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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...
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...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
DNA Damage can Stall the Cell Cycle02:36

DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...

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Related Experiment Video

Updated: Jun 18, 2026

Manipulation and Analysis of Cell Cycle-Dependent Processes in Budding Yeast
08:13

Manipulation and Analysis of Cell Cycle-Dependent Processes in Budding Yeast

Published on: September 26, 2025

Separating the spindle, checkpoint, and timer functions of BubR1.

Zohra Rahmani1, Mary E Gagou, Christophe Lefebvre

  • 1Institut Jacques Monod, Centre National de la Recherche Scientifique Unité Mixte de Recherche 7592, Université Paris Diderot, 75013 Paris, France.

The Journal of Cell Biology
|December 3, 2009
PubMed
Summary

BubR1

Area of Science:

  • Cell Biology
  • Genetics
  • Molecular Biology

Background:

  • BubR1 is crucial for mitosis, influencing the spindle assembly checkpoint (SAC), mitotic timing, and spindle function.
  • The interdependence of these BubR1 functions remains unclear.

Purpose of the Study:

  • To investigate the distinct roles of BubR1's kinase activity and KEN box in mitosis.
  • To determine the separability of BubR1's SAC, timer, and spindle functions.

Main Methods:

  • Analysis of kinase-dead (KD) BubR1 and N-terminal KEN box-lacking BubR1 mutants in Drosophila melanogaster.
  • Phenotypic analysis of mitotic processes, including SAC, spindle morphology, and mitotic timing.

Main Results:

  • Kinase-dead BubR1 mutants exhibit a robust SAC but abnormal spindles, indicating kinase activity modulates microtubule dynamics but is dispensable for SAC.

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Evaluation of the Spindle Assembly Checkpoint Integrity in Mouse Oocytes
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Last Updated: Jun 18, 2026

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Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
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Evaluation of the Spindle Assembly Checkpoint Integrity in Mouse Oocytes
10:09

Evaluation of the Spindle Assembly Checkpoint Integrity in Mouse Oocytes

Published on: September 13, 2022

  • BubR1-KEN mutants have normal spindles but lack SAC; mitotic timing remains normal if Mad2 is present.
  • BubR1's SAC, timer, and spindle functions are substantially separable.
  • Conclusions:

    • BubR1's kinase and KEN box domains mediate distinct functions in mitosis.
    • Mitotic fidelity in Drosophila can be maintained without a functional SAC, highlighting the redundancy of checkpoint mechanisms.