Related Experiment Video
Updated: Jan 22, 2026

07:14
Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
Published on: September 20, 2019
8.7K
High-resolution imaging reveals how the spindle midzone impacts chromosome movement
Melissa C Pamula1, Lina Carlini1, Scott Forth2
1Laboratory of Chemistry and Cell Biology, The Rockefeller University, New York, NY.
The Journal of Cell Biology
|June 29, 2019
Summary
Microtubule bundles in dividing cells restrict chromosome movement by reducing overlap length. This process is crucial for proper chromosome segregation and positioning within daughter cells.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Microtubule bundles in the spindle midzone play a role in chromosome segregation during cell division.
- The precise mechanisms by which these bundles influence chromosome movement are not fully understood.
Purpose of the Study:
- To investigate the role of microtubule bundles and the protein PRC1 in chromosome segregation during anaphase.
- To elucidate how microtubule bundle dynamics affect chromosome movement and spindle elongation.
Main Methods:
- High-resolution live-cell imaging of dividing human cells.
- Analysis of microtubule bundles, growing filaments, and chromosome dynamics.
- Depletion of PRC1 via knockdown and expression of a mutant PRC1.
Main Results:
- Microtubule bundle filament overlap length decreases during anaphase, correlating with slowed chromosome segregation.
- Preventing microtubule bundle assembly via PRC1 knockdown increases chromosome segregation distance and rate.
- Mutant PRC1 with reduced microtubule affinity still allows bundle assembly but leads to chromosome hypersegregation.
Conclusions:
- Reduced microtubule overlap length within bundles is essential for restricting spindle elongation.
- This restriction is necessary for proper chromosome positioning in daughter cells.
- The protein PRC1 plays a critical role in regulating microtubule bundle dynamics and ensuring accurate chromosome segregation.
Related Concept Videos
Chromosome Structure
26.0K
A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
26.0K
Polytene Chromosomes
10.9K
Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also...
10.9K
Lampbrush Chromosomes
8.6K
In 1882, Flemming observed lampbrush chromosomes (LBC) in salamander eggs. Later in 1892, Rückert observed LBCs in shark egg cells and coined the term "lampbrush chromosomes" because they looked like brushes used to clean kerosene lamps.
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops...
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops...
8.6K
Chromosome Replication
10.5K
Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins. This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin...
10.5K
The Mitotic Spindle
7.8K
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...
7.8K
Spindle Assembly
4.2K
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...
4.2K

