CFN42 and 1021 bioinformatic transcriptional regulatory networks from culture and symbiosis.

CFN42 proteome-transcriptome mixed data of exponential growth and nitrogen-fixing bacteroids, as well as 1021 transcriptome data of growth and nitrogen-fixing bacteroids, were integrated into transcriptional regulatory networks (TRNs). The one-step construction network consisted of a matrix-clustering analysis of matrices of the gene profile and all matrices of the transcription factors (TFs) of their genome. The networks were constructed with the prediction of regulatory network application of the RhizoBindingSites database (http://rhizobindingsites.ccg.unam.mx/). The deduced free-living network contained 1,146 genes, including 380 TFs and 12 sigma factors. In addition, the bacteroid CFN42 network contained 884 genes, where 364 were TFs, and 12 were sigma factors, whereas the deduced free-living 1021 network contained 643 genes, where 259 were TFs and seven were sigma factors, and the bacteroid 1021 network contained 357 genes, where 210 were TFs and six were sigma factors. The similarity of these deduced condition-dependent networks and the biological and independent condition networks segregates from the random Erdös-Rényi networks. Deduced networks showed a low average clustering coefficient. They were not scale-free, showing a gradually diminishing hierarchy of TFs in contrast to the hierarchy role of the sigma factor in the K12 network. For rhizobia networks, partitioning the genome in the chromosome, chromids, and plasmids, where essential genes are distributed, and the symbiotic ability that is mostly coded in plasmids, may alter the structure of these deduced condition-dependent networks. It provides potential TF gen-target relationship data for constructing regulons, which are the basic units of a TRN.