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dc.contributor.advisorAlexander van Oudenaarden.en_US
dc.contributor.authorMettetal, Jerome Thomas, IIen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Physics.en_US
dc.date.accessioned2009-04-29T17:43:41Z
dc.date.available2009-04-29T17:43:41Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/45445
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Physics, 2008.en_US
dc.descriptionIncludes bibliographical references (p. 199-206).en_US
dc.description.abstractCells are not simple passive observers oblivious to their environment, but sense and adapt to environmental changes in order to thrive. In addition to sensing the presence of signals in the environment, cells can extract information relating to the dynamics and spatial location of these signals and implement a response to these extracellular perturbations. This work examines a variety of signal-processing and decision-making processes across several different organisms. To explore the connection between biological network topology and temporal signal processing, we study how periodic signals are propagated in the Hog1 osmotic response pathway of the budding yeast Saccharomyces cerevisiae. Utilizing systems identification tools from control engineering, we study how the cells rapidly and robustly maintain osmotic homeostasis. By measuring the expression level of key proteins we begin to understand how fluctuating environments regulate gene expression. The lac operon in Escherichia coli has the ability to display a bistable, "all-ornothing" response to sugar. To understand how noise drives transitions between these two stable states, we measure switching dynamics in a population of cells. A simple model is constructed that can make predictions about system behavior unavailable from a deterministic model. Further, by measuring individual switching events in a similar bistable system implemented in the Galactose utilization pathway of Saccharomyces cerevisiae, we find that correlations in switching times of related individuals can be explained in terms of correlations in levels of key regulatory proteins. Many single celled organisms, such as the slime mold Dictyostelium discoideum, can sense and respond to concentration gradients of extracellular signaling molecules. We find that the cells' ability to detect an extracellular signal is influenced by an asymmetric intracellular signal, which varies in direction and magnitude from cell-to-cell. Further, a model that accounts for both signals predicts the observed population response to directed stimuli.en_US
dc.description.abstract(cont.) Finally, we explore a "bet-hedging" strategy for fluctuating environments with an engineered population of Saccharomyces cerevisiae cells that randomly switch between two phenotypes. Each phenotype is fit to one of two alternating environments. We find that to optimize fitness, cells must tune the phenotypic transition rates in accordance with the rate of environmental transitions.en_US
dc.description.statementofresponsibilityby Jerome Thomas Mettetal, II.en_US
dc.format.extent206 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectPhysics.en_US
dc.titleSignal processing and decision making in single cellsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physics
dc.identifier.oclc318116978en_US


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