Criticality-driven enhancer-promoter dynamics in Drosophila chromosomes
Ganesh, G.; Fiche, J.-B.; Nöllmann, M.; Mozziconacci, J.
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Recent live imaging in Drosophila embryonic nuclei revealed frequent enhancer-promoter (E-P) contacts across megabase-scale distances, challenging classical polymer models. To identify the physical mechanisms enabling such long-range communication, we performed coarse-grained polymer simulations exploring three chromatin organization modes: ideal polymers, loop extrusion, and compartmental segregation. We found that compartmental segregation, when tuned near the coil-globule phase transition, best captured the experimentally observed structure and dynamics. Adding loop extrusion further improved the agreement with experimental data, suggesting a synergistic interplay. These results indicate that Drosophila chromatin folds near a critical point, enabling dynamic E-P interactions over long distances. Our findings provide a mechanistic framework for chromatin architecture during development and point to criticality as a potentially universal principle of genome organization.
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