APS March Meeting 2017
Volume 62, Number 4
Monday–Friday, March 13–17, 2017;
New Orleans, Louisiana
Session F4: Physics of Genome Organization: from DNA to Chromatin I
11:15 AM–2:15 PM,
Tuesday, March 14, 2017
Room: 263
Sponsoring
Units:
DBIO GSNP
Chair: Alexandre Morozov, Rutgers University
Abstract ID: BAPS.2017.MAR.F4.7
Abstract: F4.00007 : The "self-stirred" genome: Bulk and surface dynamics of the~chromatin globule
12:51 PM–1:27 PM
Preview Abstract
Abstract
Author:
Alexandra Zidovska
(Center for Soft Matter Research, Department of Physics, New York University)
Chromatin structure and dynamics control all aspects of DNA biology yet are
poorly understood. In interphase, time between two cell divisions, chromatin
fills the cell nucleus in its minimally condensed polymeric state. Chromatin
serves as substrate to a number of biological processes, e.g. gene
expression and DNA replication, which require it to become locally
restructured. These are energy-consuming processes giving rise to
non-equilibrium dynamics. Chromatin dynamics has been traditionally studied
by imaging of fluorescently labeled nuclear proteins and single DNA-sites,
thus focusing only on a small number of tracer particles. Recently, we
developed an approach, displacement correlation spectroscopy (DCS) based on
time-resolved image correlation analysis, to map chromatin dynamics
simultaneously across the whole nucleus in cultured human cells [1]. DCS
revealed that chromatin movement was coherent across large regions (4--5$\mu
$m) for several seconds. Regions of coherent motion extended beyond the
boundaries of single-chromosome territories, suggesting elastic coupling of
motion over length scales much larger than those of genes [1]. These
large-scale, coupled motions were ATP-dependent and unidirectional for
several seconds. Following these observations, we developed a hydrodynamic
theory of active chromatin dynamics, using the two-fluid model and
describing the content of cell nucleus as a chromatin solution, which is
subject to both passive thermal fluctuations and active (ATP-consuming)
scalar and vector events [2]. In this work we continue in our efforts to
elucidate the mechanism and function of the chromatin dynamics in
interphase. We investigate the chromatin interactions with the nuclear
envelope and compare the surface dynamics of the chromatin globule with its
bulk dynamics.
[1] Zidovska A, Weitz DA, Mitchison TJ, \textit{PNAS,~}110 (39), 15555, 2013
[2] Bruinsma R, Grosberg AY, Rabin Y, Zidovska A, \textit{Biophys. J.,}~106 (9), 1871, 2014
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2017.MAR.F4.7