Literature DB >> 11092832

DNA mismatch repair and genetic instability.

B D Harfe1, S Jinks-Robertson.   

Abstract

Mismatch repair (MMR) systems play a central role in promoting genetic stability by repairing DNA replication errors, inhibiting recombination between non-identical DNA sequences and participating in responses to DNA damage. The discovery of a link between human cancer and MMR defects has led to an explosion of research on eukaryotic MMR. The key proteins in MMR are highly conserved from bacteria to mammals, and this conservation has been critical for defining the components of eukaryotic MMR systems. In eukaryotes, there are multiple homologs of the key bacterial MutS and MutL MMR proteins, and these homologs form heterodimers that have discrete roles in MMR-related processes. This review describes the genetic and biochemical approaches used to study MMR, and summarizes the diverse roles that MMR proteins play in maintaining genetic stability.

Entities:  

Mesh:

Year:  2000        PMID: 11092832     DOI: 10.1146/annurev.genet.34.1.359

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  229 in total

1.  High rate of CAD gene amplification in human cells deficient in MLH1 or MSH6.

Authors:  S Chen; S H Bigner; P Modrich
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

2.  Isolation and characterization of point mutations in mismatch repair genes that destabilize microsatellites in yeast.

Authors:  E A Sia; M Dominska; L Stefanovic; T D Petes
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

3.  Suppression of gene amplification and chromosomal DNA integration by the DNA mismatch repair system.

Authors:  C T Lin; Y L Lyu; H Xiao; W H Lin; J Whang-Peng
Journal:  Nucleic Acids Res       Date:  2001-08-15       Impact factor: 16.971

4.  Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae.

Authors:  P T Tran; J A Simon; R M Liskay
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-31       Impact factor: 11.205

5.  Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin.

Authors:  Hideki Shimodaira; Atsuko Yoshioka-Yamashita; Richard D Kolodner; Jean Y J Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-24       Impact factor: 11.205

6.  The Escherichia coli methyl-directed mismatch repair system repairs base pairs containing oxidative lesions.

Authors:  Jennifer Wyrzykowski; Michael R Volkert
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

7.  Chloroplast DNA base substitutions: an experimental assessment.

Authors:  Monica Guhamajumdar; Barbara B Sears
Journal:  Mol Genet Genomics       Date:  2005-03-03       Impact factor: 3.291

8.  Genomic diversification among archival strains of Salmonella enterica serovar typhimurium LT7.

Authors:  Gui-Rong Liu; Kelly Edwards; Abraham Eisenstark; Ying-Mei Fu; Wei-Qiao Liu; Kenneth E Sanderson; Randal N Johnston; Shu-Lin Liu
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

9.  The effects of mismatch repair and RAD1 genes on interchromosomal crossover recombination in Saccharomyces cerevisiae.

Authors:  Ainsley Nicholson; Rebecca M Fabbri; Jason W Reeves; Gray F Crouse
Journal:  Genetics       Date:  2006-04-02       Impact factor: 4.562

10.  Transcription of a donor enhances its use during double-strand break-induced gene conversion in human cells.

Authors:  Ezra Schildkraut; Cheryl A Miller; Jac A Nickoloff
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.