An integrated framework to model cellular phenotype as a component of biochemical networks.
Document Type
Article
Publication Date
1-1-2011
Abstract
Identification of regulatory molecules in signaling pathways is critical for understanding cellular behavior. Given the complexity of the transcriptional gene network, the relationship between molecular expression and phenotype is difficult to determine using reductionist experimental methods. Computational models provide the means to characterize regulatory mechanisms and predict phenotype in the context of gene networks. Integrating gene expression data with phenotypic data in transcriptional network models enables systematic identification of critical molecules in a biological network. We developed an approach based on fuzzy logic to model cell budding in Saccharomyces cerevisiae using time series expression microarray data of the cell cycle. Cell budding is a phenotype of viable cells undergoing division. Predicted interactions between gene expression and phenotype reflected known biological relationships. Dynamic simulation analysis reproduced the behavior of the yeast cell cycle and accurately identified genes and interactions which are essential for cell viability.
Recommended Citation
Gormley, Michael; Akella, Viswanadha U; Quong, Judy N; and Quong, Andrew A, "An integrated framework to model cellular phenotype as a component of biochemical networks." (2011). Department of Cancer Biology Faculty Papers. Paper 44.
https://jdc.jefferson.edu/cbfp/44
PubMed ID
22190923
Comments
This article has been peer reviewed. It was published in: Advances in bioinformatics.
2011;2011:608295.
The published version is available at DOI: 10.1155/2011/608295. Copyright © Hindawi