{"title":"Chromatin domains in the cell: Phase separation and condensation","authors":"Shin Fujishiro , Masaki Sasai , Kazuhiro Maeshima","doi":"10.1016/j.sbi.2025.103006","DOIUrl":null,"url":null,"abstract":"<div><div>Negatively charged genomic DNA wraps around positively charged core histone octamers to form nucleosomes, which, along with proteins and RNAs, self-organize into chromatin within the nucleus. In eukaryotic cells, chromatin forms loops that collapse into chromatin domains and serve as functional units of the genome. Chromatin domains vary in physical properties based on gene activity and are assembled into A (euchromatin) and B (heterochromatin) compartments. Since various factors—such as chromatin-binding proteins, histone modifications, transcriptional states, depletion attraction, and cations—can significantly impact chromatin organization, the formation processes of these hierarchical structures remain unclear. No single imaging, genomics, or modeling method can provide a complete picture of the process. Beautiful models can sometimes fool our thinking. In this short review, we critically discuss the formation mechanisms of the chromatin domain in the cell from a physical point of view, including phase separation and condensation.</div></div>","PeriodicalId":10887,"journal":{"name":"Current opinion in structural biology","volume":"91 ","pages":"Article 103006"},"PeriodicalIF":6.1000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in structural biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0959440X25000247","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Negatively charged genomic DNA wraps around positively charged core histone octamers to form nucleosomes, which, along with proteins and RNAs, self-organize into chromatin within the nucleus. In eukaryotic cells, chromatin forms loops that collapse into chromatin domains and serve as functional units of the genome. Chromatin domains vary in physical properties based on gene activity and are assembled into A (euchromatin) and B (heterochromatin) compartments. Since various factors—such as chromatin-binding proteins, histone modifications, transcriptional states, depletion attraction, and cations—can significantly impact chromatin organization, the formation processes of these hierarchical structures remain unclear. No single imaging, genomics, or modeling method can provide a complete picture of the process. Beautiful models can sometimes fool our thinking. In this short review, we critically discuss the formation mechanisms of the chromatin domain in the cell from a physical point of view, including phase separation and condensation.
期刊介绍:
Current Opinion in Structural Biology (COSB) aims to stimulate scientifically grounded, interdisciplinary, multi-scale debate and exchange of ideas. It contains polished, concise and timely reviews and opinions, with particular emphasis on those articles published in the past two years. In addition to describing recent trends, the authors are encouraged to give their subjective opinion of the topics discussed.
In COSB, we help the reader by providing in a systematic manner:
1. The views of experts on current advances in their field in a clear and readable form.
2. Evaluations of the most interesting papers, annotated by experts, from the great wealth of original publications.
[...]
The subject of Structural Biology is divided into twelve themed sections, each of which is reviewed once a year. Each issue contains two sections, and the amount of space devoted to each section is related to its importance.
-Folding and Binding-
Nucleic acids and their protein complexes-
Macromolecular Machines-
Theory and Simulation-
Sequences and Topology-
New constructs and expression of proteins-
Membranes-
Engineering and Design-
Carbohydrate-protein interactions and glycosylation-
Biophysical and molecular biological methods-
Multi-protein assemblies in signalling-
Catalysis and Regulation