BACKGROUND: High-throughput techniques have multiplied the amount and the types of available biological data, and for the first time achieving a global comprehension of the physiology of biological cells has become an achievable goal. This aim requires the integration of large amounts of heterogeneous data at different scales. It is notably necessary to extend the traditional focus on genomic data towards a truly functional focus, where the activity of cells is described in terms of actual metabolic processes performing the functions necessary for cells to live. RESULTS: In this work, we present a new approach for metabolic analysis that allows us to observe the transcriptional activity of metabolic functions at the genome scale. These functions are described in terms of elementary modes, which can be computed in a genome-scale model thanks to a modular approach. We exemplify this new perspective by presenting a detailed analysis of the transcriptional metabolic response of yeast cells to stress. The integration of elementary mode analysis with gene expression data allows us to identify a number of functionally induced or repressed metabolic processes in different stress conditions. The assembly of these elementary modes leads to the identification of specific metabolic backbones. CONCLUSION: This study opens a new framework for the cell-scale analysis of metabolism, where transcriptional activity can be analyzed in terms of whole processes instead of individual genes. We furthermore show that the set of active elementary modes exhibits a highly uneven organization, where most of them conduct specialized tasks while a smaller proportion performs multi-task functions and dominates the general stress response.
BACKGROUND: High-throughput techniques have multiplied the amount and the types of available biological data, and for the first time achieving a global comprehension of the physiology of biological cells has become an achievable goal. This aim requires the integration of large amounts of heterogeneous data at different scales. It is notably necessary to extend the traditional focus on genomic data towards a truly functional focus, where the activity of cells is described in terms of actual metabolic processes performing the functions necessary for cells to live. RESULTS: In this work, we present a new approach for metabolic analysis that allows us to observe the transcriptional activity of metabolic functions at the genome scale. These functions are described in terms of elementary modes, which can be computed in a genome-scale model thanks to a modular approach. We exemplify this new perspective by presenting a detailed analysis of the transcriptional metabolic response of yeast cells to stress. The integration of elementary mode analysis with gene expression data allows us to identify a number of functionally induced or repressed metabolic processes in different stress conditions. The assembly of these elementary modes leads to the identification of specific metabolic backbones. CONCLUSION: This study opens a new framework for the cell-scale analysis of metabolism, where transcriptional activity can be analyzed in terms of whole processes instead of individual genes. We furthermore show that the set of active elementary modes exhibits a highly uneven organization, where most of them conduct specialized tasks while a smaller proportion performs multi-task functions and dominates the general stress response.
Authors: Roland Barriot; Jérôme Poix; Alexis Groppi; Aurélien Barré; Nicolas Goffard; David Sherman; Isabelle Dutour; Antoine de Daruvar Journal: Nucleic Acids Res Date: 2004-07-07 Impact factor: 16.971
Authors: M Juanita Martinez; Sushmita Roy; Amanda B Archuletta; Peter D Wentzell; Sonia Santa Anna-Arriola; Angelina L Rodriguez; Anthony D Aragon; Gabriel A Quiñones; Chris Allen; Margaret Werner-Washburne Journal: Mol Biol Cell Date: 2004-09-29 Impact factor: 4.138
Authors: Frank Wessely; Martin Bartl; Reinhard Guthke; Pu Li; Stefan Schuster; Christoph Kaleta Journal: Mol Syst Biol Date: 2011-07-19 Impact factor: 11.429
Authors: Nathan L Tintle; Aaron A Best; Matthew DeJongh; Dirk Van Bruggen; Fred Heffron; Steffen Porwollik; Ronald C Taylor Journal: BMC Bioinformatics Date: 2008-11-05 Impact factor: 3.169