Cryo-EM reveals open and closed Asgard chromatin assemblies
Harsh M Ranawat1, Marc K Cajili2, Natalia Lopez-Barbosa3
1Molecular Systems Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany; Collaboration for joint PhD degree between EMBL and Heidelberg University, Faculty of Biosciences, 69120 Heidelberg, Germany.
Molecular Cell
|October 29, 2025
Summary
This study reveals the first structures of Asgard chromatin, showing conserved closed and novel open hypernucleosomes. These findings offer insights into chromatin evolution and potential regulatory roles of ions.
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Structural Biology
Background:
- Asgard archaea are the closest archaeal relatives to eukaryotes.
- Understanding Asgard chromatin organization is crucial for tracing eukaryotic chromatin evolution.
- Previous knowledge of Asgard chromatin structure was limited.
Purpose of the Study:
- To determine the high-resolution structures of Asgard chromatin assemblies.
- To elucidate the chromatin organization in Asgard archaea.
- To understand the evolutionary implications of Asgard chromatin structure.
Main Methods:
- High-resolution cryo-electron microscopy (cryo-EM).
- Structural analysis of Hodarchaeal histone HHoB assemblies.
Main Results:
- First structures of Asgard chromatin assemblies reveal compact 'closed' and extended 'open' hypernucleosomes.
- The 'closed' conformation is conserved in archaea; the 'open' conformation resembles eukaryotic H3-H4 octasomes.
- Magnesium ions (Mg²⁺) were shown to influence Asgard chromatin conformation, suggesting a regulatory role.
Conclusions:
- Provides the first structure-based model of Asgard chromatin organization.
- Highlights conserved and novel aspects of chromatin architecture across archaeal and eukaryotic lineages.
- Expands understanding of chromatin evolution and potential ion-mediated regulation in Asgard archaea.
Related Concept Videos
Cryo-electron Microscopy
4.1K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
4.1K
Chromatin Packaging
21.3K
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...
21.3K
Chromatin Packaging
18.8K
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...
18.8K
Chromatin Packaging
9.5K
9.5K
Chromatin Immunoprecipitation- ChIP
12.1K
Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
12.1K


