Condensed Chromatin Behaves like a Solid on the Mesoscale In Vitro and in Living Cells
Author(s) -
Hilmar Strickfaden,
Thomas O. Tolsma,
Ajit Kumar Sharma,
D. Alan Underhill,
Jeffrey C. Hansen,
Michael J. Hendzel
Publication year - 2020
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.11.027
Subject(s) - chromatin , euchromatin , heterochromatin , biology , histone , nucleosome , scaffold/matrix attachment region , dna , microbiology and biotechnology , biophysics , chia pet , bivalent chromatin , histone modifying enzymes , chip sequencing , chromatin remodeling , genetics
The association of nuclear DNA with histones to form chromatin is essential for temporal and spatial control of eukaryotic genomes. In this study, we examined the physical state of condensed chromatin in vitro and in vivo. Our in vitro studies demonstrate that self-association of nucleosomal arrays under a wide range of solution conditions produces supramolecular condensates in which the chromatin is physically constrained and solid-like. By measuring DNA mobility in living cells, we show that condensed chromatin also exhibits solid-like behavior in vivo. Representative heterochromatin proteins, however, display liquid-like behavior and coalesce around the solid chromatin scaffold. Importantly, euchromatin and heterochromatin show solid-like behavior even under conditions that produce limited interactions between chromatin fibers. Our results reveal that condensed chromatin exists in a solid-like state whose properties resist external forces and create an elastic gel and provides a scaffold that supports liquid-liquid phase separation of chromatin binding proteins.
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