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