Analysis of gene-specific DNA damage and repair using quantitative polymerase chain reaction

被引:189
作者
Ayala-Torres, S
Chen, YM
Svoboda, T
Rosenblatt, J
Van Houten, B
机构
[1] Univ Texas, Med Branch, Sealy Ctr Mol Sci, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Div Biomath, Galveston, TX 77555 USA
[3] Shriners Burns Inst, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1006/meth.2000.1054
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Soon after discovery of the polymerase chain reaction (PCR), various laboratories have attempted to use quantitative PCR (QPCR) to detect DNA damage in specific gene segments. The development of techniques that facilitate long PCR increased the sensitivity of the assay so that biologically relevant doses of DNA-damaging agents could be assessed. QPCR has been used to survey DNA damage induced by different genotoxicants and to establish the repair kinetics of numerous genes. Current work seeks to analyze damage and repair in specific genes from animals exposed to specific DNA-damaging agents such as oxidative stress. (C) 2000 Academic Press.
引用
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页码:135 / 147
页数:13
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