Figure 5.

Overlay of Ifn-β timecourse analysis onto the macrophage pathway using BioLayout Express3D. Views of regions of the macrophage pathway where components were found to be regulated Ifn-β. Components regulated at the level of gene expression are enlarged and coloured according to their cluster membership. All non-regulated components and other nodes are grey. (a) Regulation of Toll Like Receptor Signalling. All endosomal TLRs, Myd88 and Tifa genes are induced from 1 h, their expression being maximally up-regulated at 4-8 h post-Ifn-β treatment. (b) Regulation of death-receptor and apoptosis signalling. The expression of all regulated components in this module rises from 1 h and reaches a maximum 2-4 h post-treatment. In contrast, the expression of the anti-apoptotic gene Bcl2 is suppressed at 4 h. (c) Regulation of the transcriptional targets of interferon signalling. 7 genes (shown in yellow) belong to cluster 2 and their expression induced from 1 h, becoming maximal at 4 h. 4 genes (in purple) were in cluster 3, with expression rising from 1 h and remaining maximal throughout 4-8 h post-treatment. Irf1 (in green) reaches maximal expression at 2 h. (d) Regulation of type I and type II interferon signalling. All receptor components, except Ifngr1, belong to clusters of induced genes. Socs1 and Socs3 are induced and reach maximal expression at early time points (1-2 or 2 h).

Raza et al. BMC Systems Biology 2010 4:63   doi:10.1186/1752-0509-4-63
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