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

RMPs: recombination/replication mediator proteins.

H T Beernink1, S W Morrical

  • 1Dept of Biochemistry and Center for X-ray Crystallography, The University of Vermont College of Medicine, Burlington, VT 05405-0068, USA.

Trends in Biochemical Sciences
|September 29, 1999
PubMed
Summary

Recombination/replication mediator proteins (RMPs) help DNA replication and recombination enzymes access single-stranded DNA (ssDNA). These specialized proteins overcome inhibition by single-stranded DNA-binding proteins (SSBs), facilitating crucial DNA processes.

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

Mediator proteins orchestrate enzyme-ssDNA assembly during T4 recombination-dependent DNA replication and repair.

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

Helicase assembly protein Gp59 of bacteriophage T4: fluorescence anisotropy and sedimentation studies of complexes formed with derivatives of Gp32, the phage ssDNA binding protein.

Biochemistry·2001
Same author

Mutations in the N-terminal cooperativity domain of gene 32 protein alter properties of the T4 DNA replication and recombination systems.

The Journal of biological chemistry·2000
Same author

Relationship between hexamerization and ssDNA binding affinity in the uvsY recombination protein of bacteriophage T4.

Biochemistry·1999
Same author

Simultaneous interactions of bacteriophage T4 DNA replication proteins gp59 and gp32 with single-stranded (ss) DNA. Co-modulation of ssDNA binding activities in a DNA helicase assembly intermediate.

The Journal of biological chemistry·1999
Same author

In vitro selection of sequence contexts which enhance bypass of abasic sites and tetrahydrofuran by T4 DNA polymerase holoenzyme.

Journal of molecular biology·1999

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • DNA replication and recombination enzymes require access to single-stranded DNA (ssDNA).
  • Single-stranded DNA-binding proteins (SSBs) impede enzyme access to ssDNA, hindering complex formation.
  • A functional barrier exists for enzyme-ssDNA interactions due to SSB presence.

Purpose of the Study:

  • To identify and characterize proteins that facilitate enzyme access to ssDNA.
  • To investigate the mechanism by which these proteins overcome SSB inhibition.
  • To understand the conserved and species-specific roles of these mediator proteins in DNA metabolism.

Main Methods:

  • Biochemical assays to measure enzyme-ssDNA complex formation in the presence and absence of SSBs and mediator proteins.

Related Experiment Videos

  • Protein interaction studies to analyze the binding of mediator proteins to SSBs and DNA replication/recombination enzymes.
  • Comparative analysis of mediator protein function across different species.
  • Main Results:

    • A class of proteins, termed recombination/replication mediator proteins (RMPs), was identified.
    • RMPs were shown to promote the assembly of enzyme-ssDNA complexes by counteracting SSB inhibition.
    • RMPs exhibit conserved functions but possess species-specific interaction profiles with SSBs and enzymes.

    Conclusions:

    • RMPs are essential for efficient DNA replication and recombination by resolving SSB-mediated barriers.
    • The conserved function of RMPs highlights their fundamental importance in DNA processing across diverse organisms.
    • Species-specific interactions of RMPs with SSBs and enzymes allow for fine-tuning of DNA metabolic pathways.