544605 Developing and Evaluating Integrated Metabolic Regulatory Models for Microbial Life

Sunday, October 14, 2018
Molly Creagar1, Thomas Kamp2, Ruby Fore3, Derek Friend4, Craig Disselkoen5, Christopher S. Henry6, Matthew DeJongh7, Aaron Best8, William Lindsey2 and Nathan Tintle9, (1)University of San Francisco, San Francisco, CA, (2)Dordt College, Sioux Center, IA, (3)Brown University, Providence, RI, (4)University of Nevada, Reno, Reno, NV, (5)University of California, San Diego, San Diego, CA, (6)Argonne National Laboratory, Argonne, IL, (7)Computer Science, Hope College, Holland, MI, (8)Biology, Hope College, Holland, MI, (9)Mathematics, Dordt College, Sioux Center, IA

A number of papers have described methods to include transcriptional regulatory networks (TRNs) in the development of metabolic models. However, in general, these models do not allow for statistical uncertainty in TRN interactions. Furthermore, methods which do allow for uncertainty do so in a non-rigorous manner which, effectively, downweights prior transcriptomics data to the point where it has little impact on the resulting model. To combat these limitations, we developed an integrated metabolic regulatory model (iMRM). This novel approach explicitly models the statistical uncertainty in gene state activity inferences by using gene activity state estimates, and the iMRM process measures the flux through reactions for a sole single-cell organism. This allows for benefits such as differential thresholds for gene activity for different genes, a stronger correlation with experimental flux data, and the application of a non-Boolean confidence metric. Furthermore, this is the first such metabolic model to be grounded on a statistically rigorous foundation.

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