Related Experiment Video
Updated: May 5, 2026

05:35
Immunofluorescence Analysis of Endogenous and Exogenous Centromere-kinetochore Proteins
Published on: March 3, 2016
15.1K
The CINs of the centromere
1*Program in Molecular and Computational Biology, University of Southern California, Los Angeles, CA 90089-2910, U.S.A.
Biochemical Society Transactions
|November 22, 2013
Summary
Replication stress causes genome instability, particularly at centromeres, leading to chromosome loss. Loss of heterochromatin worsens this damage, contributing to cancer development.
Area of Science:
- Genetics
- Molecular Biology
- Cancer Research
Background:
- Replication stress is a known driver of genome instability.
- Centromeres are critical chromosomal regions susceptible to damage.
- Heterochromatin loss exacerbates genomic instability.
Purpose of the Study:
- To investigate the impact of replication stress on centromeric integrity.
- To explore the role of heterochromatin in centromere stability during replication stress.
Main Methods:
- Analysis of DNA damage markers at centromeres under replication stress conditions.
- Assessment of chromosome loss and rearrangements.
- Evaluation of heterochromatin status in stressed cells.
Main Results:
- Replication stress significantly increases DNA damage and rearrangements at centromeres.
- Loss of heterochromatin potentiates centromeric fragility and chromosome loss.
- These genomic alterations are linked to malignant growth.
Conclusions:
- Centromeres are vulnerable sites during replication stress, especially when heterochromatin is compromised.
- Replication-stress-induced centromeric instability contributes to the genetic alterations driving cancer.
More Related Videos
Related Concept Videos
Histone Variants at the Centromere
4.0K
Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
4.0K
Centrioles and Centrosomes
6.9K
Most animal cells comprise a pair of centrioles together called a centrosome. The cell duplicates its centrosome and contains two centrosomes side-by-side, which begin to move apart during the prophase. As the centrosomes migrate to two different sides of the cell, microtubules start extending from each centrosome toward the other end. The mitotic spindle is composed of the centrosomes and their emerging microtubules.
Near the end of the prophase, also called late prophase or...
Near the end of the prophase, also called late prophase or...
6.9K
Centrosome Duplication
3.7K
The primary microtubule organizing center (MTOC) in animal cells is the centrosome. A centrosome has two cylindrical centrioles at its core. Each centriole consists of nine sets of three microtubules held together by proteins. The centrioles are positioned at right angles to each other and surrounded by a shapeless protein cloud called the pericentriolar matrix, or pericentriolar material (PCM).
To ensure that each daughter cell receives a centrosome after cell division, centrosome duplication...
To ensure that each daughter cell receives a centrosome after cell division, centrosome duplication...
3.7K
Centrosome Duplication
2.6K
2.6K
Attachment of Sister Chromatids
3.1K
As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules. Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall...
3.1K
Attachment of Sister Chromatids
1.6K
1.6K

