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

Evidence for extrinsic exonucleolytic proofreading.

Stephanie A Nick McElhinny1, Youri I Pavlov, Thomas A Kunkel

  • 1Laboratory of Structural Biology, National Institute of Environmental Health Sciences, NIH, DHHS, Research Triangle Park, North Carolina 27709, USA.

Cell Cycle (Georgetown, Tex.)
|May 12, 2006
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

Persistence of large mtDNA rearrangements linked to premature aging in Pol γ exonuclease-deficient mice.

Nucleic acids research·2026
Same author

Evidence that MutSβ repairs indels generated by mispair initiated template slippage.

DNA repair·2026
Same author

Nonhomologous end-joining uses distinct mechanisms to repair each strand of a double strand break.

Nature communications·2025
Same author

Evidence that transient replication errors initiate nuclear genome mutations.

Nucleic acids research·2025
Same author

End Processing in NHEJ by Polymerase λ and PNKP is coordinated during short-range synapsis.

bioRxiv : the preprint server for biology·2025
Same author

Vulnerable Nucleotide Pools and Genomic Instability in Yeast Strains with Deletion of the <i>ADE12</i> Gene Encoding for Adenylosuccinate Synthetase.

International journal of molecular sciences·2025
Same journal

ALDH18A1 fuels spermine biosynthesis to sustain ferroptosis resistance in cancer and ischemia-reperfusion injury.

Cell cycle (Georgetown, Tex.)·2026
Same journal

Circular RNA circ_0001829 attenuates G2/M arrest to promote hepatocyte proliferation by sponging miR-3095-3p following liver injury.

Cell cycle (Georgetown, Tex.)·2026
Same journal

Identification of PGF+ endothelial cells associated with plaque instability in carotid atherosclerosis by scRNA-seq and RNA-seq analysis.

Cell cycle (Georgetown, Tex.)·2026
Same journal

BMSCs-derived exosomal miR-196a-5p promotes macrophage M2 polarization and osteogenesis in postmenopausal osteoporosis through regulating Rspo2/Wnt/β-catenin signaling.

Cell cycle (Georgetown, Tex.)·2026
Same journal

MicroRNA-6833-3p drives prostate cancer progression and stemness by targeting the NUMB-mediated NOTCH signaling pathway.

Cell cycle (Georgetown, Tex.)·2026
Same journal

OTUD5 promotes AML progression by stabilizing SLC7A11 to suppress ferroptosis.

Cell cycle (Georgetown, Tex.)·2026
See all related articles

DNA proofreading ensures genome stability. Some DNA polymerases lack proofreading, but extrinsic 3' exonucleases may edit their errors, differing from intrinsic proofreading mechanisms.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Exonucleolytic proofreading of DNA synthesis errors is crucial for maintaining genome stability.
  • Many DNA transactions involve polymerases lacking intrinsic 3' exonuclease activity, some exhibiting high inaccuracy.

Purpose of the Study:

  • To discuss evidence for extrinsic 3' exonuclease-mediated editing of DNA synthesis errors.
  • To compare extrinsic proofreading mechanisms with those intrinsic to replicative DNA polymerases.

Main Methods:

  • Literature review and synthesis of existing evidence.
  • Comparative analysis of DNA polymerase activities and proofreading mechanisms.

Main Results:

  • Evidence suggests that polymerases lacking intrinsic proofreading can be edited by separate 3' exonucleases.

Related Experiment Videos

  • Extrinsic proofreading mechanisms may differ significantly from intrinsic proofreading by replicative DNA polymerases.
  • Conclusions:

    • Extrinsic proofreading represents a potential mechanism for enhancing genome stability when intrinsic proofreading is absent.
    • Understanding these differences is key to comprehending the full spectrum of genome maintenance strategies.