Gu Liya, Li Guo-Min
Department of Toxicology and Pathology, University of Kentucky Medical Center, Lexington, USA.
Methods Enzymol. 2006;408:303-17. doi: 10.1016/S0076-6879(06)08019-0.
Significant advances have been made in identifying and characterizing the roles of DNA mismatch repair (MMR) proteins in cellular response to DNA damage. Insights into this process have been obtained by performing interactions of mismatch recognition proteins (e.g., MutSalpha) with DNA adduct-containing duplexes and by analyzing cellular responses (including cell cycle checkpoints and apoptosis) of cell lines and animals with various MMR capacities. This chapter presents detailed methods for gel-shift analysis to determine the interaction between MutSalpha and oligonucleotide duplex containing a single DNA adduct and for apoptotic assays in cell lines and experimental animals. In addition, a step-by-step protocol is also provided for the purification of MutSalpha from human cells, the preparation of DNA substrates containing a defined DNA adduct, and the treatment of MMR-proficient and deficient cell lines as well as MMR knockout mice.
在识别和表征DNA错配修复(MMR)蛋白在细胞对DNA损伤反应中的作用方面已取得了重大进展。通过使错配识别蛋白(如MutSα)与含DNA加合物的双链体相互作用,以及分析具有不同MMR能力的细胞系和动物的细胞反应(包括细胞周期检查点和细胞凋亡),对这一过程有了深入了解。本章介绍了用于凝胶迁移分析以确定MutSα与含单个DNA加合物的寡核苷酸双链体之间相互作用的详细方法,以及用于细胞系和实验动物凋亡检测的详细方法。此外,还提供了从人细胞中纯化MutSα、制备含特定DNA加合物的DNA底物,以及处理MMR功能正常和缺陷的细胞系以及MMR基因敲除小鼠的分步方案。