2008 APS March Meeting
Volume 53, Number 2
Monday–Friday, March 10–14, 2008;
New Orleans, Louisiana
Session A7: Oscillations Without Transcription in Vivo and in Vitro
8:00 AM–11:00 AM,
Monday, March 10, 2008
Morial Convention Center
Room: RO5
Sponsoring
Units:
DBP GSNP
Chair: Michal Zochowski, University of Michigan
Abstract ID: BAPS.2008.MAR.A7.4
Abstract: A7.00004 : Stability and Noise in the Cyanobacterial Circadian Clock
9:48 AM–10:24 AM
Preview Abstract
Abstract
Author:
Irina Mihalcescu
(Universit\'e Joseph Fourier - Grenoble)
Accuracy in cellular function has to be achieved despite random
fluctuations
(noise) in the concentrations of different molecular constituents
inside and
outside the cell. Single cell in vivo monitoring reveals that
individual
cells generate autonomous circadian rhythms in protein abundance. In
multi-cellular organisms, the individual cell rhythms appear to
be noisy
with drifting phases and frequencies. However, the whole organism is
significantly more accurate, the temporal precision being
achieved most
probably via intercellular coupling of the individual noisy
oscillators.
In cyanobacteria, we have shown that single cell oscillators are
impressively stable and a first estimation rules out strong
intercellular
coupling. Interestingly, these prokaryotes also have the simplest
molecular
mechanism at the heart of their circadian clock. In the absence of
transcriptional activity in vivo, as well alone in vitro, the
three clock
proteins KaiA, KaiB and KaiC generate a self-sustained circadian
oscillation
of autophosphorylation and dephosphorylation. Recent chemical
kinetics
models provide a possible understanding of the three-protein
oscillator, but
the measured in vivo stability remains yet unexplained. Is the clock
stability a built-in property for each bacterium or does a weak
intercellular coupling, make them appear like that?
To address this question we first theoretically designed our
experiment to
be able to distinguish coupling, even weak, from phase diffusion.
As the
precision of our evaluation increases with the length of the
experiments, we
continuously monitor, for a couple of weeks, mixtures of cell
populations
with different initial phases. The inherent experimental noise
contribution,
initially dominant, is reduced by enhanced statistics. In
addition, in situ
entrainment experiments confirm our ability to detect a coupling
of the
circadian oscillator to an external force and to describe
explicitly the
dynamic change of the mean phase. We report a value of the
coupling constant
that is small compared to the diffusion constant. These results
therefore
confirm that the cyanobacterial clock stability is a built-in
property: the
cyanobacterian clock mechanism is not only the simplest but also
the most
robust.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2008.MAR.A7.4