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Open AccessHighly AccessResearch article

Aggregation of topological motifs in the Escherichia coli transcriptional regulatory network

Radu Dobrin1 email, Qasim K Beg1 email, Albert-László Barabási2 email and Zoltán N Oltvai1 email

Department of Pathology, Northwestern University, Chicago, IL 60611, USA

Department of Physics, University of Notre Dame, Notre Dame, IN 46556, USA

author email corresponding author email

BMC Bioinformatics 2004, 5:10doi:10.1186/1471-2105-5-10

Published: 30 January 2004

Abstract

Background

Transcriptional regulation of cellular functions is carried out through a complex network of interactions among transcription factors and the promoter regions of genes and operons regulated by them.To better understand the system-level function of such networks simplification of their architecture was previously achieved by identifying the motifs present in the network, which are small, overrepresented, topologically distinct regulatory interaction patterns (subgraphs). However, the interaction of such motifs with each other, and their form of integration into the full network has not been previously examined.

Results

By studying the transcriptional regulatory network of the bacterium, Escherichia coli, we demonstrate that the two previously identified motif types in the network (i.e., feed-forward loops and bi-fan motifs) do not exist in isolation, but rather aggregate into homologous motif clusters that largely overlap with known biological functions. Moreover, these clusters further coalesce into a supercluster, thus establishing distinct topological hierarchies that show global statistical properties similar to the whole network. Targeted removal of motif links disintegrates the network into small, isolated clusters, while random disruptions of equal number of links do not cause such an effect.

Conclusion

Individual motifs aggregate into homologous motif clusters and a supercluster forming the backbone of the E. coli transcriptional regulatory network and play a central role in defining its global topological organization.


© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.