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Updated: Jun 26, 2026

Live Cell Imaging of Chromosome Segregation During Mitosis
Published on: March 14, 2018
TMAP/CKAP2 is essential for proper chromosome segregation
Kyung Uk Hong1, Eunhee Kim, Chang-Dae Bae
1Department of Molecular Cell Biology and Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Jangangu, Suwon Republic of Korea.
Abstract:
Tumor-associated microtubule-associated protein (TMAP), also known as cytoskeleton associated protein 2 (CKAP2), is a novel mitotic spindle-associated protein which is frequently up-regulated in various malignances. However, its cellular functions remain unknown. Previous reports suggested that the cellular functions of TMAP/CKAP2 pertain to regulation of the dynamics and assembly of the mitotic spindle. To investigate its role in mitosis, we studied the effects of siRNA-mediated depletion of TMAP/CKAP2 in cultured mammalian cells. Unexpectedly, TMAP/CKAP2 knockdown did not result in significant alterations of the spindle apparatus. However, TMAP/CKAP2-depleted cells often exhibited abnormal nuclear morphologies, which were accompanied by abnormal organization of the nuclear lamina, and chromatin bridge formation between two daughter cell nuclei. Time lapse video microscopy revealed that the changes in nuclear morphology and chromatin bridge formations observed in TMAP/CKAP2-depleted cells are the result of defects in chromosome segregation. Consistent with this, the spindle checkpoint activity was significantly reduced in TMAP/CKAP2-depleted cells. Moreover, chromosome missegregation induced by depletion of TMAP/CKAP2 ultimately resulted in reduced cell viability and increased chromosomal instability. Our present findings demonstrate that TMAP/CKAP2 is essential for proper chromosome segregation and for maintaining genomic stability.
Insights
Tumor-associated microtubule-associated protein (TMAP/CKAP2) is crucial for accurate chromosome segregation during cell division. Its depletion leads to genomic instability and reduced cell viability, highlighting its role beyond spindle regulation.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Tumor-associated microtubule-associated protein (TMAP), also known as cytoskeleton associated protein 2 (CKAP2), is upregulated in malignancies.
- The precise cellular functions of TMAP/CKAP2, particularly in mitosis, are not fully understood.
- Previous research suggested TMAP/CKAP2 involvement in mitotic spindle dynamics and assembly.
Purpose of the Study:
- To investigate the role of TMAP/CKAP2 in mitosis and chromosome segregation.
- To determine the cellular consequences of TMAP/CKAP2 depletion in mammalian cells.
Main Methods:
- siRNA-mediated depletion of TMAP/CKAP2 in cultured mammalian cells.
- Analysis of spindle apparatus, nuclear morphology, and nuclear lamina organization.
- Time-lapse video microscopy to observe cellular dynamics.
- Assessment of spindle checkpoint activity, cell viability, and chromosomal instability.
Main Results:
- TMAP/CKAP2 knockdown did not significantly alter the mitotic spindle apparatus.
- Depletion resulted in abnormal nuclear morphologies, nuclear lamina disorganization, and chromatin bridges.
- Defects in chromosome segregation and reduced spindle checkpoint activity were observed.
- Chromosome missegregation led to decreased cell viability and increased chromosomal instability.
Conclusions:
- TMAP/CKAP2 is essential for proper chromosome segregation during mitosis.
- TMAP/CKAP2 plays a critical role in maintaining genomic stability.
- The function of TMAP/CKAP2 extends beyond spindle regulation to encompass nuclear integrity and accurate cell division.
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