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

APC activators caught by their tails?

Hartmut C Vodermaier1, Jan-Michael Peters

  • 1Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, Vienna, Austria. vodermaier@imp.univie.ac.at

Cell Cycle (Georgetown, Tex.)
|January 17, 2004
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

A modular framework for automated segmentation and analysis of AFM imaging of chromatin organization.

Nucleic acids research·2026
Same author

PDS5 proteins control genome architecture by limiting the lifetime of cohesin-NIPBL complexes.

Molecular cell·2026
Same author

Chromatin boundary permeability is controlled by CTCF conformational ensembles.

bioRxiv : the preprint server for biology·2025
Same author

Two CTCF motifs impede cohesin-mediated DNA loop extrusion.

Molecular cell·2025
Same author

The mitotic STAG3-cohesin complex shapes male germline nucleome.

Nature structural & molecular biology·2025
Same author

NIPBL and STAG1 enable loop extrusion by providing differential DNA-cohesin affinity.

Proceedings of the National Academy of Sciences of the United States of America·2025
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
Same journal

MITF-Driven melanoma plasticity as a core mechanism of therapy resistance: integrating microenvironmental signaling, mechanotransduction, and metabolic reprogramming.

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

The Anaphase-Promoting Complex (APC), a key regulator of cell division, remains complex. Recent studies reveal its architecture and activator recruitment, advancing our understanding of APC activation.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • The Anaphase-Promoting Complex (APC) is a crucial ubiquitin ligase essential for regulating mitotic progression.
  • Despite its importance, the structural complexity and activation mechanisms of the APC have remained largely enigmatic.
  • Understanding APC function is vital for comprehending cell cycle control and preventing developmental abnormalities.

Purpose of the Study:

  • To elucidate the structural architecture of the Anaphase-Promoting Complex (APC).
  • To investigate the mechanisms governing the recruitment of activators to the APC.
  • To integrate recent findings into a cohesive understanding of APC activation processes.

Main Methods:

  • Utilized biochemical approaches to dissect the APC's structural components.

Related Experiment Videos

  • Employed genetic studies to identify and characterize APC activators and their interactions.
  • Synthesized data from recent publications to provide a comprehensive overview.
  • Main Results:

    • Recent research has shed light on the intricate architecture of the APC.
    • Key insights have been gained into how specific activators are recruited to the APC complex.
    • These findings provide a clearer picture of the dynamic regulation of APC activity.

    Conclusions:

    • The APC's complexity is being unraveled through integrated biochemical and genetic studies.
    • Understanding APC activator recruitment is critical for comprehending its role in mitotic control.
    • These advancements significantly enhance our knowledge of APC activation and its implications for cell cycle regulation.