Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Chromatin Packaging02:21

Chromatin Packaging

16.9K
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...
16.9K
Chromatin Packaging01:32

Chromatin Packaging

16.3K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
16.3K
Chromatin Packaging02:21

Chromatin Packaging

9.0K
9.0K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

6.1K
The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
6.1K
Euchromatin01:01

Euchromatin

6.7K
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...
6.7K
Heterochromatin02:38

Heterochromatin

12.0K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
12.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Independent Prognostic Contributions of Anti-Ro52 and Anti-MDA5 in Autoimmune-Associated Interstitial Lung Disease.

ChestĀ·2026
Same author

Evolutionary Origin of Prolonged Delayed Fertilization in the Fagaceae.

Ecology and evolutionĀ·2026
Same author

Linker histone H1 functions as a liquid-like glue to organize chromatin in living human cells.

Science advancesĀ·2026
Same author

FPGA-accelerated streaming data reduction achieving an average compression ratio over 8000 in a 17.4 kHz, 840 kpixel CITIUS detector for quasi-elastic gamma-ray scattering.

Journal of synchrotron radiationĀ·2026
Same author

Cohesin prevents local mixing of condensed euchromatic domains in living human cells.

bioRxiv : the preprint server for biologyĀ·2026
Same author

Comparison of oxygenation targets in critically ill adults: a systematic review and network meta-analysis of randomized controlled trials.

American journal of respiratory and critical care medicineĀ·2026

Related Experiment Video

Updated: Apr 25, 2026

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
09:32

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

Published on: October 14, 2022

6.4K

Chromatin structure revealed by X-ray scattering analysis and computational modeling.

Kazuhiro Maeshima1, Ryosuke Imai2, Takaaki Hikima3

  • 1Biological Macromolecules Laboratory, Structural Biology Center, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan; Department of Genetics, School of Life Science, Graduate University for Advanced Studies (Sokendai), Mishima, Shizuoka 411-8540, Japan; RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148, Japan.

Methods (San Diego, Calif.)
|August 30, 2014
PubMed
Summary

Human DNA organization remains unclear. Small-angle X-ray scattering (SAXS) reveals chromatin primarily consists of irregularly folded nucleosome fibers, challenging the existence of the 30-nm chromatin structure.

Keywords:
30-nm chromatin fiberChromatinChromosomesComputational modelingCryo-electron microscopySmall-angle X-ray scattering

More Related Videos

Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique
06:32

Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique

Published on: March 9, 2022

1.8K
Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA
10:40

Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA

Published on: September 10, 2013

22.1K

Related Experiment Videos

Last Updated: Apr 25, 2026

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
09:32

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

Published on: October 14, 2022

6.4K
Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique
06:32

Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique

Published on: March 9, 2022

1.8K
Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA
10:40

Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA

Published on: September 10, 2013

22.1K

Area of Science:

  • Molecular Biology
  • Genetics
  • Biophysics

Background:

  • The organization of 2 meters of human genomic DNA within each cell is not fully understood.
  • Classical models propose DNA is packaged into an 11-nm nucleosome fiber, then further folded into a 30-nm chromatin fiber, potentially forming larger helical structures.

Purpose of the Study:

  • To investigate the bulk structure of interphase chromatin and mitotic chromosomes.
  • To determine if the proposed 30-nm chromatin fiber structure exists in vivo.

Main Methods:

  • Small-angle X-ray scattering (SAXS) was employed to analyze the structural features of chromatin.
  • Computational analysis of "in silico condensed chromatin" was used to interpret SAXS data.

Main Results:

  • SAXS analysis detected no structural features larger than the 11-nm nucleosome fiber.
  • The results suggest that chromatin in interphase nuclei and mitotic chromosomes is composed of irregularly folded nucleosome fibers.
  • The classical 30-nm chromatin fiber structure was not detected.

Conclusions:

  • The textbook model of chromatin organization, including the 30-nm fiber, may not accurately represent the in vivo structure.
  • Chromatin appears to exist primarily as irregularly folded 11-nm nucleosome fibers.
  • Further discussion on alternative methods for chromatin structure investigation is provided.