein synthesis in mammalian cells. Further work is required to assess the significance of these findings under normal physiological conditions.
Funder
Key International Science and Technology Cooperation Project of China
National Natural Science Foundation of China
Intramural Research Program of the National Institues of Health, NIEHS
Publisher
Proceedings of the National Academy of Sciences
Cited by
57 articles.
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