ChemE Fall Seminar Series
Engineered Gene Circuits
Jeff Hasty
Department of Bioengineering
Institute for Nonlinear Science
University of California, San Diego
Friday, September 21, 2007
3:00pm, 66-110
(Refreshments will be served at 2:45pm)
Everyone is invited!
Uncovering the structure and function of gene regulatory networks has become
one of the central challenges of the post-sequencing era. Theoretical models
of protein-DNA feedback loops and gene regulatory networks have long been
proposed, and recently, certain qualitative features of such models have
been experimentally corroborated. For the first portion of the presentation,
recent progress in constructing two synthetic gene oscillators will be
discussed. These oscillators were built in accordance with design criteria
that was developed with computational modeling. Both oscillators are robust,
with all cells oscillating with a characteristic frequency that can be tuned
with external inducers or temperature shifts. In the second part of the
presentation, the response of metabolic gene regulation to periodic changes
in the external carbon source will be discussed. The central finding is the
metabolic regulatory system acts as a low-pass filter that reliably responds
to a slowly changing environment, while effectively ignoring fluctuations
that are too fast for the cell to mount an efficient response. Computational
modeling calibrated with experimental data is used to determine that
frequency selection in the system is controlled by the interaction of
coupled positive feedback networks governing the signal transduction of
alternative carbon sources. The simulations suggest that the feedback loops
may confer a robustness to environmental fluctuations on cells regardless of
deficiencies in network components. This prediction is validated with an
experimental comparison of two cellular strains that exhibit the same
filtering properties despite having markedly different induction
characteristics. The underlying methodology highlights the utility of
engineering-based methods in the exploration of gene regulatory networks.