Schwartz Jean-Marc, Gaugain Claire, Nacher Jose C, de Daruvar Antoine, Kanehisa Minoru
Bioinformatics Center, Kyoto University, Uji, Kyoto 611-0011, Japan.
Genome Biol. 2007;8(6):R123. doi: 10.1186/gb-2007-8-6-r123.
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.
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.
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.
高通量技术使可用生物数据的数量和类型成倍增加,首次实现对生物细胞生理学的全面理解已成为一个可实现的目标。这一目标需要整合不同尺度下的大量异构数据。尤其有必要将传统上对基因组数据的关注扩展到真正的功能关注上,即根据执行细胞生存所需功能的实际代谢过程来描述细胞的活性。
在这项工作中,我们提出了一种新的代谢分析方法,该方法使我们能够在基因组尺度上观察代谢功能的转录活性。这些功能通过基本模式来描述,借助模块化方法,可以在基因组尺度模型中计算这些基本模式。我们通过对酵母细胞应激的转录代谢反应进行详细分析,例证了这一新视角。基本模式分析与基因表达数据的整合使我们能够识别在不同应激条件下一些功能上被诱导或抑制的代谢过程。这些基本模式的组合导致了特定代谢主干的识别。
本研究为细胞尺度的代谢分析开辟了一个新框架,在这个框架中,可以根据整个过程而非单个基因来分析转录活性。我们还表明,活跃基本模式集呈现出高度不均衡的组织形式,其中大多数执行专门任务,而较小比例的模式执行多任务功能并主导一般应激反应。