2007 APS March Meeting
Volume 52, Number 1
Monday–Friday, March 5–9, 2007;
Denver, Colorado
Session B5: Adaptation in Biological Systems
11:15 AM–1:39 PM,
Monday, March 5, 2007
Colorado Convention Center
Room: Korbel 1A-1B
Sponsoring
Unit:
DBP
Chair: Ned Wingreen, Princeton University
Abstract ID: BAPS.2007.MAR.B5.3
Abstract: B5.00003 : Adaptation by Plasticity of Genetic Regulatory Networks
12:27 PM–1:03 PM
Preview Abstract
Abstract
Author:
Naama Brenner
(Technion - Israel Institute of Technology)
Genetic regulatory networks have an essential role in adaptation and
evolution of cell populations. This role is strongly related to their
dynamic properties over intermediate-to-long time scales. We have used the
budding yeast as a model Eukaryote to study the long-term dynamics of the
genetic regulatory system and its significance in evolution. A continuous
cell growth technique (chemostat) allows us to monitor these systems over
long times under controlled condition, enabling a quantitative
characterization of dynamics: steady states and their stability, transients
and relaxation. First, we have demonstrated adaptive dynamics in the \textit{GAL}
system, a classic model for a Eukaryotic genetic switch, induced and
repressed by different carbon sources in the environment. We found that both
induction and repression are only transient responses; over several
generations, the system converges to a single robust steady state,
independent of external conditions. Second, we explored the functional
significance of such plasticity of the genetic regulatory network in
evolution. We used genetic engineering to mimic the natural process of gene
recruitment, placing the gene \textit{HIS3} under the regulation of the \textit{GAL} system. Such
genetic rewiring events are important in the evolution of gene regulation,
but little is known about the physiological processes supporting them and
the dynamics of their assimilation in a cell population. We have shown that
cells carrying the rewired genome adapted to a demanding change of
environment and stabilized a population, maintaining the adaptive state for
hundreds of generations. Using genome-wide expression arrays we showed that
underlying the observed adaptation is a global transcriptional programming
that allowed tuning expression of the recruited gene to demands. Our results
suggest that non-specific properties reflecting the natural plasticity of
the regulatory network support adaptation of cells to novel challenges and
enhance their evolvability.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2007.MAR.B5.3