Related Experiment Video
Updated: Jun 7, 2026

06:39
Live Cell Imaging of Chromosome Segregation During Mitosis
Published on: March 14, 2018
Chromosome segregation: taking the passenger seat
Gerben Vader1, Susanne M A Lens
1Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.
Current Biology : CB
|October 26, 2010
Summary
The chromosomal passenger complex (CPC) regulates chromosome segregation during cell division. Recent studies reveal how the CPC is precisely targeted to the inner centromere, a key step for accurate segregation.
Area of Science:
- Cell Biology
- Genetics
- Molecular Biology
Background:
- The chromosomal passenger complex (CPC) is essential for accurate chromosome segregation in both mitosis and meiosis.
- Proper localization of the CPC to the inner centromere is critical for its function.
- The precise mechanisms governing CPC inner centromere targeting have remained incompletely understood.
Purpose of the Study:
- To elucidate the molecular mechanisms responsible for the specific localization of the chromosomal passenger complex (CPC) to the inner centromere.
- To understand how CPC targeting contributes to the regulation of chromosome segregation.
- To provide a comprehensive view of CPC localization dynamics during cell division.
Main Methods:
- Utilized advanced microscopy techniques to visualize CPC localization in real-time.
- Employed genetic and biochemical approaches to identify key CPC-interacting proteins.
- Investigated the role of specific protein domains and post-translational modifications in CPC targeting.
Main Results:
- Identified novel protein interactions that mediate CPC recruitment to the inner centromere.
- Demonstrated that specific structural features of the inner centromere are crucial for CPC binding.
- Showcased how CPC localization is dynamically regulated throughout mitosis and meiosis.
Conclusions:
- The findings clarify the molecular basis of CPC inner centromere targeting, a fundamental process in cell division.
- This work enhances our understanding of how the CPC ensures faithful chromosome segregation.
- These insights pave the way for investigating CPC dysfunction in diseases associated with aneuploidy.
Related Concept Videos
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...
Microtubules and motor proteins exert two types of forces on...
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...
Microtubules and motor proteins exert two types of forces on...
Anaphase A and B
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...
Anaphase A and B
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...
Chromosomal Theory of Inheritance
In 1866, Gregor Mendel published the results of his pea plant breeding experiments, providing evidence for predictable patterns in the inheritance of physical characteristics. The significance of his findings was not immediately recognized. In fact, the existence of genes was unknown at the time. Mendel referred to hereditary units as “factors.”
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...
At the onset of anaphase, separase, a proteolytic enzyme, is...
