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Nucleosome Clutches are Regulated by Chromatin Internal Parameters.
- Source :
-
Journal of molecular biology [J Mol Biol] 2021 Mar 19; Vol. 433 (6), pp. 166701. Date of Electronic Publication: 2020 Nov 09. - Publication Year :
- 2021
-
Abstract
- Nucleosomes cluster together when chromatin folds in the cell to form heterogeneous groups termed "clutches". These structural units add another level of chromatin regulation, for example during cell differentiation. Yet, the mechanisms that regulate their size and compaction remain obscure. Here, using our chromatin mesoscale model, we dissect clutch patterns in fibers with different combinations of nucleosome positions, linker histone density, and acetylation levels to investigate their role in clutch regulation. First, we isolate the effect of each chromatin parameter by studying systems with regular nucleosome spacing; second, we design systems with naturally-occurring linker lengths that fold onto specific clutch patterns; third, we model gene-encoding fibers to understand how these combined factors contribute to gene structure. Our results show how these chromatin parameters act together to produce different-sized nucleosome clutches. The length of nucleosome free regions (NFRs) profoundly affects clutch size, while the length of linker DNA has a moderate effect. In general, higher linker histone densities produce larger clutches by a chromatin compaction mechanism, while higher acetylation levels produce smaller clutches by a chromatin unfolding mechanism. We also show that it is possible to design fibers with naturally-occurring DNA linkers and NFRs that fold onto specific clutch patterns. Finally, in gene-encoding systems, a complex combination of variables dictates a gene-specific clutch pattern. Together, these results shed light into the mechanisms that regulate nucleosome clutches and suggest a new epigenetic mechanism by which chromatin parameters regulate transcriptional activity via the three-dimensional folded state of the genome at a nucleosome level.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2020 Elsevier Ltd. All rights reserved.)
- Subjects :
- Acetylation
Animals
Chromatin Assembly and Disassembly
DNA chemistry
DNA genetics
DNA metabolism
Genetic Loci
Histones genetics
Histones metabolism
Homeodomain Proteins genetics
Homeodomain Proteins metabolism
Humans
Mice
Molecular Dynamics Simulation
Nucleic Acid Conformation
Nucleosomes genetics
Nucleosomes metabolism
Octamer Transcription Factor-3 genetics
Octamer Transcription Factor-3 metabolism
Protein Conformation
Epigenesis, Genetic
Genome
Histones chemistry
Homeodomain Proteins chemistry
Nucleosomes ultrastructure
Octamer Transcription Factor-3 chemistry
Protein Processing, Post-Translational
Subjects
Details
- Language :
- English
- ISSN :
- 1089-8638
- Volume :
- 433
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 33181171
- Full Text :
- https://doi.org/10.1016/j.jmb.2020.11.001