Analysis of DNA mismatch repair activity in live cells
Loss of DNA mismatch repair (MMR) function leads to the development and progression of certain cancers. Currently, assays for DNA MMR activity involve the use of cell extracts and are technically challenging and costly. In this study, we develop a convenient spectrometric assay system for specific and quantitative measurement of DNA mismatch repair activity intracellularly. A G-T mismatch was introduced to the upstream region of firefly luciferase coding sequence in the pGL3-Control plasmid. Only if the G:T mismatches were repaired to G:C, will luciferase be expressed in transfected cells. By measuring luciferase activity, it is simple and convenient to assay intracellular DNA mismatch repair activity.
DNA mismatch repair intracellular luciferase
Li Shiying Zhang Xin Qiu Fan Hua Zi-Chun
The State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, 210093, China
国际会议
南京
英文
46-50
2010-05-12(万方平台首次上网日期,不代表论文的发表时间)