From the transcriptional regulatory network of B. subtilis, we extracted the significant genes identified in the microarray condition, the TFs regulating their expression,

and the transcriptional interactions between TFs and their regulated genes. In these sub-networks, nodes represent genes and edges represent the transcriptional interactions. Known regulatory sites and transcriptional unit organization were obtained from DBTBS [45]. Identification of condition-specific modules We identified the LB+G/LB condition-specific modules applying to the condition specific sub-network, the methodology described in Resendis-Antonio et al [46] and this website Gutierrez-Rios et al [13]. Specifically, we clustered the genes based on their shortest distance within the network. Afterwards, we annotated each gene with its corresponding microarray expression level. The dendogram generated by the clustering algorithm was decomposed into modules and sub-modules. Hierarchical clustering algorithms produce a dendogram by iteratively joined pairs of data, with the closest 17DMAG cost correlation levels. We analyzed the distribution of correlation values, observing that ~90% (228 from 254) of the nodes in the dendogram have a correlation value greater than 80%. Hence, in order to isolate modules, we pruned every node with a correlation of less than

80% from the dendogram. In addition, to identifying sub-modules, we then pruned the dendogram once again; this time removing all the nodes with a correlation of less than 90%. Detection of orthologous genes A simple method for predicting the orthologous proteins present in two organisms is to selleck chemicals llc Phosphatidylethanolamine N-methyltransferase search for a pair of sequences, Xa in organism Ga and Xb in organism Gb, such that a search of the proteome of Gb with Xa indicates Xb to be the best hit. We made this comparison using the Blastp program [47, 48] with the E. coli and the B subtilis genome as input. If the protein in each genome has the highest E-value and an upper threshold of 10-5 in both genomes, we considered them to be orthologous. From this set we selected the significant expressed genes, published in our previous work run under the

same conditions of LB growth, in the presence or absence of glucose [13]. Clustering of microarray data of orthologous genes We applied a hierarchical centroid linkage clustering algorithm [49, 50] to the log ratios of the differences between the orthologous genes of E. coli and B. subtilis, with the correlation un-centered as a similarity measure… The clustering results were visualized using the Treeview program [51]. List of abbreviations CRE, SM, LB, LB+G, TF, PTS, B. subtilis, E. coli. Acknowledgements We thank Nancy Mena for technical support. I am in indebted to Antonio Loza for discussion and microarray selection. I also want to thank Enrique Merino for revising the final version of this manuscript. This work was supported by grant IN215808 from PAPIIT-UNAM and CONACyT-58840 to R.M.