Related Experiment Video
Updated: Jun 9, 2025

08:52
Chemical Dimerization-Induced Protein Condensates on Telomeres
Published on: April 12, 2021
3.1K
Dinochromosome Heterotermini with Telosomal Anchorages
Alvin Chun Man Kwok1, Kosmo Ting Hin Yan1, Shaoping Wen1
1Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.
International Journal of Molecular Sciences
|October 26, 2024
Summary
Dinoflagellate chromosomes possess unique telomeric nucleosomes anchoring them to the nuclear envelope. These telomeric nucleosomes are crucial for chromosomal stability and cell cycle progression.
Area of Science:
- Cell Biology
- Genetics
- Molecular Biology
Background:
- Dinoflagellate chromosomes (BfCs) have large genomes but lack typical nucleosomal protection.
- BfCs interact with extranuclear microtubules at the intact nuclear envelope (NE) throughout the cell cycle.
Purpose of the Study:
- Investigate the structure and function of dinoflagellate chromosome ends.
- Determine the role of histones and nucleosomes in BfC organization and NE anchorage.
Main Methods:
- Utilized ultrastructural studies, polarized light and fluorescence microscopy.
- Employed micrococcal nuclease-resistant profiles (MNRPs) and 2D gel electrophoresis.
- Conducted histone H3K9me3 inhibition and sirtinol treatment experiments.
Main Results:
- NE-associated chromosome ends were observed to persist post-mitosis.
- Histone H3K9me3 inhibition caused S-G2 cell cycle delay.
- Telomeric nucleosomes (TNs) were identified as the primary histone structures, enriched at the NE.
Conclusions:
- Telomeric repeats form the major octameric MNRPs responsible for chromosomal anchorage at the NE.
- Telomeric nucleosomes play a key role in dinoflagellate chromosome organization and nuclear envelope interaction.
Related Concept Videos
Telomeres and Telomerase
23.1K
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded...
23.1K
Histone Variants at the Centromere
4.3K
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...
4.3K
Polytene Chromosomes
10.0K
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...
10.0K
Attachment of Sister Chromatids
3.2K
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...
3.2K
Chromosome Structure
22.6K
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...
22.6K
Lampbrush Chromosomes
7.9K
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...
7.9K

