Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Methyl-directed DNA mismatch correction.

P Modrich1

  • 1Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710.

The Journal of Biological Chemistry
|April 25, 1989
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

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

Proceedings of the National Academy of Sciences of the United States of America·2001
Same author

Distinct MutS DNA-binding modes that are differentially modulated by ATP binding and hydrolysis.

The Journal of biological chemistry·2001
Same author

DNA chain length dependence of formation and dynamics of hMutSalpha.hMutLalpha.heteroduplex complexes.

The Journal of biological chemistry·2001
Same author

Redundant exonuclease involvement in Escherichia coli methyl-directed mismatch repair.

The Journal of biological chemistry·2001
Same author

In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

Proceedings of the National Academy of Sciences of the United States of America·2001
Same author

Somatic mutation of hPMS2 as a possible cause of sporadic human colon cancer with microsatellite instability.

Oncogene·2000
Same journal

Isotope-Edited ESEEM: A New Method for Probing Copper Binding Sites in Neurodegenerative Proteins.

The Journal of biological chemistry·2026
Same journal

YhbO is a DJ-1 family glyoxalase and α-oxoaldehyde hydratase that confers resistance to reactive carbonyl stress (112).

The Journal of biological chemistry·2026
Same journal

ARMH3 acts as a central scaffold at the Golgi/TGN through interactions with Arl5, GBF1, and PI4KB.

The Journal of biological chemistry·2026
Same journal

PAX8 controls proximal tubule epithelial identity and stress response through epigenetic modification of distal regulatory elements.

The Journal of biological chemistry·2026
Same journal

Saturated cardiolipins are potent disruptors of inner mitochondrial membrane structure and function.

The Journal of biological chemistry·2026
Same journal

Phosphate release from myosin Va occurs after the initial powerstroke but before the secondary powerstroke associated with ADP-release.

The Journal of biological chemistry·2026
See all related articles

DNA mismatch repair systems correct errors during recombination and maintain genetic stability. In Escherichia coli, multiple pathways, including the methyl-directed pathway, ensure low spontaneous mutation rates.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Robin Holliday proposed DNA mismatch correction in recombination intermediates for gene conversion in 1964.
  • Mismatch repair systems are now established in bacteria, fungi, and mammalian cells.
  • Escherichia coli possesses at least three distinct mismatch correction pathways.

Purpose of the Study:

  • To summarize the functions and mechanisms of mismatch repair systems, particularly in Escherichia coli.
  • To review the methyl-directed pathway for processing DNA biosynthetic errors and recombination intermediates.
  • To highlight the role of mismatch correction in maintaining genetic stability and low spontaneous mutability.

Main Methods:

  • Review of existing literature on mismatch repair systems in Escherichia coli and other organisms.

Related Experiment Videos

  • Focus on the methyl-directed pathway as the most extensively studied system.
  • Discussion of implicated mutator genes in E. coli mismatch repair.
  • Main Results:

    • Mismatch repair systems are crucial for processing recombination intermediates.
    • These systems significantly contribute to the genetic stability of organisms like E. coli.
    • Seven E. coli mutator genes are implicated in mismatch repair, underscoring its importance in preventing mutations.

    Conclusions:

    • Mismatch correction is vital for maintaining low spontaneous mutability.
    • The methyl-directed pathway in E. coli is a key system for DNA repair and genetic stability.
    • Further research into mismatch repair pathways across different organisms continues.