Distinct polymer physics principles govern chromatin dynamics in mouse and Drosophila topological domains.

Fiche publication


Date publication

août 2015

Journal

BMC genomics

Auteurs

Membres identifiés du Cancéropôle Est :
Dr SEXTON Thomas


Tous les auteurs :
Ea V, Sexton T, Gostan T, Herviou L, Baudement MO, Zhang Y, Berlivet S, Le Lay-Taha MN, Cathala G, Lesne A, Victor JM, Fan Y, Cavalli G, Forné T

Résumé

In higher eukaryotes, the genome is partitioned into large "Topologically Associating Domains" (TADs) in which the chromatin displays favoured long-range contacts. While a crumpled/fractal globule organization has received experimental supports at higher-order levels, the organization principles that govern chromatin dynamics within these TADs remain unclear. Using simple polymer models, we previously showed that, in mouse liver cells, gene-rich domains tend to adopt a statistical helix shape when no significant locus-specific interaction takes place.

Mots clés

Animals, Chromatin, chemistry, Chromatin Assembly and Disassembly, DNA, chemistry, Drosophila melanogaster, genetics, Epigenesis, Genetic, Liver, metabolism, Mice, Models, Molecular, Models, Statistical, Mouse Embryonic Stem Cells, cytology, Nucleic Acid Conformation

Référence

BMC Genomics. 2015 Aug 15;16:607