Literature DB >> 16793377

Analysis of DNA mismatch repair in cellular response to DNA damage.

Liya Gu1, Guo-Min Li.   

Abstract

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.

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Year:  2006        PMID: 16793377     DOI: 10.1016/S0076-6879(06)08019-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  3 in total

1.  Distinct nucleotide binding/hydrolysis properties and molar ratio of MutSalpha and MutSbeta determine their differential mismatch binding activities.

Authors:  Lei Tian; Liya Gu; Guo-Min Li
Journal:  J Biol Chem       Date:  2009-02-19       Impact factor: 5.157

2.  Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells.

Authors:  Feng Li; Lei Tian; Liya Gu; Guo-Min Li
Journal:  J Biol Chem       Date:  2009-10-05       Impact factor: 5.157

3.  Mispair-bound human MutS-MutL complex triggers DNA incisions and activates mismatch repair.

Authors:  Janice Ortega; Grace Sanghee Lee; Liya Gu; Wei Yang; Guo-Min Li
Journal:  Cell Res       Date:  2021-01-28       Impact factor: 46.297

  3 in total

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