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

A cell-counting factor regulating structure size in Dictyostelium.

D A Brock1, R H Gomer

  • 1Howard Hughes Medical Institute, Department of Biochemistry and Cell Biology MS-140, Rice University, Houston, Texas 77005-1892, USA.

Genes & Development
|August 13, 1999
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

Concurrent coevolution of intra-organismal cheaters and resisters.

Journal of evolutionary biology·2015
Same author

Complexity of the Neurospora crassa circadian clock system: multiple loops and oscillators.

Cold Spring Harbor symposia on quantitative biology·2008
Same author

Overexpression of White Collar-1 (WC-1) activates circadian clock-associated genes, but is not sufficient to induce most light-regulated gene expression in Neurospora crassa.

Molecular microbiology·2002
Same author

ABC transporters required for endocytosis and endosomal pH regulation in Dictyostelium.

Journal of cell science·2001
Same author

Not being the wrong size.

Nature reviews. Molecular cell biology·2001
Same author

A cell number-counting factor regulates group size in Dictyostelium by differentially modulating cAMP-induced cAMP and cGMP pulse sizes.

The Journal of biological chemistry·2001

Dictyostelium cells use a secreted "counting factor" to regulate fruiting body size. Disrupting the counting gene leads to massive fruiting bodies, revealing its role in cell aggregation control.

Area of Science:

  • Cellular and Molecular Biology
  • Developmental Biology
  • Biochemistry

Background:

  • Dictyostelium discoideum cells aggregate to form multicellular structures and fruiting bodies.
  • The size of these fruiting bodies is regulated by complex signaling pathways.
  • Previous observations indicated that specific mutations affect the final size of the fruiting bodies.

Purpose of the Study:

  • To identify and characterize the factor responsible for regulating the size of Dictyostelium cell aggregates.
  • To understand the molecular mechanism by which this factor controls cell grouping and fruiting body formation.
  • To investigate the role of the 'counting' gene in this process.

Main Methods:

  • Purification of the unknown factor secreted by smlA cells.

Related Experiment Videos

  • Biochemical characterization of the purified factor, including molecular mass determination.
  • Genetic analysis using gene disruption of the identified 'counting' gene.
  • Microscopic observation of cell aggregation and fruiting body development in wild-type and mutant strains.
  • Main Results:

    • A 450 kD polypeptide complex, termed the "counting factor," was purified.
    • A 40 kD hydrophilic protein, named "counting," was identified as a component of this complex.
    • Disruption of the "counting" gene abolished the secretion of the counting factor.
    • Mutant cells formed significantly larger fruiting bodies due to the lack of aggregation stream breakup.

    Conclusions:

    • The "counting" gene product is essential for the secretion of the counting factor.
    • The counting factor plays a critical role in regulating the size of Dictyostelium cell aggregates and subsequent fruiting bodies.
    • This mechanism provides insight into how cell populations coordinate to form structures of specific sizes.