Related Experiment Video
Updated: Jul 19, 2025

09:52
Probing The Structure And Dynamics Of Nucleosomes Using Atomic Force Microscopy Imaging
Published on: January 31, 2019
11.7K
Structure and Dynamics of Compact Dinucleosomes: Analysis by Electron Microscopy and spFRET
Maria E Stefanova1, Olesya I Volokh1, Oleg V Chertkov1
1Biology Faculty, Lomonosov Moscow State University, Moscow 119234, Russia.
International Journal of Molecular Sciences
|August 12, 2023
Summary
Compact dinucleosomes (CODIs) are dynamic structures where nucleosomal DNA can uncoil from histone octamers. This destabilization, influenced by spacing, suggests CODIs may be intermediates in chromatin disruption.
Area of Science:
- Molecular biology
- Chromatin dynamics
- Epigenetics
Background:
- Compact dinucleosomes (CODIs) form at active regulatory DNA regions.
- The structural heterogeneity and dynamics of CODIs remain poorly understood.
Purpose of the Study:
- To investigate the structure and dynamics of CODIs.
- To determine the role of internucleosomal spacing in chromatin stability.
Main Methods:
- Single-particle Förster resonance energy transfer (spFRET) microscopy in solution and gel.
- Electron microscopy analysis.
Main Results:
- A fraction of CODIs exhibit significant uncoiling of nucleosomal DNA from the histone octamer.
- Electron microscopy suggests up to 30 bp of DNA transiently uncoil/recoil on the histone octamer.
- The histone chaperone Spt6 does not stabilize the more open nucleosome structure in CODIs.
Conclusions:
- CODIs display structural heterogeneity and dynamics, with some nucleosomes being destabilized.
- Proper internucleosomal spacing is crucial for maintaining chromatin stability.
- CODIs may serve as intermediates in chromatin disruption processes.
Related Concept Videos
The Nucleosome Core Particle
12.2K
Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
12.2K
The Nucleosome
1.7K
Human DNA is almost two meters long. However, it is compressed inside a tiny nucleus measuring only a few microns in diameter. To make this degree of compaction possible, DNA is organized into several sequential levels so that it can fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
In a chromosome, DNA is wound twice around a protein complex called a histone octamer core, which consists of 8 histone proteins. This...
In a chromosome, DNA is wound twice around a protein complex called a histone octamer core, which consists of 8 histone proteins. This...
1.7K
Chromatin Packaging
15.5K
Each human somatic cell contains 6 billion base-pairs of DNA. Each base-pair is 0.34 nm long, which means that each diploid cell contains a staggering 2 meters of DNA. How is such a long DNA strand packed inside a nucleus measuring only 10 - 20 microns in diameter?
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
15.5K
Studying the Cytoskeleton
6.3K
The cytoskeletal architecture can be studied using different microscopic and biochemical techniques. Electron microscopy was instrumental in discovering the cytoskeletal architecture around the 1960s, which allowed obtaining structural information at a high-resolution level. However, the sample preparation procedure often limits this ability in biological samples. Several protocols have been developed over the years to optimize sample preparation. In one of the protocols known as rotary...
6.3K
Euchromatin
7.0K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions take up more dye, appearing darker, while the less-compact areas take up less dye and appear lighter. Based on the compaction level, chromatins are classified into two primary forms – euchromatin and heterochromatin.
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
7.0K
Nucleosome Remodeling
9.2K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
9.2K

