Development of a Cell-Based Assay for Measuring Base Excision Repair Responses

被引:7
|
作者
Golato, Tyler [1 ]
Brenerman, Boris [1 ]
McNeill, Daniel R. [1 ]
Li, Jianfeng [2 ]
Sobol, Robert W. [2 ]
Wilson, David M., III [1 ]
机构
[1] NIA, Lab Mol Gerontol, Intramural Res Program, NIH, 251 Bayview Blvd,Ste 100, Baltimore, MD 21224 USA
[2] Univ S Alabama, USA Mitchell Canc Inst, Mol & Metab Oncol Program, 1660 Springhill Ave, Mobile, AL 36604 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
DNA-DAMAGE REPAIR; GLYCOSYLASE; MECHANISM; MUTATION; PROTEIN; ATAXIA;
D O I
10.1038/s41598-017-12963-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Base excision repair (BER) is the predominant pathway for coping with most forms of hydrolytic, oxidative or alkylative DNA damage. Measuring BER capacity in living cells is valuable for both basic science applications and epidemiological studies, since deficiencies in this pathway have been associated with cancer susceptibility and other adverse health outcomes. At present, there is an ongoing effort to develop methods to effectively quantify the rate of BER as a whole. We present a variation of a previously described "Oligonucleotide Retrieval Assay" designed to measure DNA excision repair that is capable of quantifying the rate of repair of thymine glycol in a variety of human cells with a high degree of sensitivity.
引用
收藏
页数:13
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