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

ACE2, CBK1, and BUD4 in budding and cell separation.

Warren P Voth1, Aileen E Olsen, Mohammed Sbia

  • 1Department of Pathology, University of Utah, 30 North 1900 East, Salt Lake City, UT 84132-2501, USA.

Eukaryotic Cell
|June 11, 2005
PubMed
Summary

The RAM network and Ace2 transcription factor regulate cell growth and division in yeast. This study reveals Ace2 acts downstream of the RAM network, impacting cell separation and morphology.

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

MicroRNA-146a Protects against Hepatocellular Carcinoma through Suppression of CCL5.

Cancer research communications·2026
Same author

MicroRNA-146a protects against hepatocellular carcinoma through suppression of CCL5.

Cancer research communications·2026
Same author

microRNA-21 promotes dysregulated lipid metabolism and hepatocellular carcinoma.

bioRxiv : the preprint server for biology·2025
Same author

Erratum: HAF prevents hepatocyte apoptosis and progression to MASH and HCC through transcriptional regulation of the NF-κB pathway.

Hepatology (Baltimore, Md.)·2025
Same author

A microRNA-regulated transcriptional state defines intratumoral CD8<sup>+</sup> T cells that respond to immunotherapy.

Cell reports·2025
Same author

HAF prevents hepatocyte apoptosis and progression to MASH and HCC through transcriptional regulation of the NF-κB pathway.

Hepatology (Baltimore, Md.)·2024

Area of Science:

  • Cell Biology
  • Molecular Genetics
  • Yeast Biology

Background:

  • Mutations in RAM network genes (CBK1, MOB2, KIC1, HYM1, TAO3) disrupt yeast cell polarity and morphology.
  • These defects overlap with phenotypes observed in Ace2 transcription factor mutants, including altered colony morphology and cell separation issues.
  • Ace2 and its paralog Swi5 are key regulators of gene expression involved in cell cycle and morphogenesis.

Purpose of the Study:

  • To elucidate the relationship between the RAM network and the Ace2 transcription factor.
  • To investigate the roles of Ace2, Cbk1, and Bud4 in yeast bud site selection, polarized growth, and cell separation.
  • To characterize the genetic interactions and regulatory pathways governing these cellular processes.

Main Methods:

  • Genetic analysis of RAM network and Ace2/Swi5 mutants in yeast (Saccharomyces cerevisiae).

Related Experiment Videos

  • Plasmid-based complementation assays to assess gene function and pathway relationships.
  • Timed sedimentation assays to quantify cytokinesis defects and analyze cell shape.
  • Analysis of gene expression for Ace2 and Swi5 target genes.
  • Main Results:

    • Ace2 functions downstream of the RAM network, with reduced Ace2 activity contributing to RAM mutant phenotypes.
    • A novel timed sedimentation assay effectively quantifies cytokinesis defects and budding patterns.
    • Ace2 and Cbk1 possess both shared transcriptional roles (e.g., CTS1 regulation) and independent functions in cell polarization and separation.
    • Genetic interactions between bud4, ace2, and cbk1 mutants reveal complex regulatory networks.

    Conclusions:

    • The RAM network and Ace2 pathway are crucial for proper yeast cell division and polarity.
    • Ace2 is a key downstream effector of the RAM network, mediating phenotypes related to cell separation and morphology.
    • Distinct and overlapping functions of Ace2, Cbk1, and Bud4 highlight the intricate regulation of yeast morphogenesis.