» Articles » PMID: 9308969

Mismatch Repair Protein MutL Becomes Limiting During Stationary-phase Mutation

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 1997 Oct 6
PMID 9308969
Citations 66
Authors
Affiliations
Soon will be listed here.
Abstract

Postsynthesis mismatch repair is an important contributor to mutation avoidance and genomic stability in bacteria, yeast, and humans. Regulation of its activity would allow organisms to regulate their ability to evolve. That mismatch repair might be down-regulated in stationary-phase Escherichia coli was suggested by the sequence spectrum of some stationary-phase ("adaptive") mutations and by the observations that MutS and MutH levels decline during stationary phase. We report that overproduction of MutL inhibits mutation in stationary phase but not during growth. MutS overproduction has no such effect, and MutL overproduction does not prevent stationary-phase decline of either MutS or MutH. These results imply that MutS and MutH decline to levels appropriate for the decreased DNA synthesis in stationary phase, whereas functional MutL is limiting for mismatch repair specifically during stationary phase. Modulation of mutation rate and genetic stability in response to environmental or developmental cues, such as stationary phase and stress, could be important in evolution, development, microbial pathogenicity, and the origins of cancer.

Citing Articles

stress-associated mutagenesis and developmental DNA repair.

Pedraza-Reyes M, Abundiz-Yanez K, Rangel-Mendoza A, Martinez L, Barajas-Ornelas R, Cuellar-Cruz M Microbiol Mol Biol Rev. 2024; 88(2):e0015823.

PMID: 38551349 PMC: 11332352. DOI: 10.1128/mmbr.00158-23.


Real-time monitoring of replication errors' fate reveals the origin and dynamics of spontaneous mutations.

Enrico Bena C, Ollion J, De Paepe M, Ventroux M, Robert L, Elez M Nat Commun. 2024; 15(1):2702.

PMID: 38538613 PMC: 10973407. DOI: 10.1038/s41467-024-46950-0.


Stress-Induced Mutagenesis, Gambler Cells, and Stealth Targeting Antibiotic-Induced Evolution.

Pribis J, Zhai Y, Hastings P, Rosenberg S mBio. 2022; 13(3):e0107422.

PMID: 35658528 PMC: 9239211. DOI: 10.1128/mbio.01074-22.


SUMO and cellular adaptive mechanisms.

Ryu H, Ahn S, Hochstrasser M Exp Mol Med. 2020; 52(6):931-939.

PMID: 32591648 PMC: 7338444. DOI: 10.1038/s12276-020-0457-2.


Regulation of the error-prone DNA polymerase Polκ by oncogenic signaling and its contribution to drug resistance.

Temprine K, Campbell N, Huang R, Langdon E, Simon-Vermot T, Mehta K Sci Signal. 2020; 13(629).

PMID: 32345725 PMC: 7428051. DOI: 10.1126/scisignal.aau1453.


References
1.
Stahl F . Bacterial genetics. A unicorn in the garden. Nature. 1988; 335(6186):112-3. DOI: 10.1038/335112a0. View

2.
Longerich S, Galloway A, Harris R, Wong C, ROSENBERG S . Adaptive mutation sequences reproduced by mismatch repair deficiency. Proc Natl Acad Sci U S A. 1995; 92(26):12017-20. PMC: 40287. DOI: 10.1073/pnas.92.26.12017. View

3.
Mellon I, Champe G . Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli. Proc Natl Acad Sci U S A. 1996; 93(3):1292-7. PMC: 40073. DOI: 10.1073/pnas.93.3.1292. View

4.
ROSENBERG S . Chain-bias of Escherichia coli Rec-mediated lambda patch recombinants is independent of the orientation of lambda cos. Genetics. 1988; 120(1):7-21. PMC: 1203507. DOI: 10.1093/genetics/120.1.7. View

5.
Galitski T, Roth J . Evidence that F plasmid transfer replication underlies apparent adaptive mutation. Science. 1995; 268(5209):421-3. DOI: 10.1126/science.7716546. View