| Literature DB >> 16986625 |
N Yalamanchili1, D E Zak, B A Ogunnaike, J S Schwaber, A Kriete, B N Kholodenko.
Abstract
Large, complex data sets that are generated from microarray experiments, create a need for systematic analysis techniques to unravel the underlying connectivity of gene regulatory networks. A modular approach, previously proposed by Kholodenko and co-workers, helps to scale down the network complexity into more computationally manageable entities called modules. A functional module includes a gene's mRNA, promoter and resulting products, thus encompassing a large set of interacting states. The essential elements of this approach are described in detail for a three-gene model network and later extended to a ten-gene model network, demonstrating scalability. The network architecture is identified by analysing in silico steady-state changes in the activities of only the module outputs, communicating intermediates, that result from specific perturbations applied to the network modules one at a time. These steady-state changes form the system response matrix, which is used to compute the network connectivity or network interaction map. By employing a known biochemical network, the accuracy of the modular approach and its sensitivity to key assumptions are evaluated.Mesh:
Substances:
Year: 2006 PMID: 16986625 PMCID: PMC2346590 DOI: 10.1049/ip-syb:20050090
Source DB: PubMed Journal: Syst Biol (Stevenage) ISSN: 1741-2471