This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hong, E. S.
Right arrow Articles by Miller, J. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hong, E. S.
Right arrow Articles by Miller, J. H.

 Previous Article  |  Next Article 

Journal of Bacteriology, February 2005, p. 840-846, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.840-846.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Mutants with Temperature-Sensitive Defects in the Escherichia coli Mismatch Repair System: Sensitivity to Mispairs Generated In Vivo

Esther S. Hong,1 Annie Yeung,1 Pauline Funchain,1 Malgorzata M. Slupska,1,{dagger} and Jeffrey H. Miller1*

Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, California1

Received 17 August 2004/ Accepted 20 October 2004

We have used direct selections to generate large numbers of mutants of Escherichia coli defective in the mismatch repair system and have screened these to identify mutants with temperature-sensitive defects. We detected and sequenced mutations that give rise to temperature-sensitive MutS, MutL, and MutH proteins. One mutation, mutS60, results in almost normal levels of spontaneous mutations at 37°C but above this temperature gives rise to higher and higher levels of mutations, reaching the level of null mutations in mutS at 43°C. However, at 37°C the MutS60 protein can be much more easily titrated by mispairs than the wild-type MutS, as evidenced by the impaired ability to block homeologous recombination in interspecies crosses and the increased levels of mutations from weak mutator alleles of mutD (dnaQ), mutC, and ndk. Strains with mutS60 can detect mispairs generated during replication that lead to mutation with much greater sensitivity than wild-type strains. The findings with ndk, lacking nucleotide diphosphate kinase, are striking. An ndk mutS60 strain yields four to five times the level of mutations seen in a full knockout of mutS. These results pose the question of whether similar altered Msh2 proteins result from presumed polymorphisms detected in tumor lines. The role of allele interactions in human disease susceptibility is discussed.


* Corresponding author. Mailing address: Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, CA 90095. Phone: (310) 825-8460. Fax: (310) 206-3088. E-mail: jhmiller{at}mbi.ucla.edu.

{dagger} Present address: Diversa, San Diego, CA 92121.


Journal of Bacteriology, February 2005, p. 840-846, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.840-846.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.