Related Experiment Video
Updated: Jun 13, 2025

10:52
Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets
Published on: August 13, 2016
9.7K
Microtubule depolymerization at kinetochores restricts anaphase spindle elongation
Biorxiv : the Preprint Server for Biology
|September 11, 2024
Summary
Central spindle sliding, not kinetochore microtubule depolymerization, drives chromosome separation during anaphase. This study reveals a direct link between the central spindle and chromosomes, challenging previous models of cell division.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Anaphase chromosome segregation relies on spindle microtubule forces.
- Current models propose forces are mediated via spindle poles, with central spindle sliding pushing poles apart and kinetochore microtubule (kMT) depolymerization pulling chromosomes poleward.
Purpose of the Study:
- To investigate the direct linkage between the central spindle and chromosomes during anaphase.
- To re-evaluate the forces driving chromosome segregation and spindle elongation.
Main Methods:
- Analysis of chromosome movement in monopolar spindles.
- Experimental manipulation of central spindle sliding in bipolar spindles.
- Varying the rate of kinetochore microtubule depolymerization.
Main Results:
- Chromosomes in monopolar spindles moved away from the pole, supporting central spindle sliding forces.
- Suppression of central spindle sliding constrained kMT depolymerization, indicating a direct kinetochore-central spindle linkage.
- Increased kMT depolymerization slowed pole separation without affecting chromosome separation velocity.
Conclusions:
- Central spindle sliding is the primary driver of anaphase chromosome separation.
- Kinetochore microtubule depolymerization acts as a limiting factor for spindle elongation, not a primary driver of chromosome movement.
Related Concept Videos
Anaphase A and B
4.0K
Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
4.0K
Spindle Assembly
3.6K
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
3.6K
The Mitotic Spindle
6.5K
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...
6.5K
The Spindle Assembly Checkpoint
3.1K
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...
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...
3.1K
Forces Acting on Chromosomes
3.3K
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...
Microtubules and motor proteins exert two types of forces on...
3.3K
Separation of Sister Chromatids
3.6K
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...
3.6K

