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Chromatin topology is coupled to Polycomb group protein subnuclear organization.
- Source :
-
Nature communications [Nat Commun] 2016 Jan 13; Vol. 7, pp. 10291. Date of Electronic Publication: 2016 Jan 13. - Publication Year :
- 2016
-
Abstract
- The genomes of metazoa are organized at multiple scales. Many proteins that regulate genome architecture, including Polycomb group (PcG) proteins, form subnuclear structures. Deciphering mechanistic links between protein organization and chromatin architecture requires precise description and mechanistic perturbations of both. Using super-resolution microscopy, here we show that PcG proteins are organized into hundreds of nanoscale protein clusters. We manipulated PcG clusters by disrupting the polymerization activity of the sterile alpha motif (SAM) of the PcG protein Polyhomeotic (Ph) or by increasing Ph levels. Ph with mutant SAM disrupts clustering of endogenous PcG complexes and chromatin interactions while elevating Ph level increases cluster number and chromatin interactions. These effects can be captured by molecular simulations based on a previously described chromatin polymer model. Both perturbations also alter gene expression. Organization of PcG proteins into small, abundant clusters on chromatin through Ph SAM polymerization activity may shape genome architecture through chromatin interactions.
- Subjects :
- Amino Acid Motifs
Animals
Cell Line
Chromatin Immunoprecipitation
Drosophila
Fluorescent Antibody Technique
Microscopy
Molecular Dynamics Simulation
Optical Imaging
Polycomb-Group Proteins metabolism
Polymers
Protein Structure, Quaternary
Reverse Transcriptase Polymerase Chain Reaction
Sequence Analysis, DNA
Sequence Analysis, RNA
Chromatin metabolism
DNA-Binding Proteins metabolism
Drosophila Proteins metabolism
Intranuclear Space metabolism
Polycomb Repressive Complex 1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 26759081
- Full Text :
- https://doi.org/10.1038/ncomms10291