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 Concept Videos

Forces Acting on Chromosomes02:11

Forces Acting on Chromosomes

During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis. 
Microtubules and motor proteins exert two types of forces on...
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
The Mitotic Spindle02:27

The Mitotic Spindle

The mitotic spindle—or spindle apparatus—is a eukaryotic, cytoskeletal structure made up of long protein fibers called microtubules. Formed during cell division, the spindle separates sister chromatids and moves them to opposite ends of a parental cell, where the now individual chromosomes are distributed to two daughter cell nuclei.
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The Mitotic Spindle02:27

The Mitotic Spindle

The mitotic spindle—or spindle apparatus—is a eukaryotic, cytoskeletal structure made up of long protein fibers called microtubules. Formed during cell division, the spindle separates sister chromatids and moves them to opposite ends of a parental cell, where the now individual chromosomes are distributed to two daughter cell nuclei.
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The Spindle Assembly Checkpoint02:19

The Spindle Assembly Checkpoint

The spindle assembly checkpoint is a molecular surveillance mechanism ensuring the fidelity of chromosome segregation during anaphase. The checkpoint monitors the completion of all the prerequisite steps before chromosome segregation to determine whether the segregation process should proceed or be delayed.
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
Nondisjunction01:29

Nondisjunction

During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Bora, CEP192 and Cenexin regulate distinct Plk1-dependent cell and centrosome cycle transitions.

Nature communications·2026
Same author

Tipping the balance: synthesis and evaluation of centrinone-based degraders of polo-like kinase 4.

RSC chemical biology·2026
Same author

SDS-22 stabilizes GSP-1/-2 PP1 subunits contributing to polarity establishment in C. elegans embryos.

EMBO reports·2025
Same author

SDS-22 stabilizes the PP1 catalytic subunits GSP-1/-2 contributing to polarity establishment in <i>C. elegans</i> embryos.

bioRxiv : the preprint server for biology·2025
Same author

Spatio-temporal control of mitosis using light via a Plk1 inhibitor caged for activity and cellular permeability.

Nature communications·2025
Same author

Internal feedback circuits among MEX-5, MEX-6, and PLK-1 maintain faithful patterning in the <i>Caenorhabditis elegans</i> embryo.

Proceedings of the National Academy of Sciences of the United States of America·2024

Related Experiment Video

Updated: May 15, 2026

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
07:14

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

Mitotic spindle (DIS)orientation and DISease: cause or consequence?

Anna Noatynska1, Monica Gotta, Patrick Meraldi

  • 1Department of Physiology and Metabolism, University of Geneva, 1211 Geneva, Switzerland.

The Journal of Cell Biology
|December 26, 2012
PubMed
Summary

Spindle orientation defects can cause cell division errors linked to cancer and brain diseases. This review explores if these defects directly cause disease or are merely associated side effects.

More Related Videos

Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets
10:52

Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets

Published on: August 13, 2016

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel
08:29

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel

Published on: May 14, 2018

Related Experiment Videos

Last Updated: May 15, 2026

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
07:14

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets
10:52

Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets

Published on: August 13, 2016

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel
08:29

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel

Published on: May 14, 2018

Area of Science:

  • Cell Biology
  • Developmental Biology
  • Genetics

Background:

  • Correct mitotic spindle alignment is essential for cell fate, tissue organization, and development.
  • Spindle orientation defects are implicated in human brain diseases and cancer.
  • These defects may disrupt the balance of symmetric and asymmetric cell divisions, affecting proliferation.

Purpose of the Study:

  • To investigate the causal role of spindle orientation defects in diseases linked to mutations in multi-functional genes.
  • To differentiate between direct causation and correlative side effects of spindle defects in disease pathogenesis.

Main Methods:

  • Literature review and analysis of genetic studies linking spindle orientation to disease.
  • Examination of protein functions for genes associated with spindle defects and disease phenotypes.

Main Results:

  • Many genes linked to spindle defects have multiple cellular roles, complicating direct causal links.
  • The precise contribution of spindle orientation defects versus other protein functions to disease remains unclear.

Conclusions:

  • Spindle orientation defects are strongly associated with various diseases, but their direct causal role requires further investigation.
  • Distinguishing direct causation from correlative effects is critical for understanding disease mechanisms and developing targeted therapies.