Related Experiment Video
Updated: Nov 10, 2025

07:14
Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
Published on: September 20, 2019
8.5K
Back to the new beginning: Mitotic exit in space and time
1College of Medicine, Health and Life Science, Centre for Genomic Engineering and Maintenance (CenGEM), Brunel University London, Uxbridge UB8 3PH, UK.
Seminars in Cell & Developmental Biology
|April 3, 2021
Summary
Cell division aims to create identical daughter cells. Mitotic exit, crucial for cell cycle completion and rebuilding, is a complex, regulated process involving protein phosphorylation and spatial control.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Cell division produces two identical daughter cells.
- Mitotic exit completes genome separation and rebuilds cellular structures for the next cell cycle.
- This stage of mitosis is less understood compared to early stages, with recent research highlighting its complexity.
Purpose of the Study:
- To review recent advances in understanding mitotic exit.
- To discuss the role of protein phosphorylation/de-phosphorylation and spatial regulation in mitotic exit.
- To highlight consensus, contrasting views, and unanswered questions in the field.
Main Methods:
- Literature review of recent advances in cell division research.
- Analysis of key molecular mechanisms regulating mitotic exit.
- Synthesis of current understanding regarding spatial and temporal regulation.
Main Results:
- Mitotic exit is not a simple reversal of mitotic entry but a highly regulated process.
- Protein phosphorylation and de-phosphorylation play key roles in mitotic exit.
- Spatial regulation is a critical, emerging concept in understanding mitotic exit.
Conclusions:
- Recent research has significantly advanced our understanding of mitotic exit.
- Further investigation is needed to resolve contrasting views and answer outstanding questions.
- Mitotic exit is a dynamic and precisely controlled transition in the cell cycle.
Related Concept Videos
Meiosis vs. Mitosis
63.7K
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...
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
63.7K
The Mitotic Spindle
7.1K
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...
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures...
7.1K
M-Cdk Drives Transition Into Mitosis
5.9K
Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
5.9K
Meiosis II
48.3K
Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
48.3K
Meiosis II
189.1K
Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each...
189.1K
Separation of Sister Chromatids
4.0K
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...
At the onset of anaphase, separase, a proteolytic enzyme, is...
4.0K

